Table Of Content

PEDIATRIC NEUROLOGY Author Index Volume 13 Abroms IF, 279 Fahn S, 355 Kasai K, 226 Nakai A, 346 Adelson PD, 209 Falsaperia R, 97 Kawamoto Y, 137 Nakano E, 255 Albright AL, 209 Fatal A, 235 Kikawa Y, 346 Natsume J, 61 Arai Y, 161 Finley GA, 268 Kim Y, 198 Natume J, 226 Arenas J, 69 Fitz CR, 209 Kinoshita H, 164 Needle MN, 111 Arita J, 263 Fiumara A, 97 Koeda T, 349 Negoro T, 226 Arnold DL, 327 Forssblad E, 143 Kohira R, 25 Nergardh AR, 143 Ashwal S, 269 Frank Y, 65 Konishi T, 42 Nevo Y, 235 Aso K, 226 Frohlich J, 257 Konishi Y, 134, 346 Niimi H, 323 Fuchigamai S, 25 Korenreich L, 252 Nishida K, 346 Baldwin MA, 29 Fuchigami T, 25 Kovala T, 314 Nishimura A, 25 Baram TZ, 108 Fujii Y, 134 Krach LE, 73 Noguchi Y, 25 Barrionuevo CR, 69 Fujita Y, 25 Kramer U, 235 Norman MG, 257 Barzilay Z, 83 Fukumizu M, 230 Kremenopoulos GM, 148 Nunes ML, 80, 153 Bass WT, 77 Kriel RL, 73 Bawle EV, 14 Garavaglia B, 333 Kikner S, 261 Ohki T, 226 Beck O, 143 Garcia-Silva T, 69 Kunak B, 261 Ohno K, 349 Becker CJ, 14 Gardner-Medwin D, 85 Kuno K, 61 Oki J, 175 Becker LE, 230 Garg BP, 46, 55 Kupsky WJ, 14 Okubo O, 25 Ben-Zeev B, 83 Gauthier NS, 279 Kuriyama M, 134 Okuda T, 42 Biegel JA, 111 Gilday DL, 191 Kuroda Y, 205 Ostuka T, 340 Blaser SI, 191 Glasier CM, 119 Kutai M, 235 Otero LJ, 327 Bodensteiner JB, 352 Gordon KE, 268 Lai M-W, 343 Boréus LO, 143 Griebel ML, 119 Bradley ST, 50 Gruich MJ, 50 Lange BJ, 111 Parano E, 97 Lanning M, 314 Paret G, 83 Brandt N, 83 Grunnet ML, 157 Larsen MB, 21 Parikh S, 198 Brown GK, 327 Giirer YKY, 261 Bunin GR, 111 Gutierrez M, 172 Laxer RM, 191 Pascual-Castroviejo I, 172 Leao MJ, 247 Pascual-Pascual SI, 172 Leboucg N, 169 Patel H, 55 Cabello A, 69 Haga Y, 226 Campos Y, 69 Hammer MS, 21 LeDoux MS, 5 Patron M, 172 Lee W-T, 343 Pavone L, 97 Carceller F, 172 Hanaoka S, 164 Cargan AL, 355 Hanson RA, 108 Leitner Y, 235 Percy AK, 269 Chang Y-C, 52 Harada K, 25 Lewis DW, 77 Philippart M, 268 Lissens W, 242 Phillips PC, 111 Chaves-Carballo E, 181 Harada M, 205 Logan WJ, 191 Pitt DC, 73 Chen CJ, 50 Harel S, 235 Cherry JD, 289 Hashimoto T, 205 Louis ED, 355 Pollack IF, 209 Ludman MD, 268 Poskitt KJ, 257 Chiba S, 137 Hashizume Y, 61 Lynch T, 355 Chiemchanya S, 293 Hayakawa F, 61 Chiou Y-Y, 52 Hayakawa K, 137 Rantala H, 289 Maekawa K, 263 Ciceri E, 333 Hayasaka H, 134 Ray LI, 336 Manzur AY, 257 Clark HB, 86 Hicks S, 14 Ribeiro-Silva ML, 247 Marshall PC, 279 Cohn RD, 65 Hikima A, 340 Rimoldi M, 333 Matsushima H, 263 Costa da Costa J, 80, 153 Hiyoshi K, 25 Rosemberg S, 180 Matthews PM, 327 Crichton JU, 257 Hopman JC, 319 Rotteveel JJ, 319 Mimouni M, 252 Hoppu K, 143 Russell SS, 119 Mitchell WG, 108 Rutledge SL, 5 D’ Amato CJ, 14 Horbatt Cl, 29 Mitsui T, 266 Daniéls O, 319 Horton EJ, 108 Miyamoto A, 175 Darji JT, 5 Huang C-C, 52 Miyamoto H, 323 Sadeh M, 252 da Silva LFG, 153 Humbertclaude V, 169 Miyazaki M, 205 Saino T, 175 Davis BJ, 180 Saito M, 134 Miyazato S, 323 Deguchi K, 161 Iannaccone ST, 86 Saitoh E, 266 Miyoshi H, 205 de Haan AF, 319 Ieshima A, 255 Mizuguchi M, 161 Sakao E, 323 De Meirleir L, 242 lida K, 296 Molloy PT, 111 Samuel E, 235 DeMyer WE, 46 Inyaku F, 175 Santadusit S, 293 Morikawa A, 340 Desprechins B, 242 Ito N, 137 Sarnat HB, 178 Moroni I, 333 Dobyns WB, 97 Itoh M, 255, 349 Sato S, 266 Mountz JM, 5 