Found: 23
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Temporal discrimination, a cervical dystonia endophenotype: Penetrance and functional correlates.
- Published in:
- Movement Disorders, 2014, v. 29, n. 6, p. 804, doi. 10.1002/mds.25822
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- Publication type:
- Article
The endophenotype and the phenotype: Temporal discrimination and adult-onset dystonia.
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- Movement Disorders, 2013, v. 28, n. 13, p. 1766, doi. 10.1002/mds.25676
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- Publication type:
- Article
Pregabalin- and gabapentin-associated myoclonus in a patient with chronic renal failure.
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- Movement Disorders, 2009, v. 24, n. 13, p. 2028, doi. 10.1002/mds.22286
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- Publication type:
- Article
Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-Ataxia syndrome.
- Published in:
- Movement Disorders, 2009, v. 24, n. 8, p. 1245, doi. 10.1002/mds.22267
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- Publication type:
- Article
Did Géricault's "Madwoman Obsessed With Gambling" have Parkinson's disease?
- Published in:
- 2007
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- Publication type:
- journal article
NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach.
- Published in:
- 2006
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- Publication type:
- journal article
The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.
- Published in:
- 2006
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- Publication type:
- research
UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.
- Published in:
- 2005
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- Publication type:
- journal article
Clinical spectrum of AIFM1‐associated disease in an Irish family, from mild neuropathy to severe cerebellar ataxia with colour blindness.
- Published in:
- Journal of the Peripheral Nervous System, 2019, v. 24, n. 4, p. 348, doi. 10.1111/jns.12348
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- Publication type:
- Article
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress.
- Published in:
- Journal of Neurochemistry, 2006, v. 98, n. 1, p. 156, doi. 10.1111/j.1471-4159.2006.03845.x
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- Publication type:
- Article
G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 19, p. 4201, doi. 10.1093/hmg/dds244
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- Publication type:
- Article
Cervical dystonia: a disorder of the midbrain network for covert attentional orienting.
- Published in:
- Frontiers in Neurology, 2014, v. 5, p. 1, doi. 10.3389/fneur.2014.00054
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- Publication type:
- Article
Commentary: The Fidgety Man with the Skin Rash.
- Published in:
- Movement Disorders Clinical Practice, 2021, v. 8, p. S49, doi. 10.1002/mdc3.13298
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- Publication type:
- Article
Pseudomonoballismus in a Deafferented Arm Following Combined Medullary and Cerebellar Lesions of the Proprioceptive Pathways.
- Published in:
- Movement Disorders Clinical Practice, 2017, v. 4, n. 3, p. 455, doi. 10.1002/mdc3.12417
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- Publication type:
- Article
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.
- Published in:
- Brain: A Journal of Neurology, 2005, v. 128, n. 12, p. 2786, doi. 10.1093/brain/awh667
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- Publication type:
- Article
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations.
- Published in:
- Brain: A Journal of Neurology, 2004, v. 127, n. 12, p. 2657, doi. 10.1093/brain/awh303
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- Publication type:
- Article
Commentary on “A genome wide linkage disequilibrium screen in Parkinson’s disease”.
- Published in:
- Journal of Neurology, 2005, v. 252, n. 5, p. 603, doi. 10.1007/s00415-005-0707-1
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- Publication type:
- Article
A heterozygous effect for PINK1 mutations in Parkinson's disease?
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- Annals of Neurology, 2006, v. 60, n. 4, p. 414
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- Publication type:
- Article
UCHL‐1 is not a Parkinson's disease susceptibility gene.
- Published in:
- Annals of Neurology, 2006, v. 59, n. 4, p. 627
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- Publication type:
- Article
The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism.
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- Annals of Neurology, 2004, v. 56, n. 3, p. 329
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- Publication type:
- Article
A functional polymorphism regulating dopamine β‐hydroxylase influences against Parkinson's disease.
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- Annals of Neurology, 2004, v. 55, n. 3, p. 443
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- Publication type:
- Article
The role of pathogenic DJ-1 mutations in Parkinson's disease.
- Published in:
- Annals of Neurology, 2003, v. 54, n. 3, p. 283
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- Publication type:
- Article
Parkin Disease.
- Published in:
- JAMA Neurology, 2013, v. 70, n. 5, p. 571, doi. 10.1001/jamaneurol.2013.172
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- Publication type:
- Article