A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Spinal Muscular Atrophy
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Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
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A Middle-aged Woman with Severe Scoliosis and Encephalopathy
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Molybdenum Cofactor Deficiency
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Clinicopath Conf, Infantile Krabbe Disease
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Prader-Willi and Angelman Syndromes
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A Clinical Study of Noonan Syndrome
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Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
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Congenital Inflammatory Myopathy
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Congenital AIDS:Review of Neurological Problems
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Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
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Alexander's Disease, A Disease of Astrocytes
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Recognising & Preventing Duchenne Muscular Dystrophy
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Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
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Adverse Effects on Offspring of Maternal Alcohol Abuse During Pregnancy
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Congenital Cytomegalovirus Infection
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An Infant with Developmental Delay, Epileptic Spasms, and Acrocyanosis
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The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
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Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
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Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
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The Acquired Metabolic Disorders of the Nervous System, Cretinism and Neonatal Myxedema
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Cognitive Delay in a 7-year-old Girl
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Early Child Development and Exposure to Antiepileptic Drugs Prenatally and Through Breastfeeding
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MRI in Methylmalonic Acidemia
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Phenylketonuria
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Management Issues for Women with Epilepsy,A Review of the Literature
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The Epilepsy of Trisomy 9p
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Prenatal Alcohol Exposure and Long-Term Developmental Consequences
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
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Cognitive and Motor Development in Infants at Risk for Human Immunodeficiency Virus
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Value of Cranial Untrasound and MRI in Predicting Neurodevelopmental Outcome in Preterm Infants
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Angelman Syndrome: Clinical Profile
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