GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Spinal Muscular Atrophy
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Neurodegeneration with Brain Iron Accumulation
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A Child with Arthrogryposis
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Pyruvate Dehydrogenase Deficiency (PDCD)
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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A Child with Delayed Motor Milestones and Ptosis
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Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
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Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
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Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
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MRI in Methylmalonic Acidemia
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Glycogen-Storage Disease Type II
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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An Early Marker for Neurological Deficits after Perinatal Brain Lesions
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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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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Cystic Periventricular Leukomalacia and Type of Cerebral Palsy in Preterm Infants
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Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
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A 10-Year Experience with Postpump Chorea
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Angelman Syndrome: Clinical Profile
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Congenital Inflammatory Myopathy
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Neurological Deterioration in Young Adults with Phenylketonuria
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Periventricular-Intraventricular Hemorrhage Sonographic Localization in Low Birth Weight Infants
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990
Joubert Syndrome:A Clinico-Radiological Study
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Maternal Alcohol Use During Breast-Feeding and Infant Mental and Motor Development at One Year
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Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989
Congenital AIDS:Review of Neurological Problems
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Alexander's Disease, A Disease of Astrocytes
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Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
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Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
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Congenital Ocular Motor Apraxia
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