Table Of Content

Volume 14, 1999 Index Author Index Abe, T, 249, 687 Camfield, P, 617 Elpeleg, ON, 479 Houri, S, 479 Adesina, AM, 411 Campistol, J, 683 El-Schahawi, M, 610 Hove, MT, 621 Akalin, T, 745 Campos, Y, 131 Elwan, MA, 265 Hsiung, G-YR, 268 Akar, E, 749 Capovilla, G, 395, 446 Engel, AG, 38 Hsu, HW, 473 Akar, N, 749 Carollo, C, 352 Engle, E, 34 Huseyinov, A, 418 Albright, AL, 408 Carratala, F, 683 Erzen, C, 678 Hwang, P, 304 Aldenkamp, AP, 795 Carroll, A, 801 Espeel, M, 434 Hyland, K, 529, S9 Alder, J, 574 Carter, LP, 67 Eviatar, L, 490 Alehan, FK, 130 Caruso, JM, 428 Ewing-Cobbs, L, 496 Ibarra, R, 88 Alikasifoglu, M, 159 Castro-Gago, M, 131, 824 Iglesias-Diz, M, 824 Alonso, A, 131 Catsman-Berrevoets, CE, 243 Falcini, F, 363 Imai, K, 756 Alper, G, 678 Cavalier, L, 660 Farmer, PM, 123 Inagaki, M, 422 Alshansky, A, 490 Chabot, RJ, 343 Fattal-Valevski, A, 724 Incorpora, G, 196 Al-Sulaiman, A, 295 Chace, DH, $4 Feldman-Winter, L, 479 Inui, K, 756 Amat, L, 434 Chalmers, A, 478 Fennell, E, 368, 592, 642 Ishikawa, Y, 168 Anar, B, 159 Chance, PF, 43, 660 Fernandez Alvarez, E, 683 Ismail, H, 295 Andermann, E, 565 Chee, CM, 696 Ferri, R, 446 Andermann, F, 554, 565 Chez, MG, 239 Fiumara, A, 550 Jackson, AH, 464 Anderson, A, 502 Chiarelli, F, 746 Flitman, HP, 473 Jaeken, J, 728 Anlar, B, 198 Chiba, S, 471 Fontaine, S, 565 Jaffa, A, 724 Antony, JH, 815 Chiodo, S, 113 Frank, Y, 277 Janisch, C, 467 Apak, RA, 198 Christodoulou, J, 162, 518 Freeman, JM, 469 Jay, V, 83 Applegarth, DA, 464 Chudnow, R, 272 Frye, VH, 388 Jaynes, M, 325, 341, 481 Aracil, A, 434 Chun, RWM, 1 Fujii, T, 265 Joubert, M, 554, 565 Arenas, J, 131 Chusid, R, 277 Fukuyama, Y, 26 Arends, J, 795 Cimaz, R, 363 Fyfe, S, 440 Kaga, M, 118, 422 Arikan, ©, 678 Clementi, M, 352 Kalra, V, 541 Arnold, LA, S9 Coakley, JC, 518 Gabreéls, F, 37, 728 Kanakoudi, FG, 480 Arpino, C, 151 Comair, YG, 15 Gabreéls-Festin, A, 52 Kandt, RS, 401 Auerbach, JG, 299 Comi, AM, 388 Gale, S, 636 Kapaun, P, 222 Autret, A, 144 Conill, J, 434 Garozzo, R, 266 Kaplan, AM, 673 Awaad, Y, 75, 316, 781 Corcia, P, 144 Gartside, PS, 602 Katzos, GS, 480 Coutinho, LMB, 467 Gascon, GG, 207 Kawashima, K, 265 Bademosi, 0, 295 Coyne, MF, 781 Gawehn, J, 451 Khajavi, K, 15 Bagan, BT, 239 Crawford, G, 343 Gay, CT, 341 Ko, TS, 282 Bandy, DJ, 673 Crawley, A, 304 Geng, S, 745 Koenig, M, 660 Bandyopadhyay, S, 685 Creten, WL, 243 Gerez, M, 88 Kohlschiietter, A, 222 Banwell, BL, 83 Curatolo, P, 136, 151, 446, 618 Ghosh, D, 337, 339 Kontopoulos, EE, 289, 480, 514 Barkovich, AJ, 628 Gilbert, DL, 469, 597, 602 Kornreich, L, 331 Barnard, C, 787 D’Agata, M, 547 Gillet, P, 144 Kose, G, 198 Barone, R, 550 Darras, BT, 620 Gingold, MK, 325, 481, 482 Kramer, U, 485 Barr, J, 732 D’Asero, G, 550 Giros, M, 434 Kraynack, NC, 754 Barthez, MA, 144 Dean, DE, 98 Gitten, J, 368, 592, 642 Kremenopoulos, GM, 514 Barzilai, A, 732 de Courten-Myers, GM, 98, 473 Glauser, TA, 382, 597, 602 Kunkel, L, 33 Battistella, A, 352 Deda, G, 749 Goebel, HH, 30 Kuppusamy, K, 78 Bauer, L, 229 Dede, D, 368, 592, 642 Goldberg, S, 649 Kurahashi, H, 756 Baumgartner, J, 496 de Menezes, MS, 268 Gombakis, NP, 480 Kure, S, 464, 728 Baxter, D, 229 Desnick, RJ, 543 Gordon, RE, 78 Kuroki, S, 711 Beaty, BJ, 1 de Toffol, B, 144 Granitzny, B, 222 Kutai, M, 724 Beccaria, F, 395 De Vivo, DC, $1, $23 Graveline, C, 304 Kutukculer, N, 418 Becker, LE, 83 Devoti, M, 357 Greco, R, 746 Beiras-Igiesias, A, 131 Dickstein, DP, 207 Grond, M, 543 Lahat, E, 732 Berg, BO, 736 Dilenge, M-E, 509 Gross-Tsur, V, 299 Landau, YE, 299 Bergqvist, AGC, 696 DiMario, FJ, 401 Grueneich, R, 78 Landry, S, 502 Berkovitch, M, 732 DiMario, FJ Jr, 229, 533 Gupta, S, 203 Lane, JB, 524 Billard, C, 144 DiMauro, S, 610, S23 Langsford, S, 801 Biondi, R, 446 Dinh, L, 509 Haacke, M, 78 Lanska, DJ, 337 Birnkrant, DJ, 139 Dittmann, RW, 222 Haftel, L, 479 Laverda, AM, 352 Black, FH, 772 Dizdarer, G, 418 Hahn, JF, 15 Law, PA, 388 Bodensteiner, JB, 271, 325, 481 Dobyns, WB, 660 Hamano, K, 711 Lawson, MA, 673 Boduroglu, K, 159 Dodge, PR, 537, 620 Hammer, MS, 239 Leary, M, 751 Boltshauser, E, 583 Domizio, S, 746 Hancock, E, 71 Lee, BCP, 78 Bone, G, 304 Douglas, G, 801 Harel, S, 724 Lee, JK, 282 Bonilla, E, $23 Dubowitz, V, 26 Harris, MJ, 343 Leech, RW, 67, 136, 271 Boénnemann, CG, 31 Duchowny, M, 759 Hatten, ME, 574 Leitner, Y, 724 Bonstelle, CT, 673 Dye, D, 440 Hecox, KE, 156 Leonard, H, 162, 440 Boor, R, 451 Heiss, W-D, 543 Leonard, S, 440 Bornholt, L, 772 Ebinger, F, 451 Hemingway, C, 751 Lerman, P, 820 Britton, BH, 67 Ehlers, JAC, 467 Hendy, J, 772 Lerman-Sagie, T, 331, 479, 818, 820 Brooks-Kayal, AR, 696 Eiben, RM, 139 Herndon, RM, 275 Levy, HL, 464 Brown, WD, 428 Eickhoff, W, 222 Hetherington, H, 524 Lieberman, D, 724 Brumback, A, 202 Eiris-Punal, J, 131, 824 Higgins, G, 162 Limperopoulos, C, 702 Brumback, RA, 67, 482, 617 Eisenring, J-J, 554 Hobbs, GR, 614 Lin, W, 78 Brunquell, P, 533 Ekinci, G, 678 Holden, KR, 708 Loeffel, M, 239 Buist, NMR, 529 Elgamal, A, 781 Hommet, C, 144 Lopez, L, 618 Bujanover, Y, 818 El-Ghazzawy, O, 78 Horikawa, M, 329 Lorberboym, M, 818 Burde, R, 649 Elia, M, 446 Hostoffer, RW, 754 Lotz, BP, 156 Butler, IJ, 137 Ellaway, C, 162 Houghton, S, 801 Lourmiere, JM, 144 826 Journal of Child Neurology / Volume 14, Number 12, December 1999 Luescher, JL, 642 Osborn, JP, 71 Rosenblatt, B, 702 Titanic-Schefft, M, 382 Lutchka, LM, 696 O’Tuama, LA, 207 Rossi, PG, 113, 547 Titus, MO, 708 Ouvrier, R, 53, 772 Rubboli, G, 395 Toda, T, 711 Magboll, G, 295 Overweg-Plandsoen, WCG, 795 Rudolf, J, 543 Tomer, A, 724 Majnemer, A, 702 Ozonoff, S, 636 Ruiz, M, 434 Tominaga, K, 329 Malkin, E, 610 Ozyiirek, R, 745 Russell, EC, 130 Toone, JR, 464 Mallet, A, 88 Rust, RS, 1 Topaloglu, H, 198 Mancias, P, 137 Palaksha, HK, 541 Ryan, MM, 815 Torres, OA, 529 Mandich, M, 614 Palmer, J, 15 Ryan, SG, 58, 187 Tran, TX, 583 Mano, T, 756 Palmer, SC, 583 Trifiletti, RR, 196, 266 Manson, J, 108 Pampols, T, 434 Sabatino, G, 746 Tsikoulas, I, 289, 514 Manwaring, KH, 673 Pan, JW, 534 Sakuragawa, N, 265 Tuncbilek, E, 159 Many, A, 724 Paquier, PF, 243 Santini, JJ, 144 Turanli, G, 198 Marcus, JC, 337 Parano, E, 196, 266 Santos, CS, 822 Tusa, RJ, 621 Maria, BL, 368, 553, 583, 592, 628, 642 Paret, G, 732 Santucci, M, 113 Tutuncuoglu, S, 418 Marzullo, E, 550 Parmeggiani, A, 113, 547 Satran, D, 660 Tiitiitiinciioglu, S, 745 Matthews, CG, 1 Patterson, MC, S16 Scaduto, MC, 113 Matucci-Cerinic, M, 363 Pavia, C, 434 Schanen, NC, 806 Vajsar, J, 83 Maytal, J, 490 Pavlakis, SG, 277 Schindler, D, 543 Van Campen, LE, 67 McAbee, G, 479 Pavone, L, 550 Schlegal, B, 751 van der Knaap, MS, 728 Meletti, S, 395 Pavone, P, 196, 266 Schochet, SS, 325 Van der Meere, J, 299 Melki, J, 43 Peeden, JN, 388 Schreier, HA, 480 Van Dongen, HR, 243 Mendel, RC, 67 Pellegri, A, 151 Seidel, WT, 716 van Mourik, M, 243 Meng, SZ, 377 Pellegrino, JE, 660 Serfontein, G, 343 van Raaij-Selten, B, 728 Mikulis, D, 304 Pellock, JM, 130 Serrano, C, 88 Van Tassel, P, 708 Millen, KJ, 574 Percy, AK, 256, 524 Shalev, RS, 299 Veggiotti, P, 395 Miller, JN, 636 Perilongo, G, 352 Shanske, A, 649 Verhoeven, NM, 728 Miller, RG, 173 Petetot, JM-C, 98 Shanske, S, 610 Verrotti, A, 746 Miller, VS, 529 Pineda, M, 434 Shelton, F de NAP, 619 Vining, EPG, 469 Millonig, JH, 574 Pintos-Martinez, E, 131 Shenoy, S, 271 Viahov, D, 151 Mimouni, M, 331 Pipitone, E, 547 Sheth, RD, 156, 334, 614, 685 Vossler, DG, 282 Minami, R, 168 Pippenger, CE, 382 Shevell, M, 509, 702 Mitchell, WG, 716 Platania, N, 196 Shikolka, C, 304 Waclawik, AJ, 156 Mitra, N, 123 Plioplys, AV, 203 Shtilbans, A, 610 Wade, S, 304 Moldavsky, M, 818 Poo, P, 683 Shultz, BL, 408 Walker, K, 751 Moras, P, 352 Pope, JF, 139 Shuper, A, 331 Wall, M, 801 Morgese, G, 746 Posar, A, 113, 547 