Table Of Content

PEDIATRIC NEUROLOGY Author Index Volume 21 Abu-Sheik S, 622 Elliot JL, 456 Keegan BM, 822 Nopoulos P, 506 Adams AB, 481 Epstein FJ, 742 Keene DL, 548 Nunoue T, 661 Albertini G, 566 Erzen C, 573 Khurana DS, 691 Al-Essa MA, 826 Evans MJ, 699 Kikuchi M, 496 Obonai T, 470 Al-Lozi M, 456 Kilig A, 814 Oge E, 705 Alper G, 573 Faden HS, 699 Knip M, 794 Oguz F, 814 Al-Qudah AA, 622 Felice KJ, 818 Kobayashi K, 476 Ohki S, 543 Altobelli E, 611 Ferriero DM, 788 Kobayashi M, 543 Oki J, 715, 745 Ananthakrishnan R, 538 Filiano JJ, 538 Kobayashi M, 579 Okuhara H, 638 Anastasiou AL, 843 Fiumara A, 619 Kobayashi N, 638 Okuno T, 476 Antunes NL, 492 Fujii T, 476 Koehn MA, 839 Ouchi K, 583 Aoki Y, 471 Fujimoto S, 543 Koh S, 576 Ouvrier RA, 669 Ashwal S, 626 Funayama M, 471 Komsuoglu SS, 809 Ozand PT, 826 Aydinli N, 705 Furukawa S, 583 Kontopoulos EE, 843 Ozawa Y, 471 Futagi Y, 557 Korinthenberg R, 802 Ozmen M, 705 Bale JF Jr, 836 Kotagal S, 847 Barbosa E, 429 Goh KYC, 742 Kovanlikaya A, 576 Parano E, 619 BariSi¢ N, 450 Goldenthal MJ, 538 Kudo S, 496 Parsadanian AS, 456 Barkovich AJ, 788 Gombakis NP, 843 Kulmala P, 794 Pauling KJ, 506 Barnwell AJ, 788 Greco R, 611 Pavone L, 619 Barone R, 619 Greenlee JE, 836 Lahat E, 460 Peng S-F, 652 Baumann RJ, 503, 523 Gross A, 464 Lai FF, 797 Perlman JM, 735 Bayir H, 569 Grover WD, 763 Lazarowski A, 731 Perovié D, 450 Ben-Zeev B, 460 Giindiiz E, 562 Lee W-T, 652 Pestronk A, 456 Berrak SG, 573 Legido A, 588 Petersen B, 749 Biancaniello TA, 569 Hajnal BL, 788 Leicher CR, 818 Procopis PG, 669 Bodensteiner JB, 506 Hara M, 553 Lin J-H, 652 Boyer RS, 836 Hassan AM, 548 Liow K, 836 Rabinowicz A, 731 Brooks-Kayal AR, 444 Hattori H, 658 Lischner HW, 588 Rantala H, 794 Hay J, 699 Lowry NJ, 822 Robertson RL, 691 Caliskan M, 705 Hayakawa K, 638 Lubar JF, 633 Roland EH, 648 Canpolat C, 573 Hayashi T, 583 Rotig A, 830 Casali C, 566 Hayman M, 648 Mack KJ, 763 Ryan M, 523 Chamnanvanakij S, 735 Helmers SL, 691 Madsen JR, 691 Ryan MM, 669 Champagne JR, 548 Higuchi Y, 658 Maegaki Y, 664 Chaves-Carballo E, 826 Hill A, 648 Mahoney CP, 721 Sahebkar-Moghaddam F, Chen LS, 576 Holden KR, 429, 481, 728 Majnemer A, 776 788 Chiarelli F, 611 Hoshi Y, 638 Marin-Garcia J, 538 Sahin M, 674 Ciccarelli O, 566 Hoshino H, 496 Massaro M, 731 Sandberg DI, 754 Condoluci C, 566 Huff K, 488 Matera V, 611 Sano T, 579 Connolly AM, 456 Humphreys P, 548 McMasters R, 488 Sarnat HB, 538 Conway EJ, 742 Hyoda J, 543 Michelakakis HM, 843 Savola K, 794 Cornford ME, 488 Mikati M, 764 Sciotto A, 619 Ichiyama T, 583 Mikati MA, 830 Schneider C, 749 DaRosso RC, 742 Ilhan A, 809 Miller SP, 776 Schrod L, 749 D’ Asero G, 619 Ipsiroglu OS, 739 Mitrovié Z, 450 Sela B-A, 460 de Chadarevian J-P, 588 Islak C, 562 Mitsuyoshi I, 658 Seven M, 562 DelAguila M, 721 Isumi H, 661 Miyajima T, 476 Sevlever G, 731 Devinsky O, 464 Itagakii Y, 579 Miyamoto A, 745 Shavelle RM, 626 Di Gennaro G, 566 Ito M, 476 Morelli PJ, 569 Sheth RD, 587 DiMario FJ Jr, 818 Itoh M, 471 Morgese G, 61 | Shevell MI, 776 Dimova PS, 802 Moss EM, 444 Shimada M, 500 Dlugos DJ, 444 Jacob PJ, 548 Munda S, 619 Shinnar S, 533 Duffner PK, 699 Jalava