Vigabatrin in refractory epilepsy in adults and its application in children.

Abstract:

:Vigabatrin has been studied in adult drug-resistant epilepsy since 1982 in single-blind and double-blind studies followed by long-term, open evaluations. These studies have provided evidence that vigabatrin is a potent and well-tolerated antiepileptic drug and support its potential value in pediatric epilepsy. The lack of any evidence of human neurotoxicity in these patients is also reassuring regarding its use in children.

journal_name

J Child Neurol

authors

Dam M

subject

Has Abstract

pub_date

1991-01-01 00:00:00

pages

S25-9

eissn

0883-0738

issn

1708-8283

journal_volume

Suppl 2

pub_type

杂志文章,评审
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    abstract::The authors reviewed the medical records of very low-birth-weight infants admitted from 1998 to 2007 and compared neurodevelopmental outcomes with their previously reported data from 1989 to 1997. The recent group included 824 infants, and the previous group included 471 infants. Neurodevelopmental outcomes were class...

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    doi:10.1177/0883073811408606

    authors: Jang DH,Sung IY,Jeon JY,Moon HJ,Kim KS,Kim EA,Lee BS

    更新日期:2011-11-01 00:00:00

  • Identification of a novel DHCR7 mutation in a Korean patient with Smith-Lemli-Opitz syndrome.

    abstract::Smith-Lemli-Opitz syndrome is a unique malformation syndrome characterized by a defect in cholesterol biosynthesis, which is very rare among populations in Middle and East Asia. The authors identified compound heterozygous mutations ([p.Arg352Trp] + [p.Lys376ArgfsX37]) in a Korean girl with clinical and laboratory fea...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073807307099

    authors: Jong Hee Chae,Ki Joong Kim,Yong Seung Hwang,Ki CS,Kim JW

    更新日期:2007-11-01 00:00:00

  • Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome.

    abstract::Paroxysmal kinesigenic dyskinesia is a rare episodic movement disorder that can be isolated or associated with benign infantile seizures as part of choreoathetosis syndrome. Mutations in the PRRT2 gene have been recently identified as a cause of paroxysmal kinesigenic dyskinesia and infantile convulsion and choreoathe...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814556887

    authors: Zhang LM,An Y,Pan G,Ding YF,Zhou YF,Yao YH,Wu BL,Zhou SZ

    更新日期:2015-09-01 00:00:00

  • Sphenoid sinusitis masquerading as migraine headaches in children.

    abstract::The sphenoid sinus is often referred to as the "neglected sinus." Isolated sphenoid sinusitis is a rare disease with potentially devastating complications. It occurs at an incidence of about 2.7% of all sinus infections. Although headache is the most common presenting symptom, there is no typical headache pattern. Thr...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101601203

    authors: Ng YT,Butler IJ

    更新日期:2001-12-01 00:00:00

  • Clinical diversity in acute necrotizing encephalopathy.

    abstract::Acute necrotizing encephalopathy is a novel disease entity, proposed by Mizuguchi et al in 1995, that shows a characteristic selective and symmetric involvement of the thalamus, brain stem, and cerebellum. It usually leaves sequelae. The etiology of acute necrotizing encephalopathy is unknown. We describe here six pat...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400407

    authors: Yoshikawa H,Watanabe T,Abe T,Oda Y

    更新日期:1999-04-01 00:00:00

  • Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case.

    abstract::Myoclonus epilepsy with ragged red fibers (MERRF) is one of the major mitochondrial encephalomyopathies. Its main clinical features are myoclonus epilepsy, ataxia, and myopathy with ragged red fibers. Whereas there is a close correlation between MERRF syndrome and the A8344G mutation of mitochondrial DNA, the reverse ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738060210010901

    authors: Orcesi S,Gorni K,Termine C,Uggetti C,Veggiotti P,Carrara F,Zeviani M,Berardinelli A,Lanzi G

    更新日期:2006-01-01 00:00:00

  • Trends with corticosteroid use in males with Duchenne muscular dystrophy born 1982-2001.

    abstract::This study examines trends in corticosteroid use for males with Duchenne muscular dystrophy by birth year, race/ethnicity, and knowledge of Duchenne muscular dystrophy family history. Firstborn males (n = 521) selected from a population-based surveillance system of Duchenne muscular dystrophy were analyzed using Kapla...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813517263

    authors: Fox DJ,Kumar A,West NA,DiRienzo AG,James KA,Oleszek J,Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet).