Siddique, Q, 490 Wanders, RJA, 434 Morris, HH, 15 Powell, L, 801 Singh, R, 108 Watanabe, T, 249 Moser, A, 434 Pradhan, S, 337, 339 Sipahi, T, 749 West, J, 801 Moser, HW, 434 Prasad, MR, 496 Smith, K, 502 Wevers, RA, 728 Moss, SD, 673 Ptito, A, 565 Sofia, V, 446 White, JR, 822 Munoz, S, 75 Pullarkat, RK, 123 Spataro, J, 673 Whiting, K, 801 Murgia, A, 352 Puri, V, 233 Spinella, GM, 667 Whiting, S, 759 Musumeci, O, 610 Pyzik, PL, 469 Stanek, J, 473 Wilcken, B, 162 Musumeci, SA, 446 Stazi, MA, 151 Wildin, S, 502 Quisling, RG, 368, 628 Strober, JB, 691 Williams, AJ, 518 Naitoh, H, 422 Stronks, DL, 243 Williams, BJ, 636 Naylor, EW, S4 Rabinowicz, T, 98 Sugai, K, 422 Williams, K, 162 Neeper, R, 207 Rachmel, A, 331 Sumitani, S, 168 Wilson, DA, 67 Neumaier-Probst, E, 222 Rapin, I, 649 Sutherland, GR, 108 Wingate, RJT, 574 Newsom-Davis, J, 41 Raucher, A, 818 Swank, P, 502 Wirrell, E, 787 Nigro, M, 75 Raynes, HR, 649 Sy-Kho, R, 490 Wisniewski, KE, 123 Nihei, K, 422 Reiman, EM, 673 Wulbrand, H, 222 Nissenkorn, A, 818 Reitter, B, 451 Tachi, N, 471 Wyllie, E, 15 Northrup, H, 401 Richards, SD, 614 Takashima, S, 377 Novak, GP, 490 Riggs, G, 233 Takayama, S, 422 Yachnis, AT, 368, 570, 655 Novo-Rodriguez, MI, 131 Riggs, JE, 334 Tal-Posener, E, 724 Yamada, T, 329 Nowinski, C, 239 Riordan, G, 751 Tam, DA, 478 Yilmaz, Y, 678 Nunes, ML, 467 Ritchie, S, 614 Tassinari, CA, 395 Yoshida, S, 329 Riva, D, 357 Tayem, H, 781 Yoshikawa, H, 249, 687 Oda, Y, 249, 687 Roach, ES, 401 Taylor, GP, 83 Yoshioka, M, 711 Ohya, K, 471 Robb, JP, 554 Tchervenkov, C, 702 Okada, S, 756 Robin, NH, 754 Tekgiil, H, 418, 745 Zafeiriou, DI, 289, 480, 515 Okinaga, T, 756 Roels, F, 434 Tello, A, 88 Zander, A, 222 Oksel, F, 745 Rohlicek, C, 702 Tennekoon, GI, 691 Zeharia, A, 331 Ono, J, 756 Rorke, LB, 570, 655 Teylar, G, 678 Ziegler, DK, 482 Orgill, AA, 343 Rosainz, LC, 368 Tezcan, K, 533 Zimmerman, AW, 388 Orsal, A, 749 Rose, AL, 123 Thompson, WH, 1 Zulian, F, 363 Subject Index Abdominal cerebrospinal fluid Acute inflammatory polyneuropa- Adhalin, 27 Alacrima, 331-333 pseudocyst, 329-331 thy, 53-55 ADHD, 187, 192, 212-213, Alexander's disease, 275-276, Absence seizures, 61-62, 746-748 Acute necrotizing encephalopa- 299-302, 343-350, 801-805 325-329 Acetylcholine, 38-41 thy, 249-255 Adolescents, 144-149, 341 “Alice in Wonderland” syndrome, a-N-Acetylgalactosaminidase Acute spinal cord infarction, Adrenocortical insufficiency, 732-734 deficiency, 543-547 685-687 331-333 Allgrove syndrome, 331-333 Achalasia, 331-333 Adaptive function, 144-149 Agnosia, 118-122 Amine neurotransmission, S11, Acquired immune deficiency syn- Adenosine deaminase polymor- Agyria, 763 $13 drome, 268-270 phism, 323-324 AIDS, 268-270 L-amino acid decarboxylase, $13 Index 827 Amino acid metabolism, S4-S8 Cavernvous sinus thrombosis, Cytometry, 518-523 610-613, 617-618, 716-722, Amniotic epithelial cells, 265-266 457 Cytoplasmic inclusions, 123-129 746-748, 787-800, 820-821 Amyloid polyneuropathy, 182 Cellulitis, 458 Epileptic aphasia, 696-700 Amyotrophic lateral sclerosis, Central nervous system, 628-635 Dandy-Walker syndrome, Epileptic negative myoclonus, 173-175, 186 Central pontine myelinolysis, 561-562, 660-665 395-399 Amyotrophy, 48, 182 428-432 Dejerine-Sottas disease, 46 Epileptiform disorders, 323 Antiglutamates, 173-174 Centronuclear myopathy, 30 Dementia, 181 Ethosuximide, 395-399 Antipsychotics, 324 Cerebellar system, 554-563, Demyelinating disease, 183, 459, Event-related potentials, 321 Aphasia, 118-122, 696-700 570-582 478 Evoked potentials, 702-707, Apnea, 614-615 Cerebral activation, 209-210 Depacon, 239-242 732-734 Apraxia, 621-627 Cerebral cortex, 98-106 Dermatology, 402, 405 Executive function, 801-805 Arima syndrome, 661 Cerebral glucose metabolism, Dermatomyositis, 184 Exercise, $30 Aromatic L-amino acid decar- 543-547 Developmental disorders, Exertional myalgia, 184 boxylase, S13 Cerebral hemispheres, 655-656 299-302, 322, 660-665, Extensor toe sign, 337-340 Arrhythmia, 229-232, 745-746 Cerebral injury, 683-684 724-727, 787-793 Extraocular muscular disorders, Arteriovenous malformation, Cerebral lesions, 243-248 Developmental right-hemisphere 34-36 685-687 Cerebral neurocytoma, 462 syndrome, 299-302 Extrapontine myelinolysis, Asperger's syndrome, 215, 216 Cerebral palsy, 151-154, 216, Dextromethorphan, 461-462 428-432 Ataxia, 180-181, 554-569, 583-591 289-293 Diabetic radiculoplexopathy, 183 Eye movements, 554-569, 660-665 Atelectasis, 140-142 Cerebral vasculitis, 815-817 Diazepam, 602-608 Atrophy, 43, 139-143, 175-176, Cerebrospinal fluid, 329-331, DiGeorge-velocardiofacial syn- Facial Recognition Test, 243-248 691-694 464—467, S9-S14, 728-731 drome, 754-756 Factor V gene, 749-750 Attention-deficit hyperactivity Ceroid lipofuscinoses, 259-261 Dihydrorhodamine-123, 518-523 Famial brachial plexus neuropa- disorder, 187, 192, 212-213, Cesarean section, 460 Discordant phenotypes, 649-654 thy, 48 299-302, 343-350, 801-805 Charcot-Marie-Tooth neuropathy, Disseminated encephalomyelitis, Familial amyloid polyneuropathy, Auditory brainstem response, 44-49 198-201 182 422-427 Chiari malformations, 229-232, Distal acquired demyelinating Familial neonatal convulsions, Auditory hallucinations, 479-480 446-450, 463 symmetric neuropathy, 183 59-60 Autism, 187, 193, 203-204, 215, Child Behavior Checklist, 299-302 DNA, 479, 610-613 Family Assessment Device, 320-324, 388-393, 462-463, Child Development Inventory, Dodge, Philip R., 537-540 642-647 547-549, 636-640 642-647 Down syndrome, 217 Family functioning, 642-647 Autism Diagnostic Interview- Chorea, 509-513, 815-817 Duane syndrome, 35 Fatty acid, S4—S8 Revised, 636-640 Chromosome 18p, 75-77 Duchenne muscular dystrophy, FDG-PET, 208, 211, 215 Autism Diagnostic Observation Chronic inflammatory polyneu- 139-143 Febrile seizures, 61 Schedule-Generic, 636-640 ropathy, 55-57, 478 Dysembryoplastic neuroepithelial Fetus, 265-266 Autoimmune disorders, 41-43, Cleft, of pons, 461 tumors, 673-677 Fiber-type disproportion, 83-86 268-270, 388-393 COACH syndrome, 662 Dyslexia, 187, 193 Fibromuscular dysplasia, 233-237 Automated tandem mass spec- Cognitive function, 592-596 Dysphasia, 323 Fibrosis syndromes, 35 trometry, S4-S8 Computed tomography, 401-402, Dysplasia, 233-237, 759-768 Flow cytometry, 518-523 Autonomic neuropathy, 185-186 403, 405 Dystonia, 75-77 Fluorodeoxyglucose, 673-677 Autosomal-recessive disorder, Congenital extraocular muscular Dystrophin, 27 Focal cortical dysplasia, 765-766 660-665 disorders, 34-36 Dystrophinopathy, 28 Focal epileptogenic electroen- Axonal polyneuropathy, 459-460 Congenital fiber-type dispropor- Dystrophy, 26-34, 139-143, 181, cephalographic patterns, tion myopathy, 83-86 363-366, 462, 471-472, 108-112 Baclofen, 75-77, 408-409 Congenital heart defects, 702-707 543-547, 711-715 Folinic acid, 529-532 Barbiturates, 597-600 Congenital human immunodefi- 4.1 Tesla spectrometer, 524-528 Beck Depression Inventory, ciency virus infection, 268-270 ECG, 402, 404, 405 Fragile-X syndrome, 108-112 642-647 Congenital hydranencephalic- Echocardiography, 402, 404, 405 Free radicals, 382-386 Behavior, 88-95, 144-149 hydrocephalic syndrome, EEG, 88-95, 108-112, 343-350, Frontal lobe epilepsy, 60-61 162-167, 299-302, 592-596 131-134, 824 402, 403, 459, 533-535, Fukuyama muscular dystrophy, Benign familial neonatal convul- Congenital hydrocephalus, 762-763, 781-785, 795-800 711-715 sions, 59-60 144-149 Electrocardiography, 402, 404, Functional brain imaging, 207-218 Benign macrocephaly, 678-682 Congenital intramedullary tumor, 405 Functional magnetic resonance Benzodiazepines, 597-600 467-469 Electrodiagnosis, 156-158, imaging, 210, 304-314 Berg, Bruce O., 736-744 Congenital muscular dystrophy, 