M, 533 Muszynski CA, 742 Shiraishi K, 658 Duhaime A-C, 444 Jurenié D, 450 Sidal M, 814 du Plessis AJ, 674 Nakane S, 638 Sillanpéai M, 533 Kajii N, 638 Nanba Y, 664 Simaan EM, 830 Eda I, 757 Kali S, 809 Nass R, 464 Smith SA, 847 Ehara H, 757 Kamoshida T, 496 Nelson MD Jr, 576 Smith TH, 569 Eicher DJ, 429 Katikaneni LD, 429 Nevo Y, 456 Sobajima H, 543 Eichler F, 739 Kato T, 557 Nishida A, 661 Souweidane M, 492 Eicher DJ, 429 Katsetos CD, 588 Nishikawa M, 583 Souweidane MM, 754 Ekinci G, 573 Kaye EM, 587 Nishimura K, 553 Spanaki MV, 836 850 PEDIATRIC NEUROLOGY Vol. 21 No. 5 Stéckler-Ipsiroglu S, 739 Tamaoki Y, 757 Tuncer C, 809 Whiting SE, 548 Strassburg H-M, 749 Tanaka H, 715 Tyor WR, 481 Wisoff J, 464 Strauss DJ, 626 Taratuto A, 731 Strawsburg RH, 691 Tavora L, 492 Uniivar E, 814 Yager JY, 822 Sumi K, 579 Teach SJ, 699 Yalcinkaya C, 562 Suzuki Y, 557 Titus MO, 728 Verrotti A, 611 Yamano T, 500 Swartwood JN, 633 Toft PB, 602 Vicek BW, 721 Yau K-IT, 652 Swartwood MO, 633 Togari H, 543 Yilmaz K, 705 Toribe Y, 557 Wada M, 496 Yiiksel A, 562 Tachibana Y, 745 Touma EH, 830 Wagner CL, 429 Tagawa T, 579 Trattnig S, 739 Wallace HL, 699 Takahashi S, 715, 745 Tsao P-N, 652 Wang J, 488 Zateiriou DI, 843 Takano T, 500 Tsou KY, 797 Watanabe N, 500 Zagar M, 450 Takashima S, 471, 661 Tsuji M, 658 Wei TY, 503 Zlotnik J, 460 Tamimi AF, 622 Tunaci M, 705 White JN Jr, 633 Zupanc ML, 839 Author Index 851 PEDIATRIC NEUROLOGY Subject Index Volume 21 Acidemia, hyperpipecolic, clinical, biochemical, and ra- EMG, MRI, and clinical assessment in congenital brachial diologic observations, 826 plexus palsy, 705 Aminoaciduria resulting from vigabatrin administration in Encephalitis children with epilepsy, 460 Bilateral hippocampal, caused by enteroviral infection, Asphyxia, neonatal, and use of hypothermia, 429 836 Asphyxiated term newborn, neonatal neurologic prognos- Influenza A, with movement disorder, 669 tication, 776 Mycoplasma pneumoniae, a cause of coma in the Attention-deficit-hyperactivity disorder, hypothetically absence of meningoencephalitis, 822 caused by prenatal and perinatal striatal injury?, 602 Encephalomyelitis, acute disseminated Autistic epileptiform regression, and outcome of multiple After Rocky Mountain spotted fever, 503 subpial transections, 464 And intravenous immunoglobulin therapy, 583 Enolase elevation, neuron specific, and lactate attenuation, Bell’s palsy, corticosteroid treatment, 814 543 Blood flow velocities, cerebral, in an infant with moya- Enteroviral infection, as cause of bilateral hippocampal moya disease, 739 encephalitis, 836 Book reviews Epilepsy An Atlas of Common Metabolic and Genetic Diseases: And aminoaciduria resulting from vigabatrin adminis- Mohammed A. Al-Essa, Nadia A. Sakati, and Pinar T. tration, 460 Ozand/Authors, 763 And polymicrogyria in Kabuki make-up (Niikawa- Atlas of Sleep Medicine in Infants and Children: Ste- Kuroki) syndrome, 566 phen H. Sheldon, Susan Riter, and Mark Detrojan/ Benign childhood, with centrotemporal spikes, and Editors, 847 carbamazepine-induced epilepticus negative myoclo- Genetics of Cerebrovascular Disease: Mark J. Alberts/ nus, 664 Author, 587 Childhood, and absence of glutamic acid decarboxylase Manual of Metabolic Diseases: Mohammed A. Essa and antibodies, 794 Pinar T. Ozand/Authors, 763 Drug-resistant, and efficacy of lamotrigine and vigaba- McAlpine’s Multiple Sclerosis: Alastair Compston, trin, 802 George Ebers, Hans Lassmann, Ian McDonald, Bryan Drug-resistant, and MDRI1 gene expression, associated Matthews, and Hartmut Wekerie/Authors, 587 with tuberous sclerosis, 731 Mononeuropathies: Examination, Diagnosis, and Treat- Intractable, and effect of tiagabine on spasticity, 728 ment: A. Staal, J. van Gijn, and F. Spaans, 847 Intractable, management with intravenous lidocaine and Brachial plexus palsy, congenital, clinical assessment, lidocaine tapes, 476 MRI, and EMG, 705 Refractory, and ketogenic diet, 548 Brain herniation, risk factors for developing during dia- Use and monitoring of bromides, 523 betic ketoacidosis, 721 Epilepsy syndromes and childhood-onset seizures, 533 Brain infection, fatal, with human parovirus B19, 661 Bromides, use and monitoring in epilepsy treatment, 523 Fiber-type disproportion, congenital, severe form with marked improvement, 658 Carbamazepine-induced epileptic negative myoclonus in a child with BECTS, 664 Glioma Catecholaminergic neurons in the diencephalon and basal Globular, of the tectum, 492 ganglia of SIDS, 471 Midbrain, and sympathetic storms: a variant of dience- Cavum septi pellucidi, true prevalence, 506 phalic seizures, 742 Cerebellar hypoperfusion, and developmental dysphasia, Glutamic acid decarboxylase antibodies, absence in child- 745 hood epilepsies, 794 Corpus callosotomy, MRI signal changes in the white Glycogen storage disease type II (Pompe’s disease), and matter following, 691 hydrocephalus, 674 Corticosteroid treatment of childhood Bell’s palsy, 814 Hemifacial spasm caused by pilocytic astrocytoma of the Developmental outcome and transient periventricular fourth ventricle, 754 echodensities in preterm infants, 797 Hemiplegia, alternating, 764 Diencephalic seizures, and sympathetic storms in a child Hemorrhage, extensive late-onset primary arachnoid, in a with midbrain glioma, 742 preterm infant, 735 Dysphasia, developmental, and cerebellar hypoperfusion, Herpesviruses types 6 and 7, human, and febrile seizures, 745 699 HHV-6, and sudden unexpected death in an adolescent EEG, global and complex measures of, and methylpheni- with tuberous sclerosis, 488 date effects, 633 HIV infection, and stroke, 588 EEG slowing, hyperventilation-induced, and reevaluation Hydrocephalus associated with glycogen storage disease of hypoxia theory, 638 type II (Pompe’s disease), 674 Emery-Dreifuss muscular dystrophy, mutation analysis, Hypoperfusion, cerebellar, and developmental dysphasia, 456 745 852 PEDIATRIC NEUROLOGY Vol. 21 No. 5 Hyperpipecolic acidemia, clinical, biochemical, and radio- Multiple sclerosis and interferon beta-1b, 481 logic observations, 826 Muscular dystrophy, Emery-Dreifuss, and mutation anal- Hypothermia, use in treatment of neonatal asphyxia?, 429 ysis, 456 Hypoxia theory as the mechanism of hyperventilation- Myoclonus, epileptic negative, induced