    更新日期:2015-01-01 00:00:00

  • Autism Phenotypes in Tuberous Sclerosis Complex: Diagnostic and Treatment Considerations.

    abstract::Tuberous sclerosis complex is a multisystem, chronic genetic condition characterized by systemic growth of benign tumors and often accompanied by epilepsy, autism spectrum disorders, and intellectual disability. Nonetheless, the neurodevelopmental phenotype of these patients is not often detailed. The authors describe...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073815600871

    authors: Gipson TT,Poretti A,Thomas EA,Jenkins KT,Desai S,Johnston MV

    更新日期:2015-12-01 00:00:00

  • Convection-enhanced delivery for the treatment of pediatric neurologic disorders.

    abstract::Direct perfusion of specific regions of the central nervous system by convection-enhanced delivery is becoming more widely used for the delivery of compounds in the research and treatment of various neural disorders. In contrast to other currently available central nervous system delivery techniques, convection-enhanc...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073808321064

    authors: Song DK,Lonser RR

    更新日期:2008-10-01 00:00:00

  • Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter.

    abstract::Recently, a new disease entity has been defined: the disease of vanishing white matter. This leukoencephalopathy has an autosomal-recessive mode of inheritance. No cause or biochemical marker is known. We studied cerebrospinal fluid amino acids in five patients with the disease and found a consistent, moderate elevati...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901401108

    authors: van der Knaap MS,Wevers RA,Kure S,Gabreëls FJ,Verhoeven NM,van Raaij-Selten B,Jaeken J

    更新日期:1999-11-01 00:00:00

  • Child neurologists as health care surrogate for imperiled children.

    abstract::We explored child neurologists' attitudes toward taking on the role of health care surrogate for terminally ill children. Physician members of the Child Neurology Society were sent a 16-question survey via email. Of the assumed 1050 recipients, 116 (11%) answered the questionnaire. Most individuals who have been in pr...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810380048

    authors: Weisleder P,Perkins E,McLaughlin A

    更新日期:2011-03-01 00:00:00

  • Event-related potentials (P300) in primary headache in childhood and adolescence.

    abstract::There is strong evidence for a loss of habituation during cognitive processing in migraine as measured by P300 and contingent negative variation in adults. Event-related potentials evoked by an oddball paradigm have not yet been studied in children and adolescents suffering from different primary headache types. We re...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389801300703

    authors: Evers S,Bauer B,Grotemeyer KH,Kurlemann G,Husstedt IW

    更新日期:1998-07-01 00:00:00

  • Coexistent central and peripheral nervous system involvement in a Charcot-Marie-Tooth syndrome X-linked patient.

    abstract::A 14-year-old boy with an episode of acute weakness resembling acute demyelinating encephalomyelitis and polyradiculoneuritis after a febrile illness is described. Molecular analysis showed a mutation at codon 164 of the connexin 32 gene. Neuroradiological and neurophysiological follow-up is reported during acute and ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809344119

    authors: Fusco C,Frattini D,Pisani F,Spaggiari F,Ferlini A,Della Giustina E

    更新日期:2010-06-01 00:00:00

  • Gelastic seizure with tectal tumor, lobar holoprosencephaly, and subependymal nodules: clinical report.

    abstract::Gelastic seizures are characterized by inappropriate, stereotyped laughter and are often first recognized when other epileptic manifestations occur. They are frequently associated with hypothalamic hamartomas. Central nervous system developmental abnormalities are rarely reported with gelastic seizures. There is only ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700215

    authors: Akman CI,Schubert R,Duran M,Loh J

    更新日期:2002-02-01 00:00:00

  • Electroretinography and Visual Evoked Potentials in Childhood Brain Tumor Survivors.