692-693 Bilateral cortical dysplasia, 764 27, 28-30, 181 Electroencephalogram, 88-95, GABA, S9-S14 Biochemistry, $31-S32 Congenital myasthenic syn- 108-112, 343-350, 402, 403, Gastroesophageal reflux, 461 Biogenic amine neurotransmis- dromes, 38-41 459, 533-535, 762-763, Gender, 98-106 sion, $11, $13 Congenital myopathies, 30-31, 781-785, 795-800 Generalized convulsive status Bone marrow transplantation, 83-86, 186 Electrographic status epilepticus, epilepticus, 597-608 222-227 Congenital myotonic dystrophy, 334-336 Generalized seizures, 61, 459, 486, Botulinum toxin, 781-785 471472 Electromyography, 180, 781-785 597-608 Botulism, 156-158 Convulsions, 59-60, 486, 487 Electron microscopy, $31 Genetic metabolic Brain, 15-24, 88-95, 125-126, Convulsive status epilepticus, Emery-Dreifuss muscular dystro- encephalopathies, S9-S14 207-218, 320, 331-333, 458, 597-608 phy, 27 Genetics, 159-160, 187-194, 271, 460, 474, 668 Coping, 642-647 EMG, 180, 781-785 403, 405, 411-415, 574-582, Brain stem, 229-232, 422-427, Corpus callosotomy, 282-287 Encephalitis, 1-9 610-613, 660-665, 668, 570-572, 703-704 Corpus callosum, 458, 754~756 Encephalomyelitis, 198-201 $25-S28, $33, 693, 749, 806-811 Cortex, 98-106 Encephalomyelopathy, 325-329 Glioma, 352-356 Calcium channels, 62-63 Cortical dysplasia, 759-768 Encephalomyopathy, 217, Glomerulonephritis, 185 California encephalitis, 1-9 Cortical reorganization, 458 $23-S34 Glucose metabolism, 543-547 Cancer, 184 Cranial computed tomography, Encephalopathy, 249-255, 277-280, Glutaricaciduria type I, 459-460 Carbamazepine, 357-361, 401-403, 405 486, 487, S1-S3, S9-S14 Glycine, 464467 716-722, 751-753 Cranial magnetic resonance Endocrinopathy, 181-182 Glycobiology, $17-S18 Carbohydrate-deficient glycopro- imaging, 708-710 Entrapment neuropathy, 462 Glycoprotein syndromes, tein syndromes, S16-S21 Cranial nerve schwannoma, 67-68 Enuresis, 541-542 $16-S21 Cardiac system, 83-86, 181, Craniofacial dysmorphisms, 461 Enzymes, 382-386 Gross Motor Function Measure, 229-232, 745-746 Critical illness myopathy, 182-183 Ependyma, 473-476 304-314 Cardiomyopathy, 181 Crush head injuries, 496-500 Epilepsy, 15-24, 58-64, 108-117, Group A xeroderma pigmento- Caregivers, 642-647 CT, 401-403, 405 151-154, 181, 202, 271-272, sum, 168-172 L-Carnitine, 162-167 Cytochrome oxidase, $30 289-293, 322, 323, 341, 357-361, Guillain-Barré syndrome, 55-57, Caveolin-3 deficiency, 33-34 Cytokines, 418-421 395-399, 460, 462, 485-495, 480-481 828 Journal of Child Neurology / Volume 14, Number 12, December 1999 Haemophilus influenzae, 458 Judgment of Line Orientation Mitochondrial dysfunction, Neuronal measures, 98-106 Hallervorden-Spatz syndrome, Test, 243-248 131-134, 824 Neuronal storage disease, 123-129 180 Jugular vein thrombosis, 457 Mitochondrial encephalomyopa- Neuropathology, 655-659 Hallucinations, 479-480 Juvenile autism, 215 thy, 217, S23-S34 Neuropathy, 43-53, 67-68, 183, Hand Apraxia Scale, 162-167 Juvenile metachromatic leukody- Mitochondrial myopathy, 37-38 185-186, 462 Headaches, 451-454, 479-480 strophy, 222-227 Mitochondrial respiratory chain, Neuropsychiatric disorders, Head and neck anomalies, 136 518-523 207-218, 618-619 Head injuries, 496-500 Ketogenic diet, 469-471, 696-700 Molar tooth sign, 368-376, Neuropsychological function, Heart defects, 702-707 Krabbe disease, 457-458 583-591, 660-665 144-149, 357-361 Hemidecortication, 304-414 Molecular genetics, 43-50, 403, Neuroradiology, $30 Hemimegalencephaly, 765-766 La Crosse encephalitis, 1-9 405, 411-415, $33 Neurotransmission, $11, S13 Hemispheric language domi- Lactic acidosis, 217 Monomelic amyotrophy, 182 Neurotrophic factors, 164-175 nance, 78-81 Lafora’s disease, 745-746 Mononucleosis, 732-734 Niaprazine, 547-550 Hereditary ataxia, 180-181 Lambert-Eaton myasthenic syn- Monozygotic twins, 649-654, 669 Nonepileptic myoclonia, 756-758 Hereditary neuralgic amyotrophy, drome, 42 Mood disorders, 213-214 Nonketotic hyperglycinemia, 48 Lamellar cytoplasmic inclusions, Motor function, 304-314, 704-705 461-462, 464-467 Hereditary neuropathies, 43-53 123-129 Motor neuron disease, 173-178 Nonverbal learning disorders, 617 Hereditary neuropediatric dis- Laminar heterotopia, 282-287 Moyamoya disease, 268-270 Nystagmus, 623-625 eases, 457 Lamotrigine, 282-287 M proteins, 181-182 Hereditary sensory autonomic Landau-Kleffner syndrome, MRI, 78-81, 210, 304-314, 352-356, Obsessive-compulsive disorder, neuropathy, 185-186 118-122, 215, 216 401-402, 628-635, 674-675, 214-215 Heteroplasmy, $25 Language, 78-81, 118-122 678-684, 708-710, 760, 763 Occipital electrographic status Heterotopias, 282-287, 331-333, Laser therapy, 541-542 MRS, 211 epilepticus, 334-336 763-765 Lateral sclerosis, 173-175, 186 Mucopolysaccharidosis, 462 Occipitoparietal encephalopathy, Hippocampus, 428-432 Learning disorders, 617, 795-800 Muscle biopsy, S30 277-280 HIV, 268-270 Leber's amaurosis, 621 Muscle contractures, 183-184 Ocular defects, 621-627 HMPAO SPECT, 509-513 Leigh syndrome, 325-329, S27-S28 Muscle-eye-brain disease, 711-715 Oculomotor defects, 621-627 Homeodomain protein, 471-472 Lesions, 181, 229-232, 243-248 Muscular atrophy, 43, 139-143, Ohtahara syndrome, 486 Human immunodeficiency virus Leukodystrophy, 222-227 175-176, 691-694 Ophthalmology, 402, 404 infection, 268-270 Leukoencephalopathy, 277-280, Muscular dystrophy, 26-34, Orbital cellulitis, 458 Hunter’s Hope Krabbe Disease 728-731 139-143, 181, 711-715 Organic acid, S4-S8 Registry, 457-458 Leukomalacia, 377-380 Myalgia, 184 Organomegaly, 181-182 Hydranencephalic-hydrocephalic Limb-girdle muscular dystrophy, Myasthenia gravis, 41-42, 478 Ornithine transcarbamylase defi- syndrome, 131-134, 824 26-27, 31-34 Myasthenic syndromes, 38—41, 42 ciency, 533-535 Hydrocephalus, 144-149, Limb lengthening, 183-184 Myelination, 756-758 329-331, 461 Lipofuscinoses, 259-261 Myelinolysis, 428-432 Palsy, 151-154, 216, 289-293 Hyperglycinemia, 461-462, Lissencephaly, 763 Myelopathy, 459 Panencephalitis, 418-427 464-467 Lumbar puncture, S9-S14 Myoclonia, 756-758 Parasagittal cerebral injury. Hypermetabolism, 509-513 Lung disease, 404 Myoclonic epilepsy, 395-399, 486, 683-684 Hyperpnea, 554-563, 565-569 Lymphocytes, 418-421 487, 610-613, 746-748 Partial seizures, 108-112, Hypertensive encephalopathy, Myoclonus, 395-399, 781-785 357-361, 395-399, 486, 487 277-280 Macrocephaly, 678-682 Myoglobinuria, 184 Patient Well-Being Index, 162-167 Hypocalcemic seizures, 458 Macrogyria, 763 Myopathy, 30-31, 37-38, 83-86, Pentobarbital, 602-608 Hypomelanotic macules, 456-457 Magnetic resonance imaging, 180-183, 186 Perinatal mortality, 440-444 Hypoplasia, 660-665 78-81, 210, 304-314, 352-356, Myotonic dystrophy, 471-472 Periventricular brain heterotopia, Hypotension, 822-823 401-402, 628-635, 674-675, 331-333 Hypotonia, 583-591, 660-665 678-684, 708-710, 760, 763 Necrotizing encephalomyelopa- Periventricular leukomalacia, Magnetic resonance spectroscopy, thy, 325-329 377-380 Ictal electroencephalogram, 459 211, 462463, 524-528 Necrotizing encephalopathy, Peroxisomes, 258-259, 434-438 IgA nephropathy, 185 Magnetic source imaging, 211 249-255 Pervasive development disorder, Image fusion, 210-211 Magnetoencephalography, 211 Nemaline myopathy, 30 322 Immunization, 456 Marin-Amat syndrome, 266—267 Neonatal convulsions, 59-60, 486 PET, 208, 209, 211, 213, 215, Immunoglobulin therapy, Markesbery-Udd distal myopathy, Neonatal seizures, 458, 529-532 321-322, 673-677 203-204, 480-481 180 Neonatal suck reflex, 614-615 Pharmacia PhastSystem, 168-172 Infantile botulism, 156-158 Mass spectrometry, S4-S8 Neonatal tumor, 467-469 Pharmacy prescription misfilling, Infantile neuroaxonal dystrophy, Matching Familiar Figures Test, Neonates, 