Detalhe da pesquisa
1.
Providing genetic testing and genetic counseling for Parkinson's disease to the community.
Genet Med
; 25(10): 100907, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37302021
2.
Genetic testing for Parkinson disease: current practice, knowledge, and attitudes among US and Canadian movement disorders specialists.
Genet Med
; 22(3): 574-580, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31680121
3.
Correction: Genetic testing for Parkinson disease: current practice, knowledge, and attitudes among US and Canadian movement disorders specialists.
Genet Med
; 22(2): 448, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31772350
4.
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder.
Am J Hum Genet
; 99(6): 1229-1244, 2016 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27817865
5.
Genetic counseling and testing for Huntington's disease: A historical review.
Am J Med Genet B Neuropsychiatr Genet
; 174(1): 75-92, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27174011
6.
National Randomized Controlled Trial of Virtual House Calls for People with Parkinson's Disease: Interest and Barriers.
Telemed J E Health
; 22(7): 590-8, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26886406
7.
Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.
Am J Hum Genet
; 90(3): 434-44, 2012 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22387017
8.
The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.
Mov Disord
; 30(2): 278-83, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25393808
9.
Experience, knowledge, and opinions about childhood genetic testing in Batten disease.
Mol Genet Metab
; 111(2): 197-202, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24246680
10.
Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?
Mov Disord
; 34(4): 584-585, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30788860
11.
Delivering Genetic Test Results for Parkinson Disease: A Qualitative Approach to Provider Experiences in the PD GENEration Study.
Neurol Clin Pract
; 14(2): e200282, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38486810
12.
Clinical Review of Juvenile Huntington's Disease.
J Huntingtons Dis
; 2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38669553
13.
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.
Neurogenetics
; 14(3-4): 173-9, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23644918
14.
Factors Associated With the Place of Death in Huntington Disease: Analysis of Enroll-HD.
J Palliat Med
; 26(7): 915-921, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36706436
15.
What we don't need to prove but need to do in multidisciplinary treatment and care in Huntington's disease: a position paper.
Orphanet J Rare Dis
; 18(1): 19, 2023 01 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36717864
16.
Advance Care Planning and Health-Related Quality of Life in Huntington Disease: Results from a Multicenter National Study.
Palliat Med Rep
; 4(1): 79-88, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36969738
17.
Death Anxiety in Huntington Disease: Longitudinal Heath-Related Quality-of-Life Outcomes.
J Palliat Med
; 26(7): 907-914, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36607769
18.
Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset.
Hum Genet
; 131(12): 1833-40, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22825315
19.
TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease.
Biochem Biophys Res Commun
; 424(3): 404-8, 2012 Aug 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22771793
20.
Therapy in Huntington's disease: where are we?
Curr Neurol Neurosci Rep
; 12(4): 359-66, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22544535