    abstract::This population-based cross-sectional study evaluates the clinical value of electroretinography and visual evoked potentials in childhood brain tumor survivors. A flash electroretinography and a checkerboard reversal pattern visual evoked potential (or alternatively a flash visual evoked potential) were done for 51 su...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073816634863

    authors: Pietilä S,Lenko HL,Oja S,Koivisto AM,Pietilä T,Mäkipernaa A

    更新日期:2016-07-01 00:00:00

  • Alexander's disease: unique presentation.

    abstract::Subacute necrotizing encephalomyelopathy (Leigh syndrome) refers to a nebulous disease entity characterized by lactic acidosis, a wide variety a clinical manifestations, and a consistent conglomeration of pathologic findings. Several abnormalities in metabolism have been delineated in association with Leigh syndrome, ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400510

    authors: Gingold MK,Bodensteiner JB,Schochet SS,Jaynes M

    更新日期:1999-05-01 00:00:00

  • Experience in the use of the ketogenic diet as early therapy.

    abstract::The ketogenic diet has traditionally been considered an anticonvulsant therapy of last resort, despite excellent efficacy and limited side effects. We hypothesized that the ketogenic diet would have similar results in patients with new-onset epilepsy. A retrospective study was conducted of patients started on the keto...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200010501

    authors: Rubenstein JE,Kossoff EH,Pyzik PL,Vining EP,McGrogan JR,Freeman JM

    更新日期:2005-01-01 00:00:00

  • Pediatric acute transverse myelitis overview and differential diagnosis.

    abstract::Acute transverse myelitis is a clinical syndrome affecting the spinal cord, which is characterized by acute onset of motor, sensory, and autonomic dysfunction. Approximately 20% of cases of acute transverse myelitis occur in children. This review summarizes the current published literature on acute transverse myelitis...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073812452916

    authors: Wolf VL,Lupo PJ,Lotze TE

    更新日期:2012-11-01 00:00:00

  • Intrauterine endotoxin administration leads to white matter diffusivity changes in newborn rabbits.

    abstract::Maternal intrauterine inflammation has been implicated in the development of periventricular leukomalacia and white matter injury in the neonate. We hypothesized that intrauterine endotoxin administration would lead to microstructural changes in the neonatal rabbit white matter in vivo that could be detected at birth ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809338213

    authors: Saadani-Makki F,Kannan S,Makki M,Muzik O,Janisse J,Romero R,Chugani D

    更新日期:2009-09-01 00:00:00

  • Episodic migraines in children: limited evidence on preventive pharmacological treatments.

    abstract::The authors conducted a systematic literature review of preventive pharmacological treatments for episodic childhood migraines searching several databases through May 20, 2012. Episodic migraine prevention was examined in 24 publications of randomized controlled trials that enrolled 1578 children in 16 nonrandomized s...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073813488659

    authors: Shamliyan TA,Kane RL,Ramakrishnan R,Taylor FR

    更新日期:2013-10-01 00:00:00

  • Experimental Therapeutic Trial Design for Pediatric Brain Tumors.

    abstract::Pediatric brain tumors are the leading cause of cancer-related death during childhood. Since the first pediatric brain tumor clinical trials, the field has seen improved outcomes in some, but not all tumor types. In the past few decades, a number of promising new therapeutic agents have emerged, yet only a few of thes...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073815604221

    authors: Bornhorst M,Hwang EI

    更新日期:2016-10-01 00:00:00

  • Large Artery Stroke in a Child With Hypoparathyroidism.

    abstract::The association of hypoparathyroidism and ischemic stroke is rare in childhood. We report an interesting case of an 11-year-old girl diagnosed to have hypoparathyroidism and presented with an acute-onset right hemiparesis. Investigations revealed large artery ischemic stroke and uncontrolled hypoparathyroidism. Pediat...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814544366

    authors: Dhawan SR,Jondhale SN,Sahu JK,Vyas S,Singhi PD

    更新日期:2015-07-01 00:00:00

  • Neurobehavioral and neurologic outcome in long-term survivors of posterior fossa brain tumors: role of age and perioperative factors.

