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Endosomal trafficking leads the way in Parkinson's disease.
- Published in:
- 2019
- By:
- Publication type:
- editorial
The emerging role of Rab GTPases in the pathogenesis of Parkinson's disease.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Double homozygous mutations (R275W and M432V) in the ParkinGene associated with late-onset Parkinson's disease.
- Published in:
- 2016
- By:
- Publication type:
- case study
Familial aggregation of Parkinson's disease in the Faroe Islands.
- Published in:
- Movement Disorders, 2015, v. 30, n. 4, p. 538, doi. 10.1002/mds.26132
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- Publication type:
- Article
Genetic variability of the retromer cargo recognition complex in parkinsonism.
- Published in:
- Movement Disorders, 2015, v. 30, n. 4, p. 580, doi. 10.1002/mds.26104
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- Publication type:
- Article
Motor phenotype of LRRK2-associated Parkinson's disease: A tunisian longitudinal study.
- Published in:
- Movement Disorders, 2015, v. 30, n. 2, p. 253, doi. 10.1002/mds.26097
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- Publication type:
- Article
DNAJC13 genetic variants in parkinsonism.
- Published in:
- Movement Disorders, 2015, v. 30, n. 2, p. 273, doi. 10.1002/mds.26064
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- Publication type:
- Article
Clinical, positron emission tomography, and pathological studies of DNAJC13 p.N855S Parkinsonism.
- Published in:
- Movement Disorders, 2014, v. 29, n. 13, p. 1684, doi. 10.1002/mds.26019
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- Publication type:
- Article
A Novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy.
- Published in:
- Movement Disorders, 2014, v. 29, n. 9, p. 1201, doi. 10.1002/mds.25833
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- Publication type:
- Article
In vivo dopaminergic and serotonergic dysfunction in DCTN1 gene mutation carriers.
- Published in:
- Movement Disorders, 2014, v. 29, n. 9, p. 1197, doi. 10.1002/mds.25893
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- Publication type:
- Article
Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.
- Published in:
- Movement Disorders, 2013, v. 28, n. 14, p. 2039, doi. 10.1002/mds.25637
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- Publication type:
- Article
Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.
- Published in:
- Movement Disorders, 2013, v. 28, n. 6, p. 811, doi. 10.1002/mds.25421
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- Publication type:
- Article
The genetics of Parkinson's disease: Progress and therapeutic implications.
- Published in:
- Movement Disorders, 2013, v. 28, n. 1, p. 14, doi. 10.1002/mds.25249
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- Publication type:
- Article
Genetic variants of α-synuclein are not associated with essential tremor.
- Published in:
- Movement Disorders, 2011, v. 26, n. 14, p. 2552, doi. 10.1002/mds.23909
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- Publication type:
- Article
Common variants in PARK loci and related genes and Parkinson's disease.
- Published in:
- Movement Disorders, 2011, v. 26, n. 2, p. 280, doi. 10.1002/mds.23376
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- Publication type:
- Article
Dopamine turnover increases in asymptomatic LRRK2 mutations carriers.
- Published in:
- Movement Disorders, 2010, v. 25, n. 16, p. 2717, doi. 10.1002/mds.23356
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- Publication type:
- Article
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa.
- Published in:
- Movement Disorders, 2010, v. 25, n. 13, p. 2052, doi. 10.1002/mds.23283
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- Publication type:
- Article
Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease.
- Published in:
- Movement Disorders, 2010, v. 25, n. 13, p. 2156, doi. 10.1002/mds.23265
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- Publication type:
- Article
LRRK2 variation and Parkinson's disease in African Americans.
- Published in:
- Movement Disorders, 2010, v. 25, n. 12, p. 1973, doi. 10.1002/mds.23163
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- Publication type:
- Article
Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population.
- Published in:
- Movement Disorders, 2009, v. 24, n. 16, p. 2411, doi. 10.1002/mds.22795
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- Publication type:
- Article
GCH1 in early-onset Parkinson's disease.
- Published in:
- Movement Disorders, 2009, v. 24, n. 14, p. 2070, doi. 10.1002/mds.22729
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- Publication type:
- Article
Expanding the clinical phenotype of SNCA duplication carriers.
- Published in:
- Movement Disorders, 2009, v. 24, n. 12, p. 1811, doi. 10.1002/mds.22682
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- Publication type:
- Article
Reply: GIGYF2 variants are not associated with Parkinson's disease in Italy.
- Published in:
- Movement Disorders, 2009, v. 24, n. 12, p. 1868, doi. 10.1002/mds.22614
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- Publication type:
- Article
Reported mutations in GIGYF2 are not a common cause of Parkinson's disease.
