Found: 577
Select item for more details and to access through your institution.
Investigation of the genetic aetiology of Lewy body diseases with and without dementia.
- Published in:
- Brain Communications, 2024, v. 6, n. 4, p. 1, doi. 10.1093/braincomms/fcae190
- By:
- Publication type:
- Article
Author Correction: Microglia-synapse engulfment via PtdSer-TREM2 ameliorates neuronal hyperactivity in Alzheimer's disease models.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
Chromosome X-wide association study in case control studies of pathologically confirmed Alzheimer’s disease in a European population.
- Published in:
- Translational Psychiatry, 2024, p. 1, doi. 10.1038/s41398-024-03058-9
- By:
- Publication type:
- Article
Pathways to Primary Neurodegenerative Disease.
- Published in:
- Annals of the New York Academy of Sciences, 2000, v. 924, n. 1, p. 29, doi. 10.1111/j.1749-6632.2000.tb05556.x
- By:
- Publication type:
- Article
The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease.
- Published in:
- 2019
- By:
- Publication type:
- journal article
PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Web-based assessment of Parkinson's prodromal markers identifies GBA variants.
- Published in:
- Movement Disorders, 2015, v. 30, n. 7, p. 1002, doi. 10.1002/mds.26249
- By:
- Publication type:
- Article
H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?
- Published in:
- Movement Disorders, 2015, v. 30, n. 6, p. 828, doi. 10.1002/mds.26129
- By:
- Publication type:
- Article
Stem cell reprogramming: Basic implications and future perspective for movement disorders.
- Published in:
- Movement Disorders, 2015, v. 30, n. 3, p. 301, doi. 10.1002/mds.26113
- By:
- Publication type:
- Article
Time to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease.
- Published in:
- Movement Disorders, 2014, v. 29, n. 4, p. 454, doi. 10.1002/mds.25844
- By:
- Publication type:
- Article
Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.
- Published in:
- Movement Disorders, 2014, v. 29, n. 2, p. 245, doi. 10.1002/mds.25732
- By:
- Publication type:
- Article
Genotype and phenotype in Parkinson's disease: Lessons in heterogeneity from deep brain stimulation.
- Published in:
- Movement Disorders, 2013, v. 28, n. 10, p. 1370, doi. 10.1002/mds.25535
- By:
- Publication type:
- Article
Parkin disease and the Lewy body conundrum.
- Published in:
- Movement Disorders, 2013, v. 28, n. 6, p. 702, doi. 10.1002/mds.25486
- By:
- Publication type:
- Article
Reply to Letter: Identical twins with leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.
- Published in:
- Movement Disorders, 2013, v. 28, n. 4, p. 561, doi. 10.1002/mds.25415
- By:
- Publication type:
- Article
The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.
- Published in:
- Movement Disorders, 2013, v. 28, n. 2, p. 232, doi. 10.1002/mds.25248
- By:
- Publication type:
- Article
Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
- Published in:
- 2012
- By:
- Publication type:
- case study
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
- By:
- Publication type:
- Article
Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.
- Published in:
- Movement Disorders, 2012, v. 27, n. 10, p. 1323, doi. 10.1002/mds.24924
- By:
- Publication type:
- Article
THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations.
- Published in:
- Movement Disorders, 2012, v. 27, n. 10, p. 1290, doi. 10.1002/mds.25146
- By:
- Publication type:
- Article
Hyposmia and cognitive impairment in Gaucher disease patients and carriers.
- Published in:
- Movement Disorders, 2012, v. 27, n. 4, p. 526, doi. 10.1002/mds.24945
- By:
- Publication type:
- Article
Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course.
- Published in:
- Movement Disorders, 2012, v. 27, n. 3, p. 393, doi. 10.1002/mds.24045
- By:
- Publication type:
- Article
Syndromes of neurodegeneration with brain iron accumulation (NBIA): An update on clinical presentations, histological and genetic underpinnings, and treatment considerations.
- Published in:
- Movement Disorders, 2012, v. 27, n. 1, p. 42, doi. 10.1002/mds.23971
- By:
- Publication type:
- Article
Parkinson's disease and α-synuclein expression.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Parkinson's disease and α-synuclein expression.
