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Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
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Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
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Neuroradiologic Findings in Marinesco-Sjogren Syndrome
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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
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Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
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The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
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Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
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Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Isolated Vitamin E Deficiency
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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The Epilepsy of Trisomy 9p
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Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
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Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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The Prevention of Neurogenetic Disease
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PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
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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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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Mitochondrial DNA and Disease
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Trinucleotide Repeat Expansion in Neurological Disease
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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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