Found: 19
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Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia.
- Published in:
- Movement Disorders, 2012, v. 27, n. 11, p. 1451, doi. 10.1002/mds.25147
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- Publication type:
- Article
Comprehensive Genetic and Mutation Analysis of Familial Dementia with Lewy Bodies Linked to 2q35-q36.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 20, n. 1, p. 197, doi. 10.3233/JAD-2010-1356
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- Publication type:
- Article
Apathy in Parkinson's Disease: Defining the Park Apathy Subtype.
- Published in:
- Brain Sciences (2076-3425), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/brainsci12070923
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- Publication type:
- Article
Cerebellar ataxia in progressive supranuclear palsy: a clinico-pathological case report.
- Published in:
- 2021
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- Publication type:
- Letter
Left-sided hemihypomimia in Parkinson's disease.
- Published in:
- Acta Neurologica Belgica, 2011, v. 111, n. 3, p. 225
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- Publication type:
- Article
Impulsive-Compulsive Behaviours in Belgian-Flemish Parkinson's Disease Patients: A Questionnaire-Based Study.
- Published in:
- Parkinson's Disease (20420080), 2019, p. 1, doi. 10.1155/2019/7832487
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- Publication type:
- Article
Polysomnographic Predictors of Sleep, Motor, and Cognitive Dysfunction Progression in Parkinson's Disease.
- Published in:
- Current Neurology & Neuroscience Reports, 2022, v. 22, n. 10, p. 657, doi. 10.1007/s11910-022-01226-2
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- Publication type:
- Article
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 6, p. 1001, doi. 10.1007/s00401-020-02145-7
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- Publication type:
- Article
Myoclonus and Cerebellar Ataxia Following COVID‐19.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 8, p. 974, doi. 10.1002/mdc3.13049
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- Publication type:
- Article
Reply to: The Spectrum of Movement Disorders in 18p Deletion Syndrome.
- Published in:
- Movement Disorders Clinical Practice, 2019, v. 6, n. 8, p. 731, doi. 10.1002/mdc3.12835
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- Publication type:
- Article
Spectrum of Movement Disorders in 18p Deletion Syndrome.
- Published in:
- Movement Disorders Clinical Practice, 2019, v. 6, n. 1, p. 70, doi. 10.1002/mdc3.12707
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- Publication type:
- Article
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
- Published in:
- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01121-w
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- Publication type:
- Article
The effectiveness of physiotherapy for patients with isolated cervical dystonia: an updated systematic review and meta-analysis.
- Published in:
- BMC Neurology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12883-023-03473-3
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- Publication type:
- Article
COVID19-associated new-onset movement disorders: a follow-up study.
- Published in:
- Journal of Neurology, 2023, v. 270, n. 5, p. 2409, doi. 10.1007/s00415-023-11661-x
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- Publication type:
- Article
Impulse control disorders in Parkinson's disease: an overview from neurobiology to treatment.
- Published in:
- Journal of Neurology, 2015, v. 262, n. 1, p. 7, doi. 10.1007/s00415-014-7361-4
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- Publication type:
- Article
Mindfulness Training among Individuals with Parkinson’s Disease: Neurobehavioral Effects.
- Published in:
- Parkinson's Disease (20420080), 2015, v. 2015, p. 1, doi. 10.1155/2015/816404
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- Publication type:
- Article
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.
- Published in:
- Human Mutation, 2009, v. 30, n. 7, p. 1054, doi. 10.1002/humu.21007
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- Publication type:
- Article
A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies.
- Published in:
- JAMA Neurology, 2013, v. 70, n. 6, p. 727, doi. 10.1001/jamaneurol.2013.1925
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- Publication type:
- Article
Editorial: Prodromal Parkinson's Disease.
- Published in:
- 2021
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- Publication type:
- Editorial