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Creutzfeldt-Jakob Disease in a Young Woman
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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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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Neurodegeneration with Brain Iron Accumulation
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Huntington Disease: Clinical Features and Diagnosis
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Spinal Muscular Atrophy A Timely Review
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Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
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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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Neurologic Manifestations of von Hippel-Lindau Disease
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Dopamine-Responsive Dystonia
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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The Hereditary Spastic Paraplegias
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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Amyotrophic Lateral Sclerosis
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Hereditary Spastic Paraparesis: A Review of New Developments
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Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Facial Nerve is Liable to Pressure Palsy
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Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
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Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Natural History in Proximal Spinal Muscular Atrophy
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Location of Facioscapulohumeral Muscular Dystrophy Gene on Chromosome 4
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
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