Works matching IS 14734222 AND DT 2008 AND VI 7 AND IP 2
Results: 16
Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration.
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- Cerebellum, 2008, v. 7, n. 2, p. 138, doi. 10.1007/s12311-008-0027-y
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Magnetic resonance imaging in spinocerebellar ataxias.
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- Cerebellum, 2008, v. 7, n. 2, p. 204, doi. 10.1007/s12311-008-0025-0
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Spinocerebellar ataxias caused by polyglutamine expansions: A review of therapeutic strategies.
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- Cerebellum, 2008, v. 7, n. 2, p. 215, doi. 10.1007/s12311-008-0026-z
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Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.
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- Cerebellum, 2008, v. 7, n. 2, p. 184, doi. 10.1007/s12311-008-0053-9
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Electrophysiology in spinocerebellar ataxias: Spread of disease and characteristic findings.
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- Cerebellum, 2008, v. 7, n. 2, p. 198, doi. 10.1007/s12311-008-0024-1
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Sporadic ataxias in Japan – a population-based epidemiological study.
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- Cerebellum, 2008, v. 7, n. 2, p. 189, doi. 10.1007/s12311-008-0028-x
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SCA3: Neurological features, pathogenesis and animal models.
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- Cerebellum, 2008, v. 7, n. 2, p. 125, doi. 10.1007/s12311-008-0013-4
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Slowly progressive spinocerebellar ataxia with extrapyramidal signs and mild cognitive impairment (SCA21).
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- Cerebellum, 2008, v. 7, n. 2, p. 179, doi. 10.1007/s12311-008-0014-3
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Spinocerebellar ataxia 17 (SCA17) and Huntington’s disease-like 4 (HDL4).
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- Cerebellum, 2008, v. 7, n. 2, p. 170, doi. 10.1007/s12311-008-0016-1
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Bidirectional expression of the SCA8 expansion mutation: One mutation, two genes.
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- Cerebellum, 2008, v. 7, n. 2, p. 150, doi. 10.1007/s12311-008-0010-7
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Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1.
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- Cerebellum, 2008, v. 7, n. 2, p. 106, doi. 10.1007/s12311-008-0009-0
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Spinocerebellar ataxia 2 (SCA2).
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- Cerebellum, 2008, v. 7, n. 2, p. 115, doi. 10.1007/s12311-008-0019-y
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The highly heterogeneous spinocerebellar ataxias: From genes to targets for therapeutic intervention.
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- Cerebellum, 2008, v. 7, n. 2, p. 97, doi. 10.1007/s12311-008-0020-5
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Clinical and genetic analysis of spinocerebellar ataxia type 11.
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- Cerebellum, 2008, v. 7, n. 2, p. 159, doi. 10.1007/s12311-008-0022-3
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The clinical diagnosis of autosomal dominant spinocerebellar ataxias.
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- Cerebellum, 2008, v. 7, n. 2, p. 101, doi. 10.1007/s12311-008-0023-2
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SCA13.
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- Cerebellum, 2008, v. 7, n. 2, p. 165, doi. 10.1007/s12311-008-0039-7
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