Found: 30
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Neurological symptoms in patients with biopsy proven celiac disease.
- Published in:
- Movement Disorders, 2009, v. 24, n. 16, p. 2358, doi. 10.1002/mds.22821
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- Publication type:
- Article
Comparison of three clinical rating scales in Friedreich ataxia (FRDA).
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- Movement Disorders, 2009, v. 24, n. 12, p. 1779, doi. 10.1002/mds.22660
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- Publication type:
- Article
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.
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- Movement Disorders, 2006, v. 21, n. 10, p. 1734, doi. 10.1002/mds.21031
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- Publication type:
- Article
Spinocerebellar ataxia type 1, 2, and 3 and restless legs syndrome: Striatal dopamine D2 receptor status investigated by [<sup>11</sup>C]raclopride positron emission tomography.
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- Movement Disorders, 2006, v. 21, n. 10, p. 1667, doi. 10.1002/mds.20978
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- Publication type:
- Article
Cognitive function in multiple system atrophy of the cerebellar type.
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- Movement Disorders, 2006, v. 21, n. 6, p. 772, doi. 10.1002/mds.20802
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- Publication type:
- Article
UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.
- Published in:
- 2005
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- Publication type:
- journal article
CD8<sup>+</sup>/perforin<sup>+</sup>/granzyme B<sup>+</sup> effector cells infiltrating cerebellum and inferior olives in gluten ataxia.
- Published in:
- Neuropathology, 2010, v. 30, n. 1, p. 92, doi. 10.1111/j.1440-1789.2009.01042.x
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- Publication type:
- Article
Nerve Conduction Studies in Multiple System Atrophy.
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- European Neurology, 2000, v. 43, n. 4, p. 221, doi. 10.1159/000008179
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- Publication type:
- Article
Monitoring progression in Friedreich ataxia ( FRDA): the use of clinical scales.
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- Journal of Neurochemistry, 2013, v. 126, p. 118, doi. 10.1111/jnc.12318
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- Publication type:
- Article
Spinocerebellar ataxia type 1 (SCA1): Phenotype-genotype correlation studies in intermediate alleles.
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- European Journal of Human Genetics, 2002, v. 10, n. 3, p. 204
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- Publication type:
- Article
Spectrin mutations cause spinocerebellar ataxia type 5.
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- Nature Genetics, 2006, v. 38, n. 2, p. 184, doi. 10.1038/ng1728
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- Publication type:
- Article
The comorbidity and co-medication profile of patients with progressive supranuclear palsy.
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- Journal of Neurology, 2024, v. 271, n. 2, p. 782, doi. 10.1007/s00415-023-12006-4
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- Publication type:
- Article
Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein.
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- Cerebellum, 2007, v. 6, n. 4, p. 300, doi. 10.1080/14734220601136177
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- Publication type:
- Article
Cognition in hereditary ataxia.
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- Cerebellum, 2007, v. 6, n. 3, p. 280, doi. 10.1080/14734220601115924
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- Publication type:
- Article
Multiple system atrophy of the cerebellar type (MSA-C) with concomitant beta-amyloid and tau pathology.
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- Clinical Neuropathology, 2013, v. 32, n. 4, p. 286, doi. 10.5414/NP300572
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- Publication type:
- Article
KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients.
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- Human Mutation, 2010, v. 31, n. 2, p. 191, doi. 10.1002/humu.21165
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- Publication type:
- Article
No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra.
- Published in:
- 2015
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- Publication type:
- journal article
Mutation of the highly conserved cysteine residue 131 of the SCA14 associated PRKCG gene in a family with slow progressive cerebellar ataxia.
- Published in:
- Journal of Neurology, 2006, v. 253, n. 8, p. 1111, doi. 10.1007/s00415-006-0209-9
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- Publication type:
- Article
Aprataxin mutations are a rare cause of early onset ataxia in Germany.
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- Journal of Neurology, 2004, v. 251, n. 5, p. 591, doi. 10.1007/s00415-004-0374-7
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- Publication type:
- Article
Phenotypical variability of expanded alleles in the TATA-binding protein gene : Reduced penetrance in SCA17?
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- Journal of Neurology, 2003, v. 250, n. 2, p. 161, doi. 10.1007/s00415-003-0958-7
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- Publication type:
- Article
High prevalence of CSF-containing cysts in superficial hemosiderosis of the central nervous system.
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- Journal of Neurology, 2001, v. 248, n. 11, p. 1005
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- Publication type:
- Article
Restless legs syndrome in spinocerebellar ataxia types 1, 2, and 3.
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- Journal of Neurology, 2001, v. 248, n. 4, p. 311, doi. 10.1007/s004150170206
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- Publication type:
- Article
Predictors of Survival in Friedreich's Ataxia: A Prospective Cohort Study.
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- Movement Disorders, 2024, v. 39, n. 3, p. 510, doi. 10.1002/mds.29687
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- Publication type:
- Article
Antineuronal autoantibodies in neurological disorders.
- Published in:
- Biomolecular Concepts, 2011, v. 2, n. 3, p. 149, doi. 10.1515/BMC.2011.013
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- Publication type:
- Article
Onset features and time to diagnosis in Friedreich's Ataxia.
- Published in:
- 2020
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- Publication type:
- journal article
A functional polymorphism regulating dopamine β‐hydroxylase influences against Parkinson's disease.
- Published in:
- Annals of Neurology, 2004, v. 55, n. 3, p. 443
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- Publication type:
- Article
Do CTG expansions at the SCA8 locus cause ataxia?
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- Annals of Neurology, 2003, v. 54, n. 1, p. 110
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- Publication type:
- Article
Effectiveness of intravenous immunoglobin therapy in cerebellar ataxia associated with gluten sensitivity.
- Published in:
- 2001
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- Publication type:
- letter
Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 5, p. 709, doi. 10.1093/hmg/6.5.709
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- Publication type:
- Article
Screening for Proteins with Polyglutamine Expansions in Autosomal Dominant Cerebellar Ataxias.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 12, p. 1887, doi. 10.1093/hmg/5.12.1887
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- Publication type:
- Article