Iwasaki Y, 164 Muley R, 69 Schneider S, 181 Echenne BP, 169 Schoentjes E, 242 Mullaart RA, 319 Eddy AA, 191 Jones SM, 111 Seneca S, 242 Murakami M, 42 Ejiri K, 25 Severini MH, 80 Eriksson AE, 143 Kalina P, 65 Nakae Y, 263 Shen Y-Z, 343 Evans OB, 50, 336 Kaplan C, 85 Nakagawa E, 164 Sheth RD, 352 364 PEDIATRIC NEUROLOGY Vol. 13 No. 4 Shields WD, 289 Sudo M, 134 Tirosh R, 83 Wang P-J, 343 Shigematsu Y, 346 Sueoka H, 137 Tolonen U, 314 Watanabe K, 61, 226 Shiihara T, 266 Sugai K, 164 Trifiletti RR, 97 Weig SG, 279 Shimizu Y, 266 Sugita K, 323 Tsikoulas IG, 148 Wical BS, 269 Shinnar S, 235 Sunaga Y, 340 Tsutsumi H, 137 Williams JP, 119 Shuper A, 252 Swaiman KF, 198 Silver K, 327 Ueda K, 296 Yamatani M, 42 SSmiiltvhe rmRaRn, E5D5, 191 Takahashi S, 175 UUzhiaerli GM,, 323839 Yilh e S. 261 Yoneda Y, 205 Snead OC III, 108 Takanashi J, 323 Yoshimoto T, 205 Spence GT, 119 Takashima S, 161, 230, Vainionpaa L, 314 Young C, 343 Stack CV, 21 296 Vardi A, 83 Yu C-Y, 52 Stanek AE, 65 Takeshita K, 255, 349 Vedanarayanan V, 336 Steinlin MI, 191 Talwar D, 29 Visudhiphan P, 293 Stoelinga GB, 319 Tanouchi M, 205 Zafeiriou DI, 148 Storey JM, 50 Tayama M, 205 Wagner NC, 73 Zeharia A, 252 Subramony SH, 336 Thompson A, 85 Wakai S, 137 Zupanc ML, 86 PEDIATRIC NEUROLOGY Subject Index Volume 13 Acidemia, lactic, and cerebral dysgenesis, associated with Pathology of the Peripheral Nerve: Major Problems in X-linked PDH El-a subunit mutations in females, 327 Pathology: E. P. Richardson, Jr., U. DeGirolami/ Acidosis Authors Lactic, with mitochondrial myopathy, stroke-like epi- Pediatric Neuropathology: Serge Duckett/Editor sodes (MELAS) and Fanconi’s syndrome, and mito- Problems in Pediatric Drug Therapy: Louis A. Pagliaro chondrial DNA deletion, 69 and Ann M. Pagliaro/Authors Renal tubular, complicated with hypokalemic periodic Quantitative Cerebral Blood Flow Measurements Using paralysis, 52 Stable Xenon-CT: Masamichi Tomonaga, Akira ACTH, effects on brain midline structures, in infants with Tanaka, and Howard Yonas/Editors infantile spasms, 134 Textbook of Child Neurology: John H. Menkes/Author Alobar holoprosencephaly with diabetes insipidus and Brain damage of total asphyxia type (Myers), 61 neuronal migration disorder, 175 Brain, developing, a lectin and synaptophysin study, 157 Angiography, mineralizing, and hydrocephalus, hyper- Brain midline structure, effects of ACTH on, in infants cholesterolemia, and hyperlipoprotein, 257 with infantile spasms, 134 Antiphospholipid antibody syndrome in childhood stroke, 323 Apnea, isolated sleep, due to Chiari type I malformation Calcification, early onset bilateral, and epilepsy, 80 and syringomyelia, 266 Calcinosis, cerebral, and learning disabilities in hypopar- Apraxia, congenital ocular motor, in two siblings, 261 athyroidism, cause and effect or coincidence?, 252 Arteriovenous malformation vascular steal and progres- Carotid artery dissection, spontaneous extracranial ca- sive neurologic impairment, 352 rotid, 55 Ataxia, acute cerebellar, demonstrates abnormal lesions Cerebral injury, patterns of, and clinical presentation in by MRI after varicella vaccination, 340 the vascular disruptive syndrome of monozygotic twins, 279 Cerebral palsy, clues to early diagnosis of, and prospective follow-up of primitive reflex