A 6-Year-Old Girl with Progressive Toe Walking
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A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
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Huntington Disease: Clinical Features and Diagnosis
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Recent Insights into Cerebral Cavernous Malformations: The Molecular Genetics of CCM
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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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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Dopamine-Responsive Dystonia
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Neuroblastoma -- from Genetic Profiles to Clinical Challenge
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Learning Disability
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Clinical Spectrum of CADASIL:A Study of 7 Families
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Advances in Molecular Analysis of Fragile X Syndrome
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Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
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Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
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Angelman Syndrome: Clinical Profile
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Mental Retardation in Turner Syndrome
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Genetic Linkage in Neurologic Diseases
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Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
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Corneal Opacification in Infancy
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