A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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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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Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
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A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
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Melas Syndrome
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Niemann-Pick Disease Type C
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Adult-Onset Niemann-Pick Disease Type C Masquerading As Spinocerebellar Ataxias
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Complex Ataxia
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Neurodegeneration with Brain Iron Accumulation
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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Bipolar II Disorder as the Initial Presentation of CADASIL:An Underdiagnosed Manifestation
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
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Characyeristic features and progression of abnormalities on MRI for CARASIL
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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The Autosomal Recessive Cerebellar Ataxias
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Dopa-Responsive Dystonia Revisited
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Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
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Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
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Wolff-Parkinson-White Syndrome in Patients with MELAS
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Migraine and Cerebral White Matter Lesions
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Spectrum of Mutations in Biopsy-Proven CADASIL: Implications for Diagnostic Strategies
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The Inherited Ataxias and the New Genetics
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Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
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Trinucleotide Repeat Expansion in Neurological Disease
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