by carbamazepine induced EEG slowing, 638 in a child with BECTS, 664 Hypoxic insult, neonatal, and development of spinal mo- Myxoma, left atrial, presenting as a cerebrovascular acci- toneurons in rats, 715 dent, 569 Immunoglobulin therapy, intravenous, in acute dissemi- Neonatal asphyxia, and use of hypothermia, 429 nated encephalomyelitis, 583 Neonatal hypoxic insult, and development of spinal mo- Interferon beta-1b and multiple sclerosis, 481 torneurons in rats, 715 Neurologic prognostication, neonatal, and the asphyxiated Jervell and Lange-Nielsen syndrome, neurologic and car- term newborn, 776 diologic evaluation, 809 Neuropathy Critical illness, in pediatric intensive care patients, 749 Kabuki make-up (Niikawa-Kuroki) syndrome, with epi- Hereditary, with liability to pressure palsies, 818 lepsy and polymicrogyria, 566 Nerve injuries, war and accidental, 450 Kearns-Sayre syndrome, unusual presentation in early Nerve palsy, newborn radial, 648 childhood8,30 Niikawa-Kuroki syndrome (Kabuki make-up) with epi- Ketoacidosis, diabetic, risk factors for developing brain lepsy and polymicrogyria, 566 herniation during, 721 Nonconvulsive status epilepticus in a child with congenital Ketogenic diet in treatment of refractory epilepsy, 548 bilateral perisylvian syndrome, 579 Lactate attenuates neuron specific enolase elevation in Oculo-encephalo-hepato-renal syndrome, 757 newborn rats, 543 Lamotrigine and vigabatrin, efficacy in drug-resistant Parovirus B19 infection, human, and fetal brain infection, epilepsies, 802 661 Landau-Kleffner syndrome, 464 Perinatal depression, early prediction of neurologic out- Language-related cognitive declines after left temporal come after, 788 lobectomy, 444 Peripheral lymphocyte subsets and other immune aspects Leukodystrophy, late-infantile metachromatic, serial neu- in Rett syndrome, 619 rophysiology and MRI, 843 Perisylvian syndrome, congenital bilateral, and noncon- Lidocaine, intravenous, and lidocaine tapes, for manage- vulsive status epilepticus, 579 ment of intractable epilepsy, 476 Periventricular echodensities, transient, and developmen- Life expectancy and median survival time in permanent tal outcome in preterm infants, 797 vegetative state, 626 Pilocytic astrocytoma of the fourth ventricles, as cause of Lobectomy, left temporal, and language-related cognitive hemifacial spasm, 754 declines, 444 Platelet count and function in children receiving sodium valproate, 61 1 MDRI1 gene expression and drug-resistant epilepsy, asso- Polymicrogyria and epilepsy in Kabuki make-up (Ni- ciated with tuberous sclerosis, 731 ikawa-Kuroki) syndrome, 566 Meningoencephalitis, absence of, and coma caused by Pompe’s disease, and hydrocephalus, 674 Mycoplasma pneumoniae, 822 Pressure palsies, and hereditary neuropathy, 818 Metachromatic leukodystrophy, late-infantile, serial neu- Preterm infant, and extensive late-onset primary arachnoid rophysiology and MRI, 843 hemorrhage, 735 Methotrexate treatment, intrathecal, anterior lumbosacral Pseudotumor cerebri, retropharyngeal rhabdomyosarcoma radiculopathy after, 576 mimicking, 496 Methylphenidate effects