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Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Complete Genomic Screen in Parkinson Disease.
- Published in:
- JAMA: Journal of the American Medical Association, 2001, v. 286, n. 18, p. 2239, doi. 10.1001/jama.286.18.2239
- By:
- Publication type:
- Article
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22.
- Published in:
- 2000
- By:
- Publication type:
- journal article
Parkinson's disease variant detection and disclosure: PD GENEration, a North American study.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 8, p. 2668, doi. 10.1093/brain/awae142
- By:
- Publication type:
- Article
Genetic counseling and testing for Huntington's disease: A historical review.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 1, p. 75, doi. 10.1002/ajmg.b.32453
- By:
- Publication type:
- Article
Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study.
- Published in:
- Journal of the International Neuropsychological Society, 2011, v. 17, n. 1, p. 91, doi. 10.1017/S1355617710001190
- By:
- Publication type:
- Article
Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study.
- Published in:
- Journal of the International Neuropsychological Society, 2010, v. 17, n. 1, p. 91, doi. 10.1017/S1355617710001190
- By:
- Publication type:
- Article
Early detection of dementia in Huntington’s disease: The Predict-HD study
- Published in:
- 2005
- By:
- Publication type:
- Abstract
Sex Differences in Clinical Features of Early, Treated Parkinson’s Disease.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0133002
- By:
- Publication type:
- Article
Therapy in Huntington's Disease: Where Are We?
- Published in:
- Current Neurology & Neuroscience Reports, 2012, v. 12, n. 4, p. 359, doi. 10.1007/s11910-012-0277-4
- By:
- Publication type:
- Article
Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset.
- Published in:
- Human Genetics, 2012, v. 131, n. 12, p. 1833, doi. 10.1007/s00439-012-1205-z
- By:
- Publication type:
- Article
Huntington Disease: Clinical, Genetic, and Social Aspects.
- Published in:
- Journal of Geriatric Psychiatry & Neurology, 1998, v. 11, n. 2, p. 61, doi. 10.1177/089198879801100204
- By:
- Publication type:
- Article
Cognitive and Motor Function in Long-Duration PARKIN-Associated Parkinson Disease.
- Published in:
- JAMA Neurology, 2014, v. 71, n. 1, p. 62, doi. 10.1001/jamaneurol.2013.4498
- By:
- Publication type:
- Article
What we don't need to prove but need to do in multidisciplinary treatment and care in Huntington's disease: a position paper.
- Published in:
- Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02622-8
- By:
- Publication type:
- Article
Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 1, p. 137
- By:
- Publication type:
- Article
Beyond disgust: impaired recognition of negative emotions prior to diagnosis in Huntingtons disease.
- Published in:
- Brain: A Journal of Neurology, 2007, v. 130, n. 7, p. 1732
- By:
- Publication type:
- Article
Tools for communicating risk for Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00432-6
- By:
- Publication type:
- Article
Clinical Aspects of CAG Repeat Diseases.
- Published in:
- Brain Pathology, 1997, v. 7, n. 3, p. 881, doi. 10.1111/j.1750-3639.1997.tb00892.x
- By:
- Publication type:
- Article
Seeking clarity through the genetic lens: A work in progress.
- Published in:
- Annals of Neurology, 2003, v. 54, n. 1, p. 5
- By:
- Publication type:
- Article
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
- Published in:
- Annals of Neurology, 2003, v. 53, n. 5, p. 624
- By:
- Publication type:
- Article
End-of-life measures in Huntington disease: HDQLIFE Meaning and Purpose, Concern with Death and Dying, and End of Life Planning.
- Published in:
- Journal of Neurology, 2019, v. 266, n. 10, p. 2406, doi. 10.1007/s00415-019-09417-7
- By:
- Publication type:
- Article
Agreement between clinician-rated versus patient-reported outcomes in Huntington disease.
- Published in:
- Journal of Neurology, 2018, v. 265, n. 6, p. 1443, doi. 10.1007/s00415-018-8852-5
- By:
- Publication type:
- Article
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 5, p. 573, doi. 10.1093/hmg/ddh059
- By:
- Publication type:
- Article
Glutathione S-transferase omega-1 modifiesage-at-onset of Alzheimer disease and Parkinson disease.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 24, p. 3259, doi. 10.1093/hmg/ddg357
- By:
- Publication type:
- Article
Factors Associated With the Place of Death in Huntington Disease: Analysis of Enroll-HD.
- Published in:
- Journal of Palliative Medicine, 2023, v. 26, n. 7, p. 915, doi. 10.1089/jpm.2022.0143
- By:
- Publication type:
- Article
Death Anxiety in Huntington Disease: Longitudinal Heath-Related Quality-of-Life Outcomes.
- Published in:
- Journal of Palliative Medicine, 2023, v. 26, n. 7, p. 907, doi. 10.1089/jpm.2022.0160
- By:
- Publication type:
- Article
Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and machado-joseph disease.
- Published in:
- Annals of Neurology, 1996, v. 40, n. 2, p. 199, doi. 10.1002/ana.410400211
- By:
- Publication type:
- Article
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.
- Published in:
- Neurogenetics, 2013, v. 14, n. 3/4, p. 173, doi. 10.1007/s10048-013-0364-y
- By:
- Publication type:
- Article
A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.
- Published in:
- Neurogenetics, 2004, v. 5, n. 3, p. 157, doi. 10.1007/s10048-004-0186-z
- By:
- Publication type:
- Article
Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.
- Published in:
- Neurogenetics, 2004, v. 5, n. 2, p. 109, doi. 10.1007/s10048-004-0175-2
- By:
- Publication type:
- Article
Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?
- Published in:
- 2019
- By:
- Publication type:
- Letter
The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.
- Published in:
- Movement Disorders, 2015, v. 30, n. 2, p. 278, doi. 10.1002/mds.26065
- By:
- Publication type:
- Article
Challenges assessing clinical endpoints in early Huntington disease.
- Published in:
- Movement Disorders, 2010, v. 25, n. 15, p. 2595, doi. 10.1002/mds.23337
- By:
- Publication type:
- Article
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Participant-reported personal utility of genetic testing for Parkinson's disease and interest in clinical trial participation.
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00805-z
- By:
- Publication type:
- Article
Genome-wide significance for a modifier of age at neurological onset in Huntington's Disease at 6q23-24: the HD MAPS study.
- Published in:
- BMC Medical Genetics, 2006, v. 7, p. 71, doi. 10.1186/1471-2350-7-71
- By:
- Publication type:
- Article