    abstract::We evaluated the neuropsychological and neurologic outcome of 15 long-term survivors of posterior fossa tumors who were treated between 1970 and 1984 with cranial irradiation (n = 15) and surgery (n = 14). The interval between diagnosis and evaluation ranged from 4 to 20 years (median = 10 years). Earlier age at diagn...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389501000308

    authors: Chapman CA,Waber DP,Bernstein JH,Pomeroy SL,LaVally B,Sallan SE,Tarbell N

    更新日期:1995-05-01 00:00:00

  • Transient neonatal myasthenia gravis.

    abstract::Transient neonatal myasthenia gravis is a postsynaptic neuromuscular transmission defect occurring in 21% of infants born to women with active (and, less commonly, in remission) acquired myasthenia gravis. Although passive-transfer acetylcholine receptor (AChR) antibodies are found in the majority of these newborns, t...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307389200700202

    authors: Papazian O

    更新日期:1992-04-01 00:00:00

  • Study of nerve conduction and late responses in normal Chinese infants, children, and adults.

    abstract::Healthy Chinese individuals (n = 168), aged from 24 hours to 30 years, were studied to establish the following normal values: (1) motor conduction velocity, distal latency, amplitude, and F-wave velocity in the median, ulnar, tibial, and peroneal nerves; (2) H-reflex velocity and latency in the tibial nerve for all su...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200102

    authors: Cai F,Zhang J

    更新日期:1997-01-01 00:00:00

  • Head circumference, brain weight, and tumor burden.

    abstract::The failure to diagnose an ependymoma at an appropriately early age led to an incomplete excision and a tumor burden too great for radiotherapy to control. The development of normative curves for brain weight correlated with head circumference allowed for the estimates of the extremes of possible growth rates of the t...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388600100311

    authors: Alvord EC Jr

    更新日期:1986-07-01 00:00:00

  • Cerebellar Volume in Children With Attention-Deficit Hyperactivity Disorder (ADHD).

    abstract::Attention Deficit Hyperactivity Disorder (ADHD) is associated with altered cerebellar volume and cerebellum is associated with cognitive performance. However there are mixed results regarding the cerebellar volume in young patients with ADHD. To clarify the size and direction of this effect, we conducted the analysis ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073816678550

    authors: Wyciszkiewicz A,Pawlak MA,Krawiec K

    更新日期:2017-02-01 00:00:00

  • Idiopathic "benign" intracranial hypertension: case series and review.

    abstract::Idiopathic "benign" intracranial hypertension is an uncommon but important cause of headache that can lead to visual loss. This study was undertaken to review our experience in the diagnosis and management of idiopathic intracranial hypertension, giving special attention to treatments used. A retrospective chart revie...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600701

    authors: Salman MS,Kirkham FJ,MacGregor DL

    更新日期:2001-07-01 00:00:00

  • Ambulatory electroencephalography (EEG) in children: diagnostic yield and tolerability.

    abstract::Sixty-four children, aged 0-17 years, undergoing ambulatory electroencephalography (EEG) were prospectively recruited during a 12-month period. The diagnostic yield of ambulatory electroencephalography was determined for each of the following groups: group 1: differentiation of seizures from nonepileptic events; group...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808314158

    authors: Wirrell E,Kozlik S,Tellez J,Wiebe S,Hamiwka L

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  • Cervicomedullary spinal stenosis and ventriculomegaly in a child with developmental delay due to chromosome 16p12.1 microdeletion syndrome.

    abstract::We present a case of a 1-year-old female child who was referred to the Early Intervention Clinic for evaluation of developmental delay and progressively enlarging head size. Developmental assessment revealed significant motor delay with borderline cognitive impairment. MRI of the brain revealed generalized ventriculom...

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    doi:10.1177/0883073814533149

    authors: Rai B,Sharif F

    更新日期:2015-03-01 00:00:00