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An 11-year-old Boy with Language Disorder and Epilepsy
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Sturge-Weber Syndrome
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Angelman Syndrome Revisited
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002
Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
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Mucolipidosis Type IV; Characteristic MRI Findings
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Bilirubin Metabolism and Kernicterus
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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Startle Provoked Epileptic Seizures:Features in 19 Patients
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
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Alternating Hemiplegia of Childhood
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Angelman Syndrome: Clinical Profile
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Epidermal Nevus Synd:A Neurologic Variant with Hemimegalencephaly, Gyral Malf, Mental Retard, Seizures & Facial Hemihyper
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Autistic and Dysphasic Children, II:Epilepsy
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Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
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Bilateral Central Macrogyria:Epilepsy, Pseudobulbar Palsy, and Mental Retardation-A Migration Disorder
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Congenital Muscular Dystrophy
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Encephalotrigeminal Angiomatosis
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Rett Syndrome:Natural History and Management
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Neurologic Manifestations of the Organoid Nevus Syndrome
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Neurological Findings in Patients with the Fragile-X Syndrome
JNNP 48:150-153, Finelli,P.F.,et al, 1985
Alexander's Disease, A Disease of Astrocytes
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Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
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Familial Spastic Paraplegia, Mental Retardation, & Precocious Puberty
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Prenatal Diagnosis of Fragile X Chromosome
Lancet 1:99-100, Shapiro,L.R.,et al, 1982
Prognostic Indicators in Hemiparetic Cerebral Palsy
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Periodic Lateralized Epileptiform Discharges in Infants & Children
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Neurological Complications of Infantile Osteopetrosis
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The Thyroid Gland:Its Relationship to Neurology
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Genetic Counseling in Retinitis Pigmentosa
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Pediatric Neurology
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Neurocutaneous Disease
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The Cornelia de Lange Syndrome
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