485-486, S4-S8, 708-710 263-264 543-547 801-805 Nephronophthisis, 662 Phenobarbital, 529-532, 820-821 Infantile spasms, 71-74, 323, 487 Medulla, 656-658 Nephropathy, 185 Phenotypes, 649-654 Infants, 156-158, 485-488, Medulloblastoma, 411-415 Nerve conduction, 180 Phenylketonuria, 216-217 496-507, 514-516, 702-707 MELAS, 217 Nervous system, 271 Phenytoin, 130-131, 529-532 Infectious mononucleosis, Melatonin, 481 Neuralgic amyotrophy, 48 Phosphorus magnetic resonance 732-734 Meningomyelocele, 473-476 Neural tube defects, 159-160 spectroscopy, 211, 462-463 Inferior vermis lobules, 320 Mental retardation, 151-154 Neuroaxonal dystrophy, 462, Plantar response, 514-516 Inflammatory cytokines, 418—421 Mental status, 772-780 543-547 Plasma glycine ratio, 464-467 Inflammatory polyneuropathy, Merosin, 181 Neurocytoma, 462 Pneumonia, 140-142 53-57, 459 Merosinopathy, 28 Neurodegenerative diseases, POEMS syndrome, 181-182 Inherited neurodegenerative dis- Metabolic encephalopathies, 256-261 Polymerase chain reaction, eases, 256-261 $1-S3, S9-S14 Neurodevelopmental disorders, 168-172, S30-S31 Intensive care unit, 139-143 Metabolism, 543-547, S1-S3, 187-194, 215-216, 403-404 Polymorphism, 168-172, 323-324 Intramedullary tumor, 467-469 $4-S8, S9-S14 Neuroepithelial tumors, 673-677 Polyneuropathy, 53—57, 181-182, Intrauterine growth retardation, Metachromatic leukodystrophy, Neurofibromatosis, 67-68, 352-356 459-460, 478 724-727 222-227 Neurogenetics, 574-582 Polyplasmy, S25 Intravenous immunoglobulin, L-Methionine, 673-677 Neuroimaging, 207-208, 272, 667 Pons, 461, 656 203-204 Methylenetetrahydrofolate reduc- Neuromet, 457 Positron emission tomography, Intravenous valproate, 822-823 tase gene, 159-160, 749-750 Neurometabolic disorders, 457 208, 209, 211, 213, 215, Ion channels, 58-64 Mice, 61-64 Neuromuscular blockers, 182-183 321-322, 673-677 Ischemic stroke, 451-454 Midazolam, 597-600, 602-608 Neuromuscular diseases, 26-50, Posterior fossa malformations, Isoflurane, 602-608 Midbrain, 656 137, 139-143 113-117 Migraines, 451-454, 479-480 Neuromuscular junction, 41-43 Posterior leukoencephalopathy, Joubert syndrome, 368-376, Miller-Fisher syndrome, 184-185 Neuronal ceroid lipofuscinoses, 277-280 553-596, 621-672 Mitochondrial DNA, 479, 610-613 259-261 Postictal psychosis, 818-819 Index 829 Postneonatal deaths, 440-444 Right-hemisphere syndrome, Spectroscopy, 211, 462-463, Transforming growth factor-81, Postpolio syndrome, 176 299-302 524-528 377-380 Potassium channels, 59-60 RNA, 610-613 Spina bifida occulta, 541-542 Tuberous sclerosis, 71-74, 217, Pregnancy loss, 440-444 Rolandic epilepsy, 716-722 Spinal cord, 473-476, 685-687 321, 401-406, 456-457 Prelysosomal disorders, $16-S21 Spinal muscular atrophy, 43, Tumors, 15-24, 271, 411-415, 458, Premature infants, 502-507 Sarcoglycanopathies, 28 139-143, 175-176, 185, 691-694 467-469, 673-677 Prescription misfilling, 263-264 Sarcoglycans, 27 SSCP, 168-172 Twins, 649-654, 669 Proteins, 181-182, 186, 471-472 Saudi children, stroke in, 295-297 Static encephalopathies, 487 Tyrosine hydroxylase deficiency, Pseudocyst, 329-331 Scavenging enzymes, 382-386 Status epilepticus, 239-242, 334-336, $12-S13 Psychiatry, 341 Schizencephaly, 764-765 597-608, 787-793, 822-823 Psychomotor regression, 610-613 Schizophrenia, 216 Status nonepileptic myoclonia, Ultrasonography, 402, 404, 405 Psychosis, 818-819 School-Years Screening Test for 756-758 P300 studies, 88-95 Evaluation of Mental Status, Stimulants, 343 Vagal nerve, 460 Pulmonary monitoring, 186, 404 772-780 Strabismus, 35 Vaginal birth, 460 Pyridoxine, 687-690 Schwannoma, 67-68 Striatal hypermetabolism, Valproate, 490-495, 751-753, Schwartz-Jampel syndrome, 181 509-513 822-823 Quality of Upper Extremity Skills Sclerosing panencephalitis, Stroke, 233-237, 295-297, 451-454 Valproic acid, 239-242 Test, 304-314 418-427 Stroke-like episodes, 217 Vanishing white matter, 728-731 Sclerosis, 71-74, 173-175, 186, Stroop Color-Word Test, 801-805 Vascular steal, 685-687 Rabe, Edward F., 620 217, 321, 401-406, 456-457 Sturge-Weber syndrome, 82, Vasculitic neuropathy, 185 Radiculoplexopathy, 183 Seizures, 61-62, 108-112, 202, 282- 482-483 Vasculitis, 815-817 Radiopharmaceuticals, 209 287, 357-361, 395-399, 446-450, Subacute necrotizing Vein of Galen, 196-197 Reflex myoclonic epilepsy, 487 458, 459, 461, 462, 485-488, 529- encephalomyelopathy, 325-329 Ventilation, 186 Reflex sympathetic dystrophy, 532, 597-608, 687-690, 746-748 Subacute sclerosing panen- Vermian hypoplasia, 661-662 363-366 Senior-Loken syndrome, 661 cephalitis, 418-427 Vigabatrin, 71-74 Refractory epilepsy, 460 Sensory autonomic neuropathy, Subcortical heterotopia, 282-287, Vineland Adaptive Behavioral Refractory generalized convulsive 185-186 763-765 Scale, 144-149 status epilepticus, 597-608 Serotonin transporter, 321-322, Suck reflex, 614-615 Visual evoked potentials, Renal ultrasonography, 402, 404, 324 Sudomotor function, 456-457 732-734 405 Shunted congenital hydro- Sydenham’s chorea, 509-513, Respiratory chain, 518-523, cephalus, 144-149 815-817 Walker-Warburg syndrome, $23-S34 Signoret’s Memory Battery, Symmetric neuropathy, 183 711-715 Respiratory failure, 139-143, 144-149 Syncope, 137 Wechsler Performance IQ, 660-665 Single photon emission com- Systemic cancer, 184 144-149 Respiratory sinus arrhythmia, puted tomography, 208-212, SYSTEMS, 772-780 Weight gain, 490-495 229-232 217-218, 509-513 West syndrome, 485-488 Restriction fragment length poly- Single strand conformation poly- Tandem mass spectrometry, S4-S8 White matter, 181, 728-731 morphism, 168-172 morphism, 168-172 Tesla spectrometer, 524-528 Wilson's disease, 217 Retardation, 151-154, 554-563, Sinus arrhythmia, 229-232 Tetrahydrobiopterin metabolism, Wisconsin Card Sorting Test, 565-569 Sinus thrombosis, 457 $12 801-805 Retinopathy, 661-662 677C +T mutation, 159-160 Thiopental, 602-608 Wnt gene, 660-665 Rett syndrome, 162-167, 215, 216, Skin, 181-182 Thrombocytopenia, 130-131 440-444, 524-528, 550-552, Sleep, 481, 482 Thrombosis, 457 X chromosome, 806-811 806-811 Slow-wave epilepsy, 63-64 Tics, 316-319 Xeroderma pigmentosum, Rett Syndrome Motor Behavioral Sodium benzoate, 461-462 Tourette syndrome, 187, 192, 215, 168-172 Assessment, 162-167 Sodium channels, 61 316-319 X-linked hereditary ataxia, Reversible occipitoparietal Sodium valproate, 751-753 Tower of London Test, 801-805 180-181 encephalopathy, 277-280 Somatosensory evoked poten- Trail Making Test, 801-805 X-linked spinal muscular atrophy, Reversible posterior leukoen- tials, 703 Transcarbamylase deficiency, 185 cephalopathy, 277-280 Spasms, 71-74, 323 533-535 RFLP, 168-172 SPECT, 208-212, 217-218, 509-513 Transfer ribonucleic acid**” gene, Yale Global Tic Severity Scale, Rhombic lip, 574-582 Spectrometry, 524-528, S4-S8 610-613 316-319 Child Neurologist Please take a moment to consider an exciting Child Neurology opportunity that is now available with one of the nation’s largest freestanding children’s hospitals. Live in a beautiful, affordable area of California with easy access to the Sierra Mountains, Yosemite National Park and the Pacific Coast. This brand new 220-bed, state-of-the-art facility services a population of approximately 1 million children. Practice with another Child Neurologist and a team of physicians dedicated to pediatric care. Sub-specialties include neurosurgery, cardiology, orthopedics, trauma and many more. Highly competitive compensation package including malpractice coverage, excellent retirement, healthcare and annual leave benefits. Academic affiliation available. For more information please call, Clint Scott, MDA, 1-800-932-1023 ext.247, fax C.V. to 972-481-1333 or e-mail to [email protected].