profiles in high-risk 8-amyloid precursor protein, expression of in axons of infants, 148 periventricular leukomalacia brains, 161 Chiari type I malformation and syringomyelia, with iso- Blood flow, cerebral, asymmetry of, an ultrasound Dopp- lated sleep apnea, 266 ler study in preterm newborns, 319 Child neurology, textbook of, 269 Blood flow measurements, quantitative cerebral, using Chorea, generalized, in an infant with semilobar holo- stable xenon-CT, 269 prosencephaly, 355 Book Reviews Corpus callosum, dysgenesis of, and giant interhemi- Age-Related Dopamine-Dependent Disorders: M. Seg- spheric cysts, clinical and developmental findings, awa and Y. Nomura/Editors 119 Epilepsy: 100 Elementary Principles: William H. The- Corticotropin, cerebrospinal fluid, and cortisol are re- odore and Roger J. Porter/Authors duced in infantile spasms, 108 Infantile Spasms and West Syndrome: Olivier Dulac, Cysts, giant interhemispheric, and dysgenesis of the cor- Harry T. Chugani, and Bernardo dalla Bernardina/ pus callosum, clinical and developmental findings, Editors 119 PEDIATRIC NEUROLOGY Vol. 13 No. 4 365 Dermatomyositis, treatment with high dose intravenous Immunoglobulin, high dose intravenous, for treatment of immunoglobulin, 336 dermatomyositis, 336 Developmental disorders of the nervous system, semantic Immunohistochemical study of myelination and oligoden- precision in describing, 178 drocyte in infants with periventricular leukomalacia, Diabetes insipidus and neuronal migration disorder, and 296 alobar holoprosencephaly, 175 Infantile spasms DNA deletion, mitochondrial, with mitochondrial myop- And cerebrospinal fluid corticotropin and cortisol re- athy, lactic acidosis, and stroke-like episodes duction, 108 (MELAS) and Fanconi’s syndrome, 69 And effects of ACTH on brain midline structures, 134 Dopamine-dependent disorders, age-related, 181 And West syndrome, 86 Doppler study, ultrasound, and asymmetry of the cerebral Infarction, ischemic thalamic, 46 blood flow in preterm newborns, 319 Ito hypomelanosis and moyamoya disease, 169 Drug therapy, pediatric, problems in, 181 Dysgenesis, cerebral, and lactic acidemia associated with Klippel-Feil syndrome and thenar hypoplasia due to aber- X-linked PDH El-a subunit mutations in females, 327 rant radial artery, 343 Dystonia Kluver-Bucy syndrome following heat stroke, 73 Congenital myotonic, 85 Generalized, and SPECT abnormalities, 5 Learning disabilities and cerebral calcinosis, in hypopar- Hereditary torsion, and rhabdomyolysis, 83 athyroidism, cause and effect or coincidence?, 252 Lectin and synaptophysin study of developing brain, 157 EEG, hyperventilation activation on, and epilepsy, 42 Lesions, pediatric central nervous system, and role of Epilepsy frameless stereotactic techniques in treatment, 209 100 elementary principles, 269 Leukemia, acute lymphoblastic, vincristine therapy and And early onset bilateral calcifications, 80 impairment of conduction in the entire peripheral And hyperventilation activation on EEG recording, 42 nerve, 314 Complex partial status epilepticus, 137 Leukomalacia, periventricular, immunohistochemical Intractable, flunarizine of limited value in, 143 study of myelination and oligodendrocyte, 296 Unprovoked seizures and developmental disabilities, Lupus