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Cerebral Infarcts with Arterial Occlusion in Neonates
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Neurological Involvement in the Epidermal Naevus Syndrome
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Mental Retradation Due to Germinal Matrix Infarction
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Cerebrovascular Accidents in Patients with Congenital Heart Disease
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The Tuberous Sclerosis Complex
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
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Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
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Rubella, Clinical Manifestations & Management
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An 11-year-old Boy with Language Disorder and Epilepsy
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Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
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The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
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Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
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Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
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Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
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Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
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Extension of the Clinical Spectrum of Danon Disease
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Overview of Phenylketonuria
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Mirror Writing: Neurological Reflections on an Unusual Phenomenon
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Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
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Developmental Neurotoxivity of Industrial Chemicals
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Gray Matter Heterotopia
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Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Prader-Willi and Angelman Syndromes
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Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
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MRI of White Matter Changes in the Sjogren-Larsson Syndrome
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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The Epilepsy of Trisomy 9p
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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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A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996
Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995
Rapid Antibody Test for Fragile X Syndrome
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Neurologic Abnormalities in Murderers
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