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Journal of Child Neurology 1999: Vol 14 Index PDF

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Preview Journal of Child Neurology 1999: Vol 14 Index

Volume 14, 1999 Index Author Index Abe, T, 249, 687 Camfield, P, 617 Elpeleg, ON, 479 Houri, S, 479 Adesina, AM, 411 Campistol, J, 683 El-Schahawi, M, 610 Hove, MT, 621 Akalin, T, 745 Campos, Y, 131 Elwan, MA, 265 Hsiung, G-YR, 268 Akar, E, 749 Capovilla, G, 395, 446 Engel, AG, 38 Hsu, HW, 473 Akar, N, 749 Carollo, C, 352 Engle, E, 34 Huseyinov, A, 418 Albright, AL, 408 Carratala, F, 683 Erzen, C, 678 Hwang, P, 304 Aldenkamp, AP, 795 Carroll, A, 801 Espeel, M, 434 Hyland, K, 529, S9 Alder, J, 574 Carter, LP, 67 Eviatar, L, 490 Alehan, FK, 130 Caruso, JM, 428 Ewing-Cobbs, L, 496 Ibarra, R, 88 Alikasifoglu, M, 159 Castro-Gago, M, 131, 824 Iglesias-Diz, M, 824 Alonso, A, 131 Catsman-Berrevoets, CE, 243 Falcini, F, 363 Imai, K, 756 Alper, G, 678 Cavalier, L, 660 Farmer, PM, 123 Inagaki, M, 422 Alshansky, A, 490 Chabot, RJ, 343 Fattal-Valevski, A, 724 Incorpora, G, 196 Al-Sulaiman, A, 295 Chace, DH, $4 Feldman-Winter, L, 479 Inui, K, 756 Amat, L, 434 Chalmers, A, 478 Fennell, E, 368, 592, 642 Ishikawa, Y, 168 Anar, B, 159 Chance, PF, 43, 660 Fernandez Alvarez, E, 683 Ismail, H, 295 Andermann, E, 565 Chee, CM, 696 Ferri, R, 446 Andermann, F, 554, 565 Chez, MG, 239 Fiumara, A, 550 Jackson, AH, 464 Anderson, A, 502 Chiarelli, F, 746 Flitman, HP, 473 Jaeken, J, 728 Anlar, B, 198 Chiba, S, 471 Fontaine, S, 565 Jaffa, A, 724 Antony, JH, 815 Chiodo, S, 113 Frank, Y, 277 Janisch, C, 467 Apak, RA, 198 Christodoulou, J, 162, 518 Freeman, JM, 469 Jay, V, 83 Applegarth, DA, 464 Chudnow, R, 272 Frye, VH, 388 Jaynes, M, 325, 341, 481 Aracil, A, 434 Chun, RWM, 1 Fujii, T, 265 Joubert, M, 554, 565 Arenas, J, 131 Chusid, R, 277 Fukuyama, Y, 26 Arends, J, 795 Cimaz, R, 363 Fyfe, S, 440 Kaga, M, 118, 422 Arikan, ©, 678 Clementi, M, 352 Kalra, V, 541 Arnold, LA, S9 Coakley, JC, 518 Gabreéls, F, 37, 728 Kanakoudi, FG, 480 Arpino, C, 151 Comair, YG, 15 Gabreéls-Festin, A, 52 Kandt, RS, 401 Auerbach, JG, 299 Comi, AM, 388 Gale, S, 636 Kapaun, P, 222 Autret, A, 144 Conill, J, 434 Garozzo, R, 266 Kaplan, AM, 673 Awaad, Y, 75, 316, 781 Corcia, P, 144 Gartside, PS, 602 Katzos, GS, 480 Coutinho, LMB, 467 Gascon, GG, 207 Kawashima, K, 265 Bademosi, 0, 295 Coyne, MF, 781 Gawehn, J, 451 Khajavi, K, 15 Bagan, BT, 239 Crawford, G, 343 Gay, CT, 341 Ko, TS, 282 Bandy, DJ, 673 Crawley, A, 304 Geng, S, 745 Koenig, M, 660 Bandyopadhyay, S, 685 Creten, WL, 243 Gerez, M, 88 Kohlschiietter, A, 222 Banwell, BL, 83 Curatolo, P, 136, 151, 446, 618 Ghosh, D, 337, 339 Kontopoulos, EE, 289, 480, 514 Barkovich, AJ, 628 Gilbert, DL, 469, 597, 602 Kornreich, L, 331 Barnard, C, 787 D’Agata, M, 547 Gillet, P, 144 Kose, G, 198 Barone, R, 550 Darras, BT, 620 Gingold, MK, 325, 481, 482 Kramer, U, 485 Barr, J, 732 D’Asero, G, 550 Giros, M, 434 Kraynack, NC, 754 Barthez, MA, 144 Dean, DE, 98 Gitten, J, 368, 592, 642 Kremenopoulos, GM, 514 Barzilai, A, 732 de Courten-Myers, GM, 98, 473 Glauser, TA, 382, 597, 602 Kunkel, L, 33 Battistella, A, 352 Deda, G, 749 Goebel, HH, 30 Kuppusamy, K, 78 Bauer, L, 229 Dede, D, 368, 592, 642 Goldberg, S, 649 Kurahashi, H, 756 Baumgartner, J, 496 de Menezes, MS, 268 Gombakis, NP, 480 Kure, S, 464, 728 Baxter, D, 229 Desnick, RJ, 543 Gordon, RE, 78 Kuroki, S, 711 Beaty, BJ, 1 de Toffol, B, 144 Granitzny, B, 222 Kutai, M, 724 Beccaria, F, 395 De Vivo, DC, $1, $23 Graveline, C, 304 Kutukculer, N, 418 Becker, LE, 83 Devoti, M, 357 Greco, R, 746 Beiras-Igiesias, A, 131 Dickstein, DP, 207 Grond, M, 543 Lahat, E, 732 Berg, BO, 736 Dilenge, M-E, 509 Gross-Tsur, V, 299 Landau, YE, 299 Bergqvist, AGC, 696 DiMario, FJ, 401 Grueneich, R, 78 Landry, S, 502 Berkovitch, M, 732 DiMario, FJ Jr, 229, 533 Gupta, S, 203 Lane, JB, 524 Billard, C, 144 DiMauro, S, 610, S23 Langsford, S, 801 Biondi, R, 446 Dinh, L, 509 Haacke, M, 78 Lanska, DJ, 337 Birnkrant, DJ, 139 Dittmann, RW, 222 Haftel, L, 479 Laverda, AM, 352 Black, FH, 772 Dizdarer, G, 418 Hahn, JF, 15 Law, PA, 388 Bodensteiner, JB, 271, 325, 481 Dobyns, WB, 660 Hamano, K, 711 Lawson, MA, 673 Boduroglu, K, 159 Dodge, PR, 537, 620 Hammer, MS, 239 Leary, M, 751 Boltshauser, E, 583 Domizio, S, 746 Hancock, E, 71 Lee, BCP, 78 Bone, G, 304 Douglas, G, 801 Harel, S, 724 Lee, JK, 282 Bonilla, E, $23 Dubowitz, V, 26 Harris, MJ, 343 Leech, RW, 67, 136, 271 Boénnemann, CG, 31 Duchowny, M, 759 Hatten, ME, 574 Leitner, Y, 724 Bonstelle, CT, 673 Dye, D, 440 Hecox, KE, 156 Leonard, H, 162, 440 Boor, R, 451 Heiss, W-D, 543 Leonard, S, 440 Bornholt, L, 772 Ebinger, F, 451 Hemingway, C, 751 Lerman, P, 820 Britton, BH, 67 Ehlers, JAC, 467 Hendy, J, 772 Lerman-Sagie, T, 331, 479, 818, 820 Brooks-Kayal, AR, 696 Eiben, RM, 139 Herndon, RM, 275 Levy, HL, 464 Brown, WD, 428 Eickhoff, W, 222 Hetherington, H, 524 Lieberman, D, 724 Brumback, A, 202 Eiris-Punal, J, 131, 824 Higgins, G, 162 Limperopoulos, C, 702 Brumback, RA, 67, 482, 617 Eisenring, J-J, 554 Hobbs, GR, 614 Lin, W, 78 Brunquell, P, 533 Ekinci, G, 678 Holden, KR, 708 Loeffel, M, 239 Buist, NMR, 529 Elgamal, A, 781 Hommet, C, 144 Lopez, L, 618 Bujanover, Y, 818 El-Ghazzawy, O, 78 Horikawa, M, 329 Lorberboym, M, 818 Burde, R, 649 Elia, M, 446 Hostoffer, RW, 754 Lotz, BP, 156 Butler, IJ, 137 Ellaway, C, 162 Houghton, S, 801 Lourmiere, JM, 144 826 Journal of Child Neurology / Volume 14, Number 12, December 1999 Luescher, JL, 642 Osborn, JP, 71 Rosenblatt, B, 702 Titanic-Schefft, M, 382 Lutchka, LM, 696 O’Tuama, LA, 207 Rossi, PG, 113, 547 Titus, MO, 708 Ouvrier, R, 53, 772 Rubboli, G, 395 Toda, T, 711 Magboll, G, 295 Overweg-Plandsoen, WCG, 795 Rudolf, J, 543 Tomer, A, 724 Majnemer, A, 702 Ozonoff, S, 636 Ruiz, M, 434 Tominaga, K, 329 Malkin, E, 610 Ozyiirek, R, 745 Russell, EC, 130 Toone, JR, 464 Mallet, A, 88 Rust, RS, 1 Topaloglu, H, 198 Mancias, P, 137 Palaksha, HK, 541 Ryan, MM, 815 Torres, OA, 529 Mandich, M, 614 Palmer, J, 15 Ryan, SG, 58, 187 Tran, TX, 583 Mano, T, 756 Palmer, SC, 583 Trifiletti, RR, 196, 266 Manson, J, 108 Pampols, T, 434 Sabatino, G, 746 Tsikoulas, I, 289, 514 Manwaring, KH, 673 Pan, JW, 534 Sakuragawa, N, 265 Tuncbilek, E, 159 Many, A, 724 Paquier, PF, 243 Santini, JJ, 144 Turanli, G, 198 Marcus, JC, 337 Parano, E, 196, 266 Santos, CS, 822 Tusa, RJ, 621 Maria, BL, 368, 553, 583, 592, 628, 642 Paret, G, 732 Santucci, M, 113 Tutuncuoglu, S, 418 Marzullo, E, 550 Parmeggiani, A, 113, 547 Satran, D, 660 Tiitiitiinciioglu, S, 745 Matthews, CG, 1 Patterson, MC, S16 Scaduto, MC, 113 Matucci-Cerinic, M, 363 Pavia, C, 434 Schanen, NC, 806 Vajsar, J, 83 Maytal, J, 490 Pavlakis, SG, 277 Schindler, D, 543 Van Campen, LE, 67 McAbee, G, 479 Pavone, L, 550 Schlegal, B, 751 van der Knaap, MS, 728 Meletti, S, 395 Pavone, P, 196, 266 Schochet, SS, 325 Van der Meere, J, 299 Melki, J, 43 Peeden, JN, 388 Schreier, HA, 480 Van Dongen, HR, 243 Mendel, RC, 67 Pellegri, A, 151 Seidel, WT, 716 van Mourik, M, 243 Meng, SZ, 377 Pellegrino, JE, 660 Serfontein, G, 343 van Raaij-Selten, B, 728 Mikulis, D, 304 Pellock, JM, 130 Serrano, C, 88 Van Tassel, P, 708 Millen, KJ, 574 Percy, AK, 256, 524 Shalev, RS, 299 Veggiotti, P, 395 Miller, JN, 636 Perilongo, G, 352 Shanske, A, 649 Verhoeven, NM, 728 Miller, RG, 173 Petetot, JM-C, 98 Shanske, S, 610 Verrotti, A, 746 Miller, VS, 529 Pineda, M, 434 Shelton, F de NAP, 619 Vining, EPG, 469 Millonig, JH, 574 Pintos-Martinez, E, 131 Shenoy, S, 271 Viahov, D, 151 Mimouni, M, 331 Pipitone, E, 547 Sheth, RD, 156, 334, 614, 685 Vossler, DG, 282 Minami, R, 168 Pippenger, CE, 382 Shevell, M, 509, 702 Mitchell, WG, 716 Platania, N, 196 Shikolka, C, 304 Waclawik, AJ, 156 Mitra, N, 123 Plioplys, AV, 203 Shtilbans, A, 610 Wade, S, 304 Moldavsky, M, 818 Poo, P, 