erythematosus 235 Neurologic characteristics, 198 With meningomyelocele, 29 Systemic, and neurological manifestations, 191 Epilepticus, status, and timing of tapering of pentobarbital therapy, 164 Mazindol, effects in patients with Prader-Willi syndrome, Fabry disease, treatment of painful crises with morphine, 349 MELAS, and mitochondrial DNA deletion with mitochon- 268 drial myopathy, lactic acidosis, and Fanconi’s syn- Fanconi’s syndrome, with mitochondrial DNA deletion, mitochondrial myopathy, lactic acidosis, and stroke- drome, 69 Meningomyelocele, and epilepsy, 29 like episodes (MELAS), 69 Mental retardation, and reduced N-acetylaspartate in the Flunarizine of limited value in children with intractable epilepsy, 143 brain observed on in vivo proton magnetic resonance spectroscopy, 205 Glutaric aciduria type II, riboflavin-responsive, presenting Mitochondrial ATPase 6 gene, novel point mutation, and as a leukodystrophy, 333 bilateral striatal necrosis, 242 Guillain-Barré syndrome, and risk factors of respiratory Morphine, as treatment for painful crises of Fabry disease, 268 failure, 289 Moyamoya disease and Ito hypomelanosis, 169 MRI Holoprosencephaly, semilobar, and generalized chorea, And findings of Zellweger syndrome, 346 355 Hopkins syndrome, and T,-weighted-high intensity of an- Demonstrating abnormal lesions in acute cerebellar ataxia after varicella vaccination, 340 terior horn on spinal MR imaging, 263 Spinal, and T,-weighted-high intensity of anterior horn HSAN IV and neurotrophins, 180 in Hopkins syndrome, 263 Hydrocephalus Multiple sclerosis, recurrence and subsequent develop- Neonatal posthemorrhagic, neuropathologic and immu- ment, and optic neuritis, 293 nohistochemical studies, 230 Muscular dystrophies, congenital, 97 With mineralizing angiopathy, hypercholesterolemia, and hyperlipoprotein (a), 257 Myelination and oligodendrocyte, immunohistochemical study of in infants with periventricular leukomalacia, Hypercholesterolemia, with hydrocephalus, mineralizing 296 angiopathy, and hyperlipoprotein (a), 257 Myoclonus, neonatal segmental, associated with hyper- Hyperglycorrhachia, and neonatal segmental myoclonus, glycorrhachia, 77 Hyperlipoprotein (a), with hydrocephalus, mineralizing angiopathy, and hypercholesterolemia, 257 N-acetylaspartate, reduced, in brain observed on in vivo Hyperventilation activation on EEG recording in children magnetic resonance spectroscopy in patients with with epilepsy, 42 mental retardation, 205 Hypoparathyroidism, with cerebral calcinosis and learning Necrosis, bilateral striatal, with a novel point mutation in disabilities, cause and effect or coincidence?, 252 the mitochondrial ATPase 6 gene, 242 Hypoplasia, thenar, in Klippel-Feil syndrome due to ab- Neuritis, optic, and recurrence and subsequent develop- errant radial artery, 343 ment of multiple sclerosis, 293 366 PEDIATRIC NEUROLOGY Vol. 13 No. 4 Neuroleptic malignant syndrome in striatonigral degener- SPECT abnormalities in generalized dystonia, 5 ation, 255 Status epilepticus Neuronal migration disorder, and alobar holoprosenceph- And timing of tapering of pentobarbital therapy, 164 aly with diabetes insipidus, 175 Complex partial, 137 Neuropathology, pediatric, 86 Stereotactic techniques, frameless, and role in