Works matching IS 08853185 AND DT 2012 AND VI 27 AND IP 14
Results: 33
Color discrimination deficits in Parkinson's disease are related to cognitive impairment and white-matter alterations.
- Published in:
- Movement Disorders, 2012, v. 27, n. 14, p. 1781, doi. 10.1002/mds.25272
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- Publication type:
- Article
Myoclonus and dystonia in cerebrotendinous xanthomatosis.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1805, doi. 10.1002/mds.25206
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- Publication type:
- Article
Weak detrusor contractility correlates with motor disorders in Parkinson's disease.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1775, doi. 10.1002/mds.25225
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- Publication type:
- Article
Meningioma with intense I(123) FP-CIT uptake.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Toward magnetic resonance imaging biomarkers for progressive supranuclear palsy and multisystem atrophy.
- Published in:
- Movement Disorders, 2012, v. 27, n. 14, p. 1711, doi. 10.1002/mds.25196
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- Publication type:
- Article
Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
- Published in:
- 2012
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- Publication type:
- Case Study
Atypical parkinsonism and cerebrotendinous xanthomatosis: Report of a family with corticobasal syndrome and a literature review.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1769, doi. 10.1002/mds.25229
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- Publication type:
- Article
The prevalence of primary dystonia: A systematic review and meta-analysis.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1789, doi. 10.1002/mds.25244
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- Publication type:
- Article
Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1741, doi. 10.1002/mds.25295
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- Publication type:
- Article
Common variation in the LRRK2 gene is a risk factor for Parkinson's disease.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1823, doi. 10.1002/mds.25226
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- Publication type:
- Article
Seizures in juvenile Huntington's disease: Frequency and characterization in a multicenter cohort.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1797, doi. 10.1002/mds.25237
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- Publication type:
- Article
Meningioma with intense I<sup>123</sup> FP-CIT uptake.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1744, doi. 10.1002/mds.25277
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- Publication type:
- Article
DYT7 gene locus for cervical dystonia on chromosome 18p is questionable.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1820, doi. 10.1002/mds.25219
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- Publication type:
- Article
Comparison of dysphagia before and after deep brain stimulation in Parkinson's disease.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1763, doi. 10.1002/mds.25259
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- Publication type:
- Article
Respiratory disorders associated with dystonia.
- Published in:
- Movement Disorders, 2012, v. 27, n. 14, p. 1816, doi. 10.1002/mds.25269
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- Publication type:
- Article
Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
- Published in:
- Movement Disorders, 2012, v. 27, n. 14, p. 1829, doi. 10.1002/mds.25199
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- Publication type:
- Article
Long-term outcomes of surgical therapies for Parkinson's disease.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1718, doi. 10.1002/mds.25214
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- Publication type:
- Article
Huntington's disease: How intermediate are intermediate repeat lengths?
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- Movement Disorders, 2012, v. 27, n. 14, p. 1714, doi. 10.1002/mds.25172
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- Publication type:
- Article
Arkypallidal neuron: A new player in the basal ganglia circuitry.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1740, doi. 10.1002/mds.25257
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- Publication type:
- Article
A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1827, doi. 10.1002/mds.25114
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- Publication type:
- Article
Mutations in the phospholipid remodeling gene SERAC1 cause MEGDEL syndrome.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1738, doi. 10.1002/mds.25228
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- Publication type:
- Article
Book review: Marsden's Book of Movement Disorders.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1841, doi. 10.1002/mds.25268
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- Publication type:
- Article
Supranuclear gaze palsy in glycine receptor antibody-positive progressive encephalomyelitis with rigidity and myoclonus.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1833, doi. 10.1002/mds.25239
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- Publication type:
- Article
Tremor-ataxia with central hypomyelination (TACH): Dystonia as a new clinical feature.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1831, doi. 10.1002/mds.25270
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- Publication type:
- Article
Commentary for 'oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8'.
- Published in:
- Movement Disorders, 2012, v. 27, n. 14, p. 1743, doi. 10.1002/mds.25332
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- Publication type:
- Article
Imaging measures predict progression in progressive supranuclear palsy.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1801, doi. 10.1002/mds.24970
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- Publication type:
- Article
Is it all about timing?
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- Movement Disorders, 2012, v. 27, n. 14, p. 1739, doi. 10.1002/mds.25252
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- Publication type:
- Article
C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1835, doi. 10.1002/mds.25245
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- Publication type:
- Article
Sleep and Parkinson's disease: A review of case-control polysomnography studies.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1729, doi. 10.1002/mds.25197
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- Publication type:
- Article
Progression of cortical thinning in early Parkinson's disease.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1746, doi. 10.1002/mds.25240
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- Publication type:
- Article
An electromyographic study of parkinsonian swallowing and its response to levodopa.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1811, doi. 10.1002/mds.25262
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- Publication type:
- Article
Multiple system atrophy with prolonged survival.
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- Movement Disorders, 2012, v. 27, n. 14, p. 1837, doi. 10.1002/mds.25289
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- Publication type:
- Article
Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy.
- Published in:
- Movement Disorders, 2012, v. 27, n. 14, p. 1754, doi. 10.1002/mds.24968
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- Publication type:
- Article