683 Shultz, BL, 408 Walker, K, 751 Moras, P, 352 Pope, JF, 139 Shuper, A, 331 Wall, M, 801 Morgese, G, 746 Posar, A, 113, 547 Siddique, Q, 490 Wanders, RJA, 434 Morris, HH, 15 Powell, L, 801 Singh, R, 108 Watanabe, T, 249 Moser, A, 434 Pradhan, S, 337, 339 Sipahi, T, 749 West, J, 801 Moser, HW, 434 Prasad, MR, 496 Smith, K, 502 Wevers, RA, 728 Moss, SD, 673 Ptito, A, 565 Sofia, V, 446 White, JR, 822 Munoz, S, 75 Pullarkat, RK, 123 Spataro, J, 673 Whiting, K, 801 Murgia, A, 352 Puri, V, 233 Spinella, GM, 667 Whiting, S, 759 Musumeci, O, 610 Pyzik, PL, 469 Stanek, J, 473 Wilcken, B, 162 Musumeci, SA, 446 Stazi, MA, 151 Wildin, S, 502 Quisling, RG, 368, 628 Strober, JB, 691 Williams, AJ, 518 Naitoh, H, 422 Stronks, DL, 243 Williams, BJ, 636 Naylor, EW, S4 Rabinowicz, T, 98 Sugai, K, 422 Williams, K, 162 Neeper, R, 207 Rachmel, A, 331 Sumitani, S, 168 Wilson, DA, 67 Neumaier-Probst, E, 222 Rapin, I, 649 Sutherland, GR, 108 Wingate, RJT, 574 Newsom-Davis, J, 41 Raucher, A, 818 Swank, P, 502 Wirrell, E, 787 Nigro, M, 75 Raynes, HR, 649 Sy-Kho, R, 490 Wisniewski, KE, 123 Nihei, K, 422 Reiman, EM, 673 Wulbrand, H, 222 Nissenkorn, A, 818 Reitter, B, 451 Tachi, N, 471 Wyllie, E, 15 Northrup, H, 401 Richards, SD, 614 Takashima, S, 377 Novak, GP, 490 Riggs, G, 233 Takayama, S, 422 Yachnis, AT, 368, 570, 655 Novo-Rodriguez, MI, 131 Riggs, JE, 334 Tal-Posener, E, 724 Yamada, T, 329 Nowinski, C, 239 Riordan, G, 751 Tam, DA, 478 Yilmaz, Y, 678 Nunes, ML, 467 Ritchie, S, 614 Tassinari, CA, 395 Yoshida, S, 329 Riva, D, 357 Tayem, H, 781 Yoshikawa, H, 249, 687 Oda, Y, 249, 687 Roach, ES, 401 Taylor, GP, 83 Yoshioka, M, 711 Ohya, K, 471 Robb, JP, 554 Tchervenkov, C, 702 Okada, S, 756 Robin, NH, 754 Tekgiil, H, 418, 745 Zafeiriou, DI, 289, 480, 515 Okinaga, T, 756 Roels, F, 434 Tello, A, 88 Zander, A, 222 Oksel, F, 745 Rohlicek, C, 702 Tennekoon, GI, 691 Zeharia, A, 331 Ono, J, 756 Rorke, LB, 570, 655 Teylar, G, 678 Ziegler, DK, 482 Orgill, AA, 343 Rosainz, LC, 368 Tezcan, K, 533 Zimmerman, AW, 388 Orsal, A, 749 Rose, AL, 123 Thompson, WH, 1 Zulian, F, 363 Subject Index Abdominal cerebrospinal fluid Acute inflammatory polyneuropa- Adhalin, 27 Alacrima, 331-333 pseudocyst, 329-331 thy, 53-55 ADHD, 187, 192, 212-213, Alexander's disease, 275-276, Absence seizures, 61-62, 746-748 Acute necrotizing encephalopa- 299-302, 343-350, 801-805 325-329 Acetylcholine, 38-41 thy, 249-255 Adolescents, 144-149, 341 “Alice in Wonderland” syndrome, a-N-Acetylgalactosaminidase Acute spinal cord infarction, Adrenocortical insufficiency, 732-734 deficiency, 543-547 685-687 331-333 Allgrove syndrome, 331-333 Achalasia, 331-333 Adaptive function, 144-149 Agnosia, 118-122 Amine neurotransmission, S11, Acquired immune deficiency syn- Adenosine deaminase polymor- Agyria, 763 $13 drome, 268-270 phism, 323-324 AIDS, 268-270 L-amino acid decarboxylase, $13 Index 827 Amino acid metabolism, S4-S8 Cavernvous sinus thrombosis, Cytometry, 518-523 610-613, 617-618, 716-722, Amniotic epithelial cells, 265-266 457 Cytoplasmic inclusions, 123-129 746-748, 787-800, 820-821 Amyloid polyneuropathy, 182 Cellulitis, 458 Epileptic aphasia, 696-700 Amyotrophic lateral sclerosis, Central nervous system, 628-635 Dandy-Walker syndrome, Epileptic negative myoclonus, 173-175, 186 Central pontine myelinolysis, 561-562, 660-665 395-399 Amyotrophy, 48, 182 428-432 Dejerine-Sottas disease, 46 Epileptiform disorders, 323 Antiglutamates, 173-174 Centronuclear myopathy, 30 Dementia, 181 Ethosuximide, 395-399 Antipsychotics, 324 Cerebellar system, 554-563, Demyelinating disease, 183, 459, Event-related potentials, 321 Aphasia, 118-122, 696-700 570-582 478 Evoked potentials, 702-707, Apnea, 614-615 Cerebral activation, 209-210 Depacon, 239-242 732-734 Apraxia, 621-627 Cerebral cortex, 98-106 Dermatology, 402, 405 Executive function, 801-805 Arima syndrome, 661 Cerebral glucose metabolism, Dermatomyositis, 184 Exercise, $30 Aromatic L-amino acid decar- 543-547 Developmental disorders, Exertional myalgia, 184 boxylase, S13 Cerebral hemispheres, 655-656 299-302, 322, 660-665, Extensor toe sign, 337-340 Arrhythmia, 229-232, 745-746 Cerebral injury, 683-684 724-727, 787-793 Extraocular muscular disorders, Arteriovenous malformation, Cerebral lesions, 243-248 Developmental right-hemisphere 34-36 685-687 Cerebral neurocytoma, 462 syndrome, 299-302 Extrapontine myelinolysis, Asperger's syndrome, 215, 216 Cerebral palsy, 151-154, 216, Dextromethorphan, 461-462 428-432 Ataxia, 180-181, 554-569, 583-591 289-293 Diabetic radiculoplexopathy, 183 Eye movements, 554-569, 660-665 Atelectasis, 140-142 Cerebral vasculitis, 815-817 Diazepam, 602-608 Atrophy, 43, 139-143, 175-176, Cerebrospinal fluid, 329-331, DiGeorge-velocardiofacial syn- Facial Recognition Test, 243-248 691-694 464—467, S9-S14, 728-731 drome, 754-756 Factor V gene, 749-750 Attention-deficit hyperactivity Ceroid lipofuscinoses, 259-261 Dihydrorhodamine-123, 518-523 Famial brachial plexus neuropa- disorder, 187, 192, 212-213, Cesarean section, 460 Discordant phenotypes, 649-654 thy, 48 299-302, 343-350, 801-805 Charcot-Marie-Tooth neuropathy, Disseminated encephalomyelitis, Familial amyloid polyneuropathy, Auditory brainstem response, 44-49 198-201 182 422-427 Chiari malformations, 229-232, Distal acquired demyelinating Familial neonatal convulsions, Auditory hallucinations, 479-480 446-450, 463 symmetric neuropathy, 183 59-60 Autism, 187, 193, 203-204, 215, Child Behavior Checklist, 299-302 DNA, 479, 610-613 Family Assessment Device, 320-324, 388-393, 462-463, Child Development Inventory, Dodge, Philip R., 537-540 642-647 547-549, 636-640 642-647 Down syndrome, 217 Family functioning, 642-647 Autism Diagnostic Interview- Chorea, 509-513, 815-817 Duane syndrome, 35 Fatty acid, S4—S8 Revised, 636-640 Chromosome 18p, 75-77 Duchenne muscular dystrophy, FDG-PET, 208, 211, 215 Autism Diagnostic Observation Chronic inflammatory polyneu- 139-143 Febrile seizures, 61 Schedule-Generic, 636-640 ropathy, 55-57, 478 Dysembryoplastic neuroepithelial Fetus, 265-266 Autoimmune disorders, 41-43, Cleft, of pons, 461 tumors, 673-677 Fiber-type disproportion, 83-86 268-270, 388-393 COACH syndrome, 662 Dyslexia, 187, 193 Fibromuscular dysplasia, 233-237 Automated tandem mass spec- Cognitive function, 592-596 Dysphasia, 323 Fibrosis syndromes, 35 trometry, S4-S8 Computed tomography, 401-402, Dysplasia, 233-237, 759-768 Flow cytometry, 518-523 Autonomic neuropathy, 185-186 403, 405 Dystonia, 75-77 Fluorodeoxyglucose, 673-677 Autosomal-recessive disorder, Congenital extraocular muscular Dystrophin, 27 Focal cortical dysplasia, 765-766 660-665 disorders, 34-36 Dystrophinopathy, 28 Focal epileptogenic electroen- Axonal polyneuropathy, 459-460 Congenital fiber-type dispropor- Dystrophy, 26-34, 139-143, 181, cephalographic patterns, tion myopathy, 83-86 363-366, 462, 471-472, 108-112 Baclofen, 75-77, 408-409 Congenital heart defects, 702-707 543-547, 711-715 Folinic acid, 529-532 Barbiturates, 597-600 Congenital human immunodefi- 4.1 Tesla spectrometer, 524-528 Beck Depression Inventory, ciency virus infection, 268-270 ECG, 402, 404, 405 Fragile-X syndrome, 108-112 642-647 Congenital hydranencephalic- Echocardiography, 402, 404, 405 Free radicals, 382-386 Behavior, 88-95, 144-149 hydrocephalic syndrome, EEG, 88-95, 108-112, 343-350, Frontal lobe epilepsy, 60-61 162-167, 299-302, 592-596 131-134, 824 402, 403, 459, 533-535, Fukuyama muscular dystrophy, Benign familial neonatal convul- Congenital hydrocephalus, 762-763, 781-785, 795-800 711-715 sions, 59-60 144-149 Electrocardiography, 402, 404, Functional brain imaging, 207-218 Benign macrocephaly, 678-682 Congenital intramedullary tumor, 405 Functional magnetic resonance Benzodiazepines, 597-600 467-469 Electrodiagnosis, 156-158, imaging, 