Biologic Factors as Predictors of Social Outcome of epilepsy in Intellectually Normal Children:A Population-Based Study
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Strokes in Children Due to Vertebral Artery Trauma
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Risk of Intracranial Hemorrhage & Adverse Outcomes-Cocaine Expose in 323 Very Low Birth Wt Infants
J Pediatr 122:438-445, Dusick,A.M.,et al, 1993
Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
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Acquired Ocular Visual Impairment in Children, 1960-1989
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Visual Impairment in Patients with Neurofibromatosis 2
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Parietal Lobe Abnormalities Detected with MR in Patients with Infantile Autism
AJR 160:387-393, Courchesne,E.,et al, 1993
Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
Lancet 341:521-522, Matsumura,K.,et al, 1993
Alternating Hemiplegia of Childhood:A Study of 10 Pts & Results of Flunarizine Treatment
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Neuroradiological Manifestations of Focal Polymorphic Delta Activity in Children
Arch Neurol 50:181-184, Maytal,J.,et al, 1993
Electrographic Seizures in Preterm & Full-Term Neonates:Clin Corr Brain Lesions, Risk for Sequelae
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Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993
Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
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Duchenne Dystrophy:Randomized, Controlled Trial of Prednisone (18 months) & Azathioprine (12 months)
Neurol 43:520-527, Griggs,R.C.,et al, 1993
Cyclosporine Increases Muscular Force Generation in Duchenne Muscular Dystrophy
Neurol 43:527-532, Sharma,K.R.,et al, 1993
Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
NEJM 328:471-475, Shelbourne,P.,et al, 1993
Brief Report:Reverse Mutation in Myotonic Dystrophy
NEJM 328:476-480, Brunner,H.G.,et al, 1993
Genetics and Physiology of the Myotonic Muscle Disorders
NEJM 328:482-489, Ptacek,L.J.,et al, 1993
Vigabatrin in the Treatment of Infantile Spasms
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Intractable Seizures in Infancy and Early Childhood
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Hippocampal Sclerosis in Epilepsy and Childhood Febrile Seizures
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Hippocampal Sclerosis in Children with Intractable Temporal Lobe Epilepsy:Detection with MR Imaging
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Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
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Fasioscapulohumeral and Scapuloperoneal Syndromes
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Cockayne Syndrome: Review of 140 Cases
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Serial MRI in Fukuyama Type Congenital Muscular Dystrophy
Neuroradiol 34:396-398, Aihara,M.,et al, 1992
A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992
Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992
Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
J Pediatr 121:720-724, Staiano,A.,et al, 1992
Twinning and Neurologic Morbisity
Am J Dis Child 146:1110-1113, Scheller,J.M.&Nelson,K.B., 1992
Juvenile Fire Setting and the Photoparoxysmal Response
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Recurrent Status Epilepticus in Children
Ann Neurol 31:598-604, Shinnar,S.,et al, 1992
Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
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Postneonatal Vitamin B6-Dependent Epilepsy
Pediatr 90:221-223, Coker,S.B., 1992
Vascular Dysplasia in Down Syndrome:A Possible Relationship to Moyamoya Disease
Brain Dev 14:248-251, Mito,T.&Becker,L.E., 1992
Epilepsy in the First 10 Years of Life:Findings of the Child Health & Education Study
BMJ 305:857-861, Verity,C.M.,et al, 1992
Early Childhood Hepatocerebral Degeneration Misdiagnosed as Valproate Hepatotoxicity
Ann Neurol 32:767-775, Bicknese,A.R.,et al, 1992
Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992
Clin & Lab Obser Neurologic Sequelae in Transient Nonketotic Hyperglycinemia of the Neonate
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Cerebral Infarction Complicating Hemorrhagic Shock and Encephalopathy Syndrome
Pediatrics 90:626-628, Bratton,S.L.&Jardine,D.S., 1992
A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992
Infantile Panthalamic Infarct with a Striking Sonographic Finding:The"Bright Thalamus"
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A Longitudinal Assessment of Seizure Outcome and Overall Benefit From 100 Cortectomies for Epilepsy
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A prospective Study of Recurrent Febrile Seizures
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Clinicopath Conf
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Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992
Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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