- Published in:
- Movement Disorders, 2009, v. 24, n. 4, p. 619, doi. 10.1002/mds.22451
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- Publication type:
- Article
FGF20 and Parkinson's disease: No evidence of association or pathogenicity via α-synuclein expression.
- Published in:
- Movement Disorders, 2009, v. 24, n. 3, p. 455, doi. 10.1002/mds.22442
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- Publication type:
- Article
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive parkinsonism.
- Published in:
- Movement Disorders, 2009, v. 24, n. 1, p. 104, doi. 10.1002/mds.22093
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- Publication type:
- Article
Common variants in Parkinson's disease.
- Published in:
- 2007
- By:
- Publication type:
- letter
ELAVL4, PARK10, and the Celts.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.
- Published in:
- 2007
- By:
- Publication type:
- journal article
The ups and downs of α-synuclein mRNA expression.
- Published in:
- Movement Disorders, 2007, v. 22, n. 2, p. 293, doi. 10.1002/mds.21223
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- Publication type:
- Article
Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred.
- Published in:
- 2007
- By:
- Publication type:
- case study
Parkinsonism, FXTAS, and FMR1 premutations.
- Published in:
- Movement Disorders, 2005, v. 20, n. 2, p. 230, doi. 10.1002/mds.20297
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- Publication type:
- Article
Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.
- Published in:
- 2004
- By:
- Publication type:
- journal 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
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- Publication type:
- Article
It's a double knock-out! The quaking mouse is a spontaneous deletion of parkin and parkin co-regulated gene (PACRG).
- Published in:
- Movement Disorders, 2004, v. 19, n. 1, p. 101, doi. 10.1002/mds.20000
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- 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
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- 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
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- Publication type:
- Article
Complex interactions in Parkinson's disease: A two-phased approach.
- Published in:
- Movement Disorders, 2003, v. 18, n. 6, p. 631, doi. 10.1002/mds.10431
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- Publication type:
- Article
Case-Control study of dopamine transporter-1, monoamine oxidase-B, and catechol- O-methyl transferase polymorphisms in Parkinson's disease.
- Published in:
- Movement Disorders, 2002, v. 17, n. 6, p. 1305, doi. 10.1002/mds.10268
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- Publication type:
- Article
Case-control study of estrogen receptor gene polymorphisms in Parkinson's disease.
- Published in:
- Movement Disorders, 2002, v. 17, n. 3, p. 509, doi. 10.1002/mds.1253
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- Publication type:
- Article
Case-control study of debrisoquine 4-hydroxylase, n-acetyltransferase 2, and apolipoprotein e gene polymorphisms in Parkinson's disease.
- Published in:
- Movement Disorders, 2000, v. 15, n. 4, p. 714, doi. 10.1002/1531-8257(200007)15:4<714::AID-MDS1018>3.0.CO;2-3
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- Publication type:
- Article
Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?
- Published in:
- Human Genetics, 2000, v. 107, n. 5, p. 476, doi. 10.1007/s004390000395
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- Publication type:
- Article
Altered dopamine release and monoamine transporters in Vps35 p.D620N knock-in mice.
- Published in:
- NPJ Parkinson's Disease, 2018, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41531-018-0063-3
- By:
- Publication type:
- Article
Whole-Exome Sequencing of an Exceptional Longevity Cohort.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Measuring dopaminergic function in the 6-OHDA-lesioned rat: a comparison of PET and microdialysis.
- Published in:
- EJNMMI Research, 2013, v. 3, n. 1, p. 1, doi. 10.1186/2191-219X-3-69
- By:
- Publication type:
- Article
Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease.
- Published in:
- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 6, p. 661, doi. 10.1001/jama.296.6.661
- By:
- Publication type:
- Article
Assessing an Interactive Online Tool to Support Parents' Genomic Testing Decisions.
- Published in:
- Journal of Genetic Counseling, 2019, v. 28, n. 1, p. 10, doi. 10.1007/s10897-018-0281-1
- By:
- Publication type:
- Article
Identification of a Novel Gene Linked to Parkin via a Bidirectional Promoter.
- Published in:
- Annals of the New York Academy of Sciences, 2003, v. 991, n. 1, p. 311, doi. 10.1111/j.1749-6632.2003.tb07493.x
- By:
- Publication type:
- Article
LRRK2 overexpression alters glutamatergic presynaptic plasticity, striatal dopamine tone, postsynaptic signal transduction, motor activity and memory.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 5, p. 1336, doi. 10.1093/hmg/ddu543
- By:
- Publication type:
- Article
Parkin genetics: one model for Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R127
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- Publication type:
- Article