210, 304-314 Berg, Bruce O., 736-744 Congenital muscular dystrophy, 692-693 Bilateral cortical dysplasia, 764 27, 28-30, 181 Electroencephalogram, 88-95, GABA, S9-S14 Biochemistry, $31-S32 Congenital myasthenic syn- 108-112, 343-350, 402, 403, Gastroesophageal reflux, 461 Biogenic amine neurotransmis- dromes, 38-41 459, 533-535, 762-763, Gender, 98-106 sion, $11, $13 Congenital myopathies, 30-31, 781-785, 795-800 Generalized convulsive status Bone marrow transplantation, 83-86, 186 Electrographic status epilepticus, epilepticus, 597-608 222-227 Congenital myotonic dystrophy, 334-336 Generalized seizures, 61, 459, 486, Botulinum toxin, 781-785 471472 Electromyography, 180, 781-785 597-608 Botulism, 156-158 Convulsions, 59-60, 486, 487 Electron microscopy, $31 Genetic metabolic Brain, 15-24, 88-95, 125-126, Convulsive status epilepticus, Emery-Dreifuss muscular dystro- encephalopathies, S9-S14 207-218, 320, 331-333, 458, 597-608 phy, 27 Genetics, 159-160, 187-194, 271, 460, 474, 668 Coping, 642-647 EMG, 180, 781-785 403, 405, 411-415, 574-582, Brain stem, 229-232, 422-427, Corpus callosotomy, 282-287 Encephalitis, 1-9 610-613, 660-665, 668, 570-572, 703-704 Corpus callosum, 458, 754~756 Encephalomyelitis, 198-201 $25-S28, $33, 693, 749, 806-811 Cortex, 98-106 Encephalomyelopathy, 325-329 Glioma, 352-356 Calcium channels, 62-63 Cortical dysplasia, 759-768 Encephalomyopathy, 217, Glomerulonephritis, 185 California encephalitis, 1-9 Cortical reorganization, 458 $23-S34 Glucose metabolism, 543-547 Cancer, 184 Cranial computed tomography, Encephalopathy, 249-255, 277-280, Glutaricaciduria type I, 459-460 Carbamazepine, 357-361, 401-403, 405 486, 487, S1-S3, S9-S14 Glycine, 464467 716-722, 751-753 Cranial magnetic resonance Endocrinopathy, 181-182 Glycobiology, $17-S18 Carbohydrate-deficient glycopro- imaging, 708-710 Entrapment neuropathy, 462 Glycoprotein syndromes, tein syndromes, S16-S21 Cranial nerve schwannoma, 67-68 Enuresis, 541-542 $16-S21 Cardiac system, 83-86, 181, Craniofacial dysmorphisms, 461 Enzymes, 382-386 Gross Motor Function Measure, 229-232, 745-746 Critical illness myopathy, 182-183 Ependyma, 473-476 304-314 Cardiomyopathy, 181 Crush head injuries, 496-500 Epilepsy, 15-24, 58-64, 108-117, Group A xeroderma pigmento- Caregivers, 642-647 CT, 401-403, 405 151-154, 181, 202, 271-272, sum, 168-172 L-Carnitine, 162-167 Cytochrome oxidase, $30 289-293, 322, 323, 341, 357-361, Guillain-Barré syndrome, 55-57, Caveolin-3 deficiency, 33-34 Cytokines, 418-421 395-399, 460, 462, 485-495, 480-481 828 Journal of Child Neurology / Volume 14, Number 12, December 1999 Haemophilus influenzae, 458 Judgment of Line Orientation Mitochondrial dysfunction, Neuronal measures, 98-106 Hallervorden-Spatz syndrome, Test, 243-248 131-134, 824 Neuronal storage disease, 123-129 180 Jugular vein thrombosis, 457 Mitochondrial encephalomyopa- Neuropathology, 655-659 Hallucinations, 479-480 Juvenile autism, 215 thy, 217, S23-S34 Neuropathy, 43-53, 67-68, 183, Hand Apraxia Scale, 162-167 Juvenile metachromatic leukody- Mitochondrial myopathy, 37-38 185-186, 462 Headaches, 451-454, 479-480 strophy, 222-227 Mitochondrial respiratory chain, Neuropsychiatric disorders, Head and neck anomalies, 136 518-523 207-218, 618-619 Head injuries, 496-500 Ketogenic diet, 469-471, 696-700 Molar tooth sign, 368-376, Neuropsychological function, Heart defects, 702-707 Krabbe disease, 457-458 583-591, 660-665 144-149, 357-361 Hemidecortication, 304-414 Molecular genetics, 43-50, 403, Neuroradiology, $30 Hemimegalencephaly, 765-766 La Crosse encephalitis, 1-9 405, 411-415, $33 Neurotransmission, $11, S13 Hemispheric language domi- Lactic acidosis, 217 Monomelic amyotrophy, 182 Neurotrophic factors, 164-175 nance, 78-81 Lafora’s disease, 745-746 Mononucleosis, 732-734 Niaprazine, 547-550 Hereditary ataxia, 180-181 Lambert-Eaton myasthenic syn- Monozygotic twins, 649-654, 669 Nonepileptic myoclonia, 756-758 Hereditary neuralgic amyotrophy, drome, 42 Mood disorders, 213-214 Nonketotic hyperglycinemia, 48 Lamellar cytoplasmic inclusions, Motor function, 304-314, 704-705 461-462, 464-467 Hereditary neuropathies, 43-53 123-129 Motor neuron disease, 173-178 Nonverbal learning disorders, 617 Hereditary neuropediatric dis- Laminar heterotopia, 282-287 Moyamoya disease, 268-270 Nystagmus, 623-625 eases, 457 Lamotrigine, 282-287 M proteins, 181-182 Hereditary sensory autonomic Landau-Kleffner syndrome, MRI, 78-81, 210, 304-314, 352-356, Obsessive-compulsive disorder, neuropathy, 185-186 118-122, 215, 216 401-402, 628-635, 674-675, 214-215 Heteroplasmy, $25 Language, 78-81, 118-122 678-684, 708-710, 760, 763 Occipital electrographic status Heterotopias, 282-287, 331-333, Laser therapy, 541-542 MRS, 211 epilepticus, 334-336 763-765 Lateral sclerosis, 173-175, 186 Mucopolysaccharidosis, 462 Occipitoparietal encephalopathy, Hippocampus, 428-432 Learning disorders, 617, 795-800 Muscle biopsy, S30 277-280 HIV, 268-270 Leber's amaurosis, 621 Muscle contractures, 183-184 Ocular defects, 621-627 HMPAO SPECT, 509-513 Leigh syndrome, 325-329, S27-S28 Muscle-eye-brain disease, 711-715 Oculomotor defects, 621-627 Homeodomain protein, 471-472 Lesions, 181, 229-232, 243-248 Muscular atrophy, 43, 139-143, Ohtahara syndrome, 486 Human immunodeficiency virus Leukodystrophy, 222-227 175-176, 691-694 Ophthalmology, 402, 404 infection, 268-270 Leukoencephalopathy, 277-280, Muscular dystrophy, 26-34, Orbital cellulitis, 458 Hunter’s Hope Krabbe Disease 728-731 139-143, 181, 711-715 Organic acid, S4-S8 Registry, 457-458 Leukomalacia, 377-380 Myalgia, 184 Organomegaly, 181-182 Hydranencephalic-hydrocephalic Limb-girdle muscular dystrophy, Myasthenia gravis, 41-42, 478 Ornithine transcarbamylase defi- syndrome, 131-134, 824 26-27, 31-34 Myasthenic syndromes, 38—41, 42 ciency, 533-535 Hydrocephalus, 144-149, Limb lengthening, 183-184 Myelination, 756-758 329-331, 461 Lipofuscinoses, 259-261 Myelinolysis, 428-432 Palsy, 151-154, 216, 289-293 Hyperglycinemia, 461-462, Lissencephaly, 763 Myelopathy, 459 Panencephalitis, 418-427 464-467 Lumbar puncture, S9-S14 Myoclonia, 756-758 Parasagittal cerebral injury. Hypermetabolism, 509-513 Lung disease, 404 Myoclonic epilepsy, 395-399, 486, 683-684 Hyperpnea, 554-563, 565-569 Lymphocytes, 418-421 487, 610-613, 746-748 Partial seizures, 108-112, Hypertensive encephalopathy, Myoclonus, 395-399, 781-785 357-361, 395-399, 486, 487 277-280 Macrocephaly, 678-682 Myoglobinuria, 184 Patient Well-Being Index, 162-167 Hypocalcemic seizures, 458 Macrogyria, 763 Myopathy, 30-31, 37-38, 83-86, Pentobarbital, 602-608 Hypomelanotic macules, 456-457 Magnetic resonance imaging, 180-183, 186 Perinatal mortality, 440-444 Hypoplasia, 660-665 78-81, 210, 304-314, 352-356, Myotonic dystrophy, 471-472 Periventricular brain heterotopia, Hypotension, 822-823 401-402, 628-635, 674-675, 331-333 Hypotonia, 583-591, 660-665 678-684, 708-710, 760, 763 Necrotizing encephalomyelopa- Periventricular leukomalacia, Magnetic resonance spectroscopy, thy, 325-329 377-380 Ictal electroencephalogram, 459 211, 462463, 524-528 Necrotizing encephalopathy, Peroxisomes, 258-259, 434-438 IgA nephropathy, 185 Magnetic source imaging, 211 249-255 Pervasive development disorder, Image fusion, 210-211 Magnetoencephalography, 211 Nemaline myopathy, 30 322 Immunization, 456 Marin-Amat syndrome, 266—267 Neonatal convulsions, 59-60, 486 PET, 208, 209, 211, 213, 215, Immunoglobulin therapy, Markesbery-Udd distal myopathy, Neonatal seizures, 458, 529-532 321-322, 673-677 203-204, 480-481 180 Neonatal suck reflex, 614-615 Pharmacia PhastSystem, 168-172 Infantile botulism, 156-158 Mass spectrometry, S4-S8 Neonatal tumor, 467-469 Pharmacy prescription misfilling, Infantile neuroaxonal dystrophy, Matching Familiar Figures