Detalhe da pesquisa
1.
International Genetic Testing and Counseling Practices for Parkinson's Disease.
Mov Disord
; 38(8): 1527-1535, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37310233
2.
Genetic Testing in Parkinson's Disease.
Mov Disord
; 38(8): 1384-1396, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37365908
3.
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease.
Ann Neurol
; 90(1): 76-88, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33938021
4.
Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism.
Mov Disord
; 37(11): 2217-2225, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36054306
5.
Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls.
Mov Disord
; 34(9): 1392-1398, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31348549
6.
Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism.
Mov Disord
; 38(4): 714-715, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37061880
7.
Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers.
Mov Disord
; 33(6): 966-973, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29603409
8.
Assessment of Glucocerebrosidase Enzyme Activity in Parkinson Disease Using Multiple Approaches.
Mov Disord
; 37(3): 655-656, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35106836
9.
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
Hum Mol Genet
; 23(17): 4693-702, 2014 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24842889
10.
Arm swing as a potential new prodromal marker of Parkinson's disease.
Mov Disord
; 31(10): 1527-1534, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27430880
11.
Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations.
Mov Disord
; 30(7): 904-8, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25952684
12.
Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.
Mov Disord
; 30(7): 981-6, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25809001
13.
Low-variance RNAs identify Parkinson's disease molecular signature in blood.
Mov Disord
; 30(6): 813-21, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25786808
14.
REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers.
Mov Disord
; 30(13): 1834-9, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26366513
15.
Interest in genetic testing in Ashkenazi Jewish Parkinson's disease patients and their unaffected relatives.
J Genet Couns
; 24(2): 238-46, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25127731
16.
Evidence for increased completed suicide in first-degree relatives of LRRK2 G2019S mutation Parkinson's disease.
J Neurol Neurosurg Psychiatry
; 90(7): 843-844, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30409888
17.
Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.
Mov Disord
; 29(6): 812-8, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24500857
18.
Deep Brain Stimulation in Isolated Dystonia With a GNAL Mutation.
Mov Disord
; 34(2): 301-303, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30536916
19.
LRRK2 G2019S variant is associated with transcriptional changes in Parkinson's disease human myeloid cells under proinflammatory environment.
bioRxiv
; 2024 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-38854101
20.
Increased substantia nigra echogenicity in LRRK2 family members without mutations.
Mov Disord
; 33(9): 1504-1505, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30145825