treatment Neurotrophins and HSAN IV, 180 of pediatric central nervous system lesions, 209 Striatonigral degeneration, and neuroleptic malignant de- Oligodendrocyte and myelination, immunohistochemical generation, 255 study of in infant with periventricular leukomalacia, Strokes, and antiphospholipid antibody syndrome, 323 296 Stroke-like episodes (MELAS), with mitochondrial my- Olivopontocerebellar atrophy, familial infantile, 14 opathy, lactic acidosis, and Fanconi’s syndrome, with Opsoclonus-myoclonus, outcome regardless of etiology, mitochondrial DNA deletion, 69 21 Synaptophysin and lectin study of developing brain, 157 Optic neuritis and recurrence and subsequent development Syringomyelia and Chiari type I malformation, with iso- of multiple sclerosis, 293 lated sleep apnea, 266 Orofaciodigital syndrome type with severe CNS defects, 247 Thenar hypoplasia in Klippel-Feil syndrome due to aberrant radial artery, 343 P300 wave, developmental changes elicited during two Tuberous sclerosis associated with histologically con- different experimental conditions, 25 firmed ocular and cerebral tumors, 172 Paralysis, hypokalemic periodic, and renal tubular acido- Tumors sis, 52 CNS of pediatric patients, and neurologic and other Pentobarbital therapy for status epilepticus, timing of ta- disorders in relatives, 111 pering, 164 Histologically confirmed ocular and cerebral, and tu- Peripheral nerve berous sclerosis, 172 Entire, vincristine therapy for children with acute lym- Malignant rhabdoid, of brain and kidney, 65 phoblastic leukemia impairs conduction in, 314 Pathology of, 86 Ultrasound Doppler study of asymmetry of cerebral blood Periventricular leukomalacia brains, and expression of flow, 319 8-amyloid precursor protein in axons of, 161 Prader-Willi syndrome, and effects of mazindol, 349 Varicella vaccination, acute cerebellar ataxia demon- Proton magnetic resonance spectroscopy, in vivo, and ob- strates abnormal lesions by MRI after, 340 servation of reduced N-acetylaspartate in the brain of Vascular disruptive syndrome of monozygotic twins, pat- patients with mental retardation, 205 terns of cerebral injury and clinical presentation, 279 Vascular steal, arteriovenous malformation, and progres- Radial artery, aberrant, and thenar hypoplasia in Klippel- sive neurologic impairment, 352 Feil syndrome, 343 Vincristine therapy for children with acute lymphoblastic Reflex profiles, primitive, prospective follow-up in high- leukemia, and impairment of conduction in the entire risk infants: clues to an early diagnosis of cerebral peripheral nerve, 314 palsy, 148 Vogt-Koyanagi-Harada syndrome, 50 Respiratory failure, risk factors of, in Guillain-Barré syndrome, 289 West syndrome Rhabdomyolysis due to hereditary torsion dystonia, 83 And infantile spasms, 86 Riboflavin-responsive glutaric aciduria type II presenting Outcome predicted by ictal, clinical, and electroenceph- as a leukodystrophy, 333 alographic features?, 226 Seizures, unprovoked, and developmental disabilities, X-linked PDH El-a subunit mutations in females, asso- 235 ciation of cerebral dysgenesis and lactic acidemia, 327 Semantic precision in describing developmental disorders of the nervous system, 178 Zellweger syndrome, MRI findings, 346 PEDIATRIC NEUROLOGY Voi. 13 No. 4 367