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Spinal Muscular Atrophy
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Spinal Muscular Atrophy A Timely Review
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Genetic Aspects of Alzheimer Disease
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Neurofibromatosis Type 2
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Neurofibromatosis
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Multiple Sclerosis
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What Level of Care for the Neurofibromatoses?
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The Genetics of Alzheimer Disease, Current Status and Future Prospects
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Trinucleotide Repeat Expansion in Neurological Disease
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Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
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Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
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Lisch Nodules in Neurofibromatosis Type I
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Familial Spinal Neurofibromatosis:Clinical and DNA Linkage Analysis
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Neurofibromatosis Type I in Children
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Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
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Occurrence of Both Neurofibromatosis 1 and 2 in the Same Individual with a Rapidly Progressive Course
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Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
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The Diagnosis of Neurofibromatosis-1 in the Child Under the Age of 6 Years
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Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
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Neurofibromatosis
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Genetic Markers for Neurofibromatosis
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Neurofibromatosis
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Mendelian Etiologies of Stroke
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Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
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Von Recklinghausen Neurofibromatosis
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981
A Family with Hereditary Ataxia:HLA Typing
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Dominant Spinopontine Atrophy
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Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
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Meningiomas in Five Members of a Family Over Two Generations, in One Member Simultaneously with Acoustic Neurinomas
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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Muscle Fiber-Type Disproportion
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Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
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Nerve-Growth Factor in Familial Dysautonomia
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