Test, Neonates, 485-486, S4-S8, 708-710 263-264 543-547 801-805 Nephronophthisis, 662 Phenobarbital, 529-532, 820-821 Infantile spasms, 71-74, 323, 487 Medulla, 656-658 Nephropathy, 185 Phenotypes, 649-654 Infants, 156-158, 485-488, Medulloblastoma, 411-415 Nerve conduction, 180 Phenylketonuria, 216-217 496-507, 514-516, 702-707 MELAS, 217 Nervous system, 271 Phenytoin, 130-131, 529-532 Infectious mononucleosis, Melatonin, 481 Neuralgic amyotrophy, 48 Phosphorus magnetic resonance 732-734 Meningomyelocele, 473-476 Neural tube defects, 159-160 spectroscopy, 211, 462-463 Inferior vermis lobules, 320 Mental retardation, 151-154 Neuroaxonal dystrophy, 462, Plantar response, 514-516 Inflammatory cytokines, 418—421 Mental status, 772-780 543-547 Plasma glycine ratio, 464-467 Inflammatory polyneuropathy, Merosin, 181 Neurocytoma, 462 Pneumonia, 140-142 53-57, 459 Merosinopathy, 28 Neurodegenerative diseases, POEMS syndrome, 181-182 Inherited neurodegenerative dis- Metabolic encephalopathies, 256-261 Polymerase chain reaction, eases, 256-261 $1-S3, S9-S14 Neurodevelopmental disorders, 168-172, S30-S31 Intensive care unit, 139-143 Metabolism, 543-547, S1-S3, 187-194, 215-216, 403-404 Polymorphism, 168-172, 323-324 Intramedullary tumor, 467-469 $4-S8, S9-S14 Neuroepithelial tumors, 673-677 Polyneuropathy, 53—57, 181-182, Intrauterine growth retardation, Metachromatic leukodystrophy, Neurofibromatosis, 67-68, 352-356 459-460, 478 724-727 222-227 Neurogenetics, 574-582 Polyplasmy, S25 Intravenous immunoglobulin, L-Methionine, 673-677 Neuroimaging, 207-208, 272, 667 Pons, 461, 656 203-204 Methylenetetrahydrofolate reduc- Neuromet, 457 Positron emission tomography, Intravenous valproate, 822-823 tase gene, 159-160, 749-750 Neurometabolic disorders, 457 208, 209, 211, 213, 215, Ion channels, 58-64 Mice, 61-64 Neuromuscular blockers, 182-183 321-322, 673-677 Ischemic stroke, 451-454 Midazolam, 597-600, 602-608 Neuromuscular diseases, 26-50, Posterior fossa malformations, Isoflurane, 602-608 Midbrain, 656 137, 139-143 113-117 Migraines, 451-454, 479-480 Neuromuscular junction, 41-43 Posterior leukoencephalopathy, Joubert syndrome, 368-376, Miller-Fisher syndrome, 184-185 Neuronal ceroid lipofuscinoses, 277-280 553-596, 621-672 Mitochondrial DNA, 479, 610-613 259-261 Postictal psychosis, 818-819 Index 829 Postneonatal deaths, 440-444 Right-hemisphere syndrome, Spectroscopy, 211, 462-463, Transforming growth factor-81, Postpolio syndrome, 176 299-302 524-528 377-380 Potassium channels, 59-60 RNA, 610-613 Spina bifida occulta, 541-542 Tuberous sclerosis, 71-74, 217, Pregnancy loss, 440-444 Rolandic epilepsy, 716-722 Spinal cord, 473-476, 685-687 321, 401-406, 456-457 Prelysosomal disorders, $16-S21 Spinal muscular atrophy, 43, Tumors, 15-24, 271, 411-415, 458, Premature infants, 502-507 Sarcoglycanopathies, 28 139-143, 175-176, 185, 691-694 467-469, 673-677 Prescription misfilling, 263-264 Sarcoglycans, 27 SSCP, 168-172 Twins, 649-654, 669 Proteins, 181-182, 186, 471-472 Saudi children, stroke in, 295-297 Static encephalopathies, 487 Tyrosine hydroxylase deficiency, Pseudocyst, 329-331 Scavenging enzymes, 382-386 Status epilepticus, 239-242, 334-336, $12-S13 Psychiatry, 341 Schizencephaly, 764-765 597-608, 787-793, 822-823 Psychomotor regression, 610-613 Schizophrenia, 216 Status nonepileptic myoclonia, Ultrasonography, 402, 404, 405 Psychosis, 818-819 School-Years Screening Test for 756-758 P300 studies, 88-95 Evaluation of Mental Status, Stimulants, 343 Vagal nerve, 460 Pulmonary monitoring, 186, 404 772-780 Strabismus, 35 Vaginal birth, 460 Pyridoxine, 687-690 Schwannoma, 67-68 Striatal hypermetabolism, Valproate, 490-495, 751-753, Schwartz-Jampel syndrome, 181 509-513 822-823 Quality of Upper Extremity Skills Sclerosing panencephalitis, Stroke, 233-237, 295-297, 451-454 Valproic acid, 239-242 Test, 304-314 418-427 Stroke-like episodes, 217 Vanishing white matter, 728-731 Sclerosis, 71-74, 173-175, 186, Stroop Color-Word Test, 801-805 Vascular steal, 685-687 Rabe, Edward F., 620 217, 321, 401-406, 456-457 Sturge-Weber syndrome, 82, Vasculitic neuropathy, 185 Radiculoplexopathy, 183 Seizures, 61-62, 108-112, 202, 282- 482-483 Vasculitis, 815-817 Radiopharmaceuticals, 209 287, 357-361, 395-399, 446-450, Subacute necrotizing Vein of Galen, 196-197 Reflex myoclonic epilepsy, 487 458, 459, 461, 462, 485-488, 529- encephalomyelopathy, 325-329 Ventilation, 186 Reflex sympathetic dystrophy, 532, 597-608, 687-690, 746-748 Subacute sclerosing panen- Vermian hypoplasia, 661-662 363-366 Senior-Loken syndrome, 661 cephalitis, 418-427 Vigabatrin, 71-74 Refractory epilepsy, 460 Sensory autonomic neuropathy, Subcortical heterotopia, 282-287, Vineland Adaptive Behavioral Refractory generalized convulsive 185-186 763-765 Scale, 144-149 status epilepticus, 597-608 Serotonin transporter, 321-322, Suck reflex, 614-615 Visual evoked potentials, Renal ultrasonography, 402, 404, 324 Sudomotor function, 456-457 732-734 405 Shunted congenital hydro- Sydenham’s chorea, 509-513, Respiratory chain, 518-523, cephalus, 144-149 815-817 Walker-Warburg syndrome, $23-S34 Signoret’s Memory Battery, Symmetric neuropathy, 183 711-715 Respiratory failure, 139-143, 144-149 Syncope, 137 Wechsler Performance IQ, 660-665 Single photon emission com- Systemic cancer, 184 144-149 Respiratory sinus arrhythmia, puted tomography, 208-212, SYSTEMS, 772-780 Weight gain, 490-495 229-232 217-218, 509-513 West syndrome, 485-488 Restriction fragment length poly- Single strand conformation poly- Tandem mass spectrometry, S4-S8 White matter, 181, 728-731 morphism, 168-172 morphism, 168-172 Tesla spectrometer, 524-528 Wilson's disease, 217 Retardation, 151-154, 554-563, Sinus arrhythmia, 229-232 Tetrahydrobiopterin metabolism, Wisconsin Card Sorting Test, 565-569 Sinus thrombosis, 457 $12 801-805 Retinopathy, 661-662 677C +T mutation, 159-160 Thiopental, 602-608 Wnt gene, 660-665 Rett syndrome, 162-167, 215, 216, Skin, 181-182 Thrombocytopenia, 130-131 440-444, 524-528, 550-552, Sleep, 481, 482 Thrombosis, 457 X chromosome, 806-811 806-811 Slow-wave epilepsy, 63-64 Tics, 316-319 Xeroderma pigmentosum, Rett Syndrome Motor Behavioral Sodium benzoate, 461-462 Tourette syndrome, 187, 192, 215, 168-172 Assessment, 162-167 Sodium channels, 61 316-319 X-linked hereditary ataxia, Reversible occipitoparietal Sodium valproate, 751-753 Tower of London Test, 801-805 180-181 encephalopathy, 277-280 Somatosensory evoked poten- Trail Making Test, 801-805 X-linked spinal muscular atrophy, Reversible posterior leukoen- tials, 703 Transcarbamylase deficiency, 185 cephalopathy, 277-280 Spasms, 71-74, 323 533-535 RFLP, 168-172 SPECT, 208-212, 217-218, 509-513 Transfer ribonucleic acid**” gene, Yale Global Tic Severity Scale, Rhombic lip, 574-582 Spectrometry, 524-528, S4-S8 610-613 316-319 Child Neurologist Please take a moment to consider an exciting Child Neurology opportunity that is now available with one of the nation’s largest freestanding children’s hospitals. Live in a beautiful, affordable area of California with easy access to the Sierra Mountains, Yosemite National Park and the Pacific Coast. This brand new 220-bed, state-of-the-art facility services a population of approximately 1 million children. Practice with another Child Neurologist and a team of physicians dedicated to pediatric care. Sub-specialties include neurosurgery, cardiology, orthopedics, trauma and many more. Highly competitive compensation package including malpractice coverage, excellent retirement, healthcare and annual leave benefits. Academic affiliation available. For more information please call, Clint Scott, MDA, 1-800-932-1023 ext.247, fax C.V. to 972-481-1333 or e-mail to [email protected].

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