Found: 22
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Comparison of techniques of botulinum toxin injections for blepharospasm and hemifacial spasm.
- Published in:
- 2019
- By:
- Publication type:
- research
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.
- Published in:
- Movement Disorders, 2009, v. 24, n. 5, p. 662, doi. 10.1002/mds.22365
- By:
- Publication type:
- Article
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia.
- Published in:
- Movement Disorders, 2008, v. 23, n. 2, p. 299, doi. 10.1002/mds.21842
- By:
- Publication type:
- Article
Parkinsonism associated with basal ganglia cryptococcal abscesses in an immunocompetent patient.
- Published in:
- Movement Disorders, 2006, v. 21, n. 5, p. 714, doi. 10.1002/mds.20789
- By:
- Publication type:
- Article
Handicap as a Measure of Perceived‐Health Status in Parkinson's Disease.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 8, p. 1172, doi. 10.1002/mdc3.13826
- By:
- Publication type:
- Article
DYT‐TUBB4A (DYT4 Dystonia): Clinical Anthology of 11 Cases and Systematized Review.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 5, p. 659, doi. 10.1002/mdc3.13452
- By:
- Publication type:
- Article
Do Patients with Progressive Supranuclear Palsy Have Episodic Memory Impairment? A Systematic Review.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 4, p. 436, doi. 10.1002/mdc3.13435
- By:
- Publication type:
- Article
Subacute Cerebellar Degeneration as the First Manifestation of Sjögren's Syndrome.
- Published in:
- Movement Disorders Clinical Practice, 2017, v. 4, n. 4, p. 637, doi. 10.1002/mdc3.12487
- By:
- Publication type:
- Article
Brief Ataxia Rating Scale: A Reliable Tool to Rate Ataxia in a Short Timeframe.
- Published in:
- Movement Disorders Clinical Practice, 2016, v. 3, n. 6, p. 621, doi. 10.1002/mdc3.12364
- By:
- Publication type:
- Article
Hearts and Minds: Emotion Recognition and Mentalizing in Parkinson's Disease and Progressive Supranuclear Palsy.
- Published in:
- Archives of Clinical Neuropsychology, 2024, v. 39, n. 4, p. 516, doi. 10.1093/arclin/acad081
- By:
- Publication type:
- Article
Amyotrophic lateral sclerosis type 8 is not a pure motor disease: evidence from a neuropsychological and behavioural study.
- Published in:
- Journal of Neurology, 2019, v. 266, n. 8, p. 1980, doi. 10.1007/s00415-019-09369-y
- By:
- Publication type:
- Article
Episodic memory in progressive supranuclear palsy: a neuropsychological and neuroimaging study.
- Published in:
- Neurological Sciences, 2022, v. 43, n. 9, p. 5363, doi. 10.1007/s10072-022-06160-2
- By:
- Publication type:
- Article
Jumpy stump triggered by tardive dyskinesia.
- Published in:
- 2013
- By:
- Publication type:
- Letter
DYT- PRKRA Mutation P222L Enhances PACT's Stimulatory Activity on Type I Interferon Induction.
- Published in:
- Biomolecules (2218-273X), 2022, v. 12, n. 5, p. 713, doi. 10.3390/biom12050713
- By:
- Publication type:
- Article
Frequency of Hereditary and GBA1‐Related Parkinsonism in Latin America: A Systematic Review and Meta‐Analysis.
- Published in:
- Movement Disorders, 2024, v. 39, n. 1, p. 6, doi. 10.1002/mds.29614
- By:
- Publication type:
- Article
Development and Validation of the Dystonia‐Pain Classification System: A Multicenter Study.
- Published in:
- Movement Disorders, 2023, v. 38, n. 7, p. 1163, doi. 10.1002/mds.29423
- By:
- Publication type:
- Article
Relationship of Genotype, Phenotype, and Treatment in Dopa‐Responsive Dystonia: MDSGene Review.
- Published in:
- Movement Disorders, 2022, v. 37, n. 2, p. 237, doi. 10.1002/mds.28874
- By:
- Publication type:
- Article
Genotype–Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review.
- Published in:
- Movement Disorders, 2021, v. 36, n. 5, p. 1086, doi. 10.1002/mds.28485
- By:
- Publication type:
- Article
Síndrome de opsoclonia-mioclonia-ataxia em paciente com AIDS.
- Published in:
- Einstein (16794508), 2013, v. 11, n. 4, p. 533, doi. 10.1590/S1679-45082013000400023
- By:
- Publication type:
- Article
Language impairment in sporadic and familial (type 8) amyotrophic lateral sclerosis: A comparative study.
- Published in:
- Muscle & Nerve, 2024, v. 70, n. 1, p. 130, doi. 10.1002/mus.28109
- By:
- Publication type:
- Article
A comparative study of cognitive and behavioral profiles between sporadic and type 8 amyotrophic lateral sclerosis.
- Published in:
- Muscle & Nerve, 2023, v. 68, n. 3, p. 316, doi. 10.1002/mus.27927
- By:
- Publication type:
- Article
POLG1 Arg953Cys mutation: Expanded phenotype and recessive inheritance in a Brazilian family.
- Published in:
- Muscle & Nerve, 2012, v. 45, n. 3, p. 453, doi. 10.1002/mus.22330
- By:
- Publication type:
- Article