Detalhe da pesquisa
1.
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability.
Brain
; 146(4): 1496-1510, 2023 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36073231
2.
Cerebellar Volume and Disease Staging in Parkinson's Disease: An ENIGMA-PD Study.
Mov Disord
; 38(12): 2269-2281, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37964373
3.
The South African Parkinson's Disease Study Collection.
Mov Disord
; 37(1): 230-232, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34676912
4.
Movement of prion-like α-synuclein along the gut-brain axis in Parkinson's disease: A potential target of curcumin treatment.
Eur J Neurosci
; 54(2): 4695-4711, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34043864
5.
Availability of Therapies and Services for Parkinson's Disease in Africa: A Continent-Wide Survey.
Mov Disord
; 36(10): 2393-2407, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34080713
6.
Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patients.
BMC Med Genet
; 21(1): 23, 2020 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32019516
7.
Frequency of the LRRK2 G2019S mutation in South African patients with Parkinson's disease.
Neurogenetics
; 20(4): 215-218, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31493133
8.
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability.
Mov Disord
; 33(11): 1814-1819, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30398675
9.
The Gaps and Prospects of Movement Disorders Education and Research in Africa: A Continental Survey.
Mov Disord
; 38(2): 178-184, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36703239
10.
Using Eulerian video magnification to enhance detection of fasciculations in people with amyotrophic lateral sclerosis.
Muscle Nerve
; 56(6): 1063-1067, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28500626
11.
Copy Number Variation in Parkinson's Disease: An Update from Sub-Saharan Africa.
Mov Disord
; 36(10): 2442-2444, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34228376
12.
Mitochondrial impairment observed in fibroblasts from South African Parkinson's disease patients with parkin mutations.
Biochem Biophys Res Commun
; 447(2): 334-40, 2014 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24721425
13.
Screening of two indel polymorphisms in the 5'UTR of the DJ-1 gene in South African Parkinson's disease patients.
J Neural Transm (Vienna)
; 121(2): 135-8, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24052110
14.
Atypical Presentations of Huntington Disease-like 2 in South African Individuals.
Mov Disord Clin Pract
; 2024 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38725192
15.
Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.
Mov Disord
; 28(12): 1740-4, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23913756
16.
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and Human Immunodeficiency virus infection: dilemmas in diagnosis and management: a case series.
J Med Case Rep
; 17(1): 457, 2023 Oct 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37845760
17.
Alpha-synuclein-associated changes in PINK1-PRKN-mediated mitophagy are disease context dependent.
Brain Pathol
; 33(5): e13175, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37259617
18.
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.
PLoS One
; 18(10): e0292180, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37788254
19.
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.
Hum Mol Genet
; 19(10): 1998-2004, 2010 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20197411
20.
Neurological letter from Cape Town.
Pract Neurol
; 17(1): 74-76, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27888233