on global and complex measures of EEG, 633 Mitochondrial defects, skeletal muscle, in non-specific Radiculopathy, anterior lumbosacral, after intrathecal neurologic disorders, 538 methotrexate treatment, 576 Rasmussen’s syndrome, unusual presentation and MRI Monoamine metabolism, pathogenic role in complex febrile seizures, 553 findings, 839 Rett syndrome, peripheral lymphocyte subsets and other Motoneurons, spinal, development in rats after a neonatal hypoxic insult, 715 immune aspects, 619 Movement disorders, and influenza A encephalitis, 669 Rhabdomyosarcoma, retropharyngeal, mimicking pseudo- Moyamoya disease, and cerebral blood flow velocities, tumor cerebri, 496 739 Rocky Mountain spotted fever, and acute disseminated MRI encephalomyelitis, 503 And Rasmussen’s syndrome, 839 And serial neurophysiology in late-infantile metachro- Sandhoff disease, neuroimaging findings, 562 matic leukodystrophy, 843 Sclerotic lesions, hypointense multiple, disappearance on EMG, and clinical assessment in congenital brachial FLAIR MRI, 500 plexus palsy, 705 Seizures FLAIR, disappearance of hypointense multiple sclerotic Childhood-onset, and epilepsy syndromes, 533 lesions on, 500 Complex febrile, and pathogenic role of monoamine Signal changes in the white matter after corpus callo- metabolism, 553 sotomy, 691 Febrile, and human herpes virus type 6 and 7, 699 Subject Index 853 SIDS, and catecholaminergic neurons in the diencephalon Tremor, neurologic outcomes within the first year of life, and basal ganglia, 471 557 Sinus thrombosis, neonatal cerebral venous, and power Tuberous sclerosis Doppler ultrasound imaging, 652 And sudden unexpected death associated with HHV-6, Sodium valproate therapy, platelet count and function, 61 | 488 Spasticity in children with intractable epilepsy, and effect Associated with MDRI gene expression and drug- of tiagabine, 728 resistant epilepsy, 731 Status epilepticus, nonconvulsive, in a child with congenital bilateral perisylvian syndrome, 579 Ultrasound imaging, power Doppler, in neonatal cerebral Striatal injury, prenatal and perinatal, a hypothetical cause venous sinus thrombosis, 652 of attention-deficit—hyperactivity disorder?, 602 Subpial transections, multiple, for autistic epileptiform Valproate therapy, sodium, platelet count and function, regression, 464 611 Sudden infant death syndrome, catecholaminergic neurons Vegetative state, permanent, life expectancy and median in the diencephalon and basal ganglia, 471 survival time, 626 Sympathetic storms in a child with a midbrain glioma: a Video electroencephalographic monitoring, short duration variant of diencephalic seizures, 742 outpatient, diagnostic value of, 622 Vigabatrin, Thrombocytopenia, associated with sagittal sinus throm- And aminoaciduria resulting in children with epilepsy, bosis, 573 460 Thrombosis, sagittal sinus, associated with thrombocyto- And lamotrigine, efficacy in drug-resistant epilepsies, 802 penia, 573 Tiagabine, effect on spasticity in children with intractable White matter, and MRI signal changes after corpus callo- epilepsy, 728 sotomy, 691 854 PEDIATRIC NEUROLOGY Vol. 21 No. 5