- Published in:
- Movement Disorders, 2011, v. 26, n. 12, p. 2160, doi. 10.1002/mds.23948
- By:
- Publication type:
- Article
Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred).
- Published in:
- Movement Disorders, 2011, v. 26, n. 11, p. 2134, doi. 10.1002/mds.23776
- By:
- Publication type:
- Article
Milestones in PD genetics.
- Published in:
- Movement Disorders, 2011, v. 26, n. 6, p. 1042, doi. 10.1002/mds.23637
- By:
- Publication type:
- Article
Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
- Published in:
- Movement Disorders, 2010, v. 25, n. 12, p. 1791, doi. 10.1002/mds.23221
- By:
- Publication type:
- Article
Indian-subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms.
- Published in:
- Movement Disorders, 2010, v. 25, n. 10, p. 1424, doi. 10.1002/mds.23095
- By:
- Publication type:
- Article
ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation.
- Published in:
- Movement Disorders, 2010, v. 25, n. 8, p. 979, doi. 10.1002/mds.22947
- By:
- Publication type:
- Article
Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series.
- Published in:
- Movement Disorders, 2010, v. 25, n. 6, p. 771, doi. 10.1002/mds.22970
- By:
- Publication type:
- Article
GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias.
- Published in:
- Movement Disorders, 2009, v. 24, n. 11, p. 1684, doi. 10.1002/mds.22507
- By:
- Publication type:
- Article
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
Complicated recessive dystonia parkinsonism syndromes.
- Published in:
- Movement Disorders, 2009, v. 24, n. 4, p. 490, doi. 10.1002/mds.22314
- By:
- Publication type:
- Article
Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.
- Published in:
- Movement Disorders, 2009, v. 24, n. 1, p. 138, doi. 10.1002/mds.22181
- By:
- Publication type:
- Article
Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases.
- Published in:
- Movement Disorders, 2008, v. 23, n. 9, p. 1269, doi. 10.1002/mds.22078
- 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
No definitive evidence for a role for the environment in the etiology of Parkinson's disease.
- Published in:
- 2006
- By:
- Publication type:
- letter
Association of the Tau haplotype with Parkinson's disease in the Greek population.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease.
- Published in:
- Movement Disorders, 2006, v. 21, n. 6, p. 880, doi. 10.1002/mds.20814
- By:
- Publication type:
- Article
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort.
- Published in:
- Movement Disorders, 2005, v. 20, n. 12, p. 1653, doi. 10.1002/mds.20682
- By:
- Publication type:
- Article
Taiwanese cases of SCA2 are derived from a single founder.
- Published in:
- Movement Disorders, 2005, v. 20, n. 12, p. 1633, doi. 10.1002/mds.20638
- By:
- Publication type:
- Article
Parkinson's disease: A broken nosology.
- Published in:
- Movement Disorders, 2005, v. 20, n. S12, p. S2, doi. 10.1002/mds.20532
- By:
- Publication type:
- Article
Genetic testing in Parkinson's disease.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
- Published in:
- Movement Disorders, 2004, v. 19, n. 6, p. 622, doi. 10.1002/mds.20074
- By:
- Publication type:
- Article
Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations.
- Published in:
- Movement Disorders, 2004, v. 19, n. 6, p. 677, doi. 10.1002/mds.10703
- By:
- Publication type:
- Article
Parkin variants in North American Parkinson's disease: Cases and controls.
- Published in:
- Movement Disorders, 2003, v. 18, n. 11, p. 1306, doi. 10.1002/mds.10601
- By:
- Publication type:
- Article
Case-control study of the α-synuclein interacting protein gene and Parkinson's disease.
- Published in:
- Movement Disorders, 2003, v. 18, n. 11, p. 1233, doi. 10.1002/mds.10547
- By:
- Publication type:
- Article
Impact of genetic analysis on Parkinson's disease research.
- Published in:
- Movement Disorders, 2003, v. 18, n. S6, p. 96, doi. 10.1002/mds.10569
- By:
- Publication type:
- Article
Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation.
- Published in:
- 2003
- By:
- Publication type:
- journal article