Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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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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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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CAG Repeat Expansion in Huntington Disease Determines Age at Onset in a Fully Dominant Fashion
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Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010
The Association of CAG Repeat Length with Clinical Progression in Huntington Disease
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Jaw Drop in Kennedy's Disease
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Family History and DNA Analysis in Patients With Suspected Huntington's Disease
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iH NMR Spectroscopy Studies of Huntington's Disease, Correlations with CAG Repeat Numbers
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Patients with Features Similar to Huntington's Disease, Without CAG Expansion in Huntingtin
Neurol 51:215-220, Rosenblatt,A.,et al, 1998
Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998
CAG Repeat Number Governs the Development Rate of Pathology in Huntington's Disease
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Genetic Testing of Children at Risk for Huntington's Disease
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Relationship Between Trinucleotide Repeats and Neuropathological Changes in Huntington's Disease
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Trinucleotide Repeat Length and Clinical Progression in Huntington's Disease
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Psychiatric Symptoms Do Not Correlate with Cognitive Decline, Motor Sympt or CAG Repeat Length in Huntington's
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Motor Changes in Presymptomatic Huntington Disease Gene Carriers
Arch Neurol 53:487-492, Siemers,E.,et al, 1996
Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
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Correlations Between Triplet Repeat Expansion and Clinical Features in Huntington's Disease
Arch Neurol 113:749-753, Claes,S.,et al, 1995
Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995
Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
Lancet 344:714-717, Davis,M.B.,et al, 1994
Trinucleotide Repeat Expansion in Neurological Disease
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