Detalhe da pesquisa
1.
Neuromuscular disease genetics in under-represented populations: increasing data diversity.
Brain
; 146(12): 5098-5109, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37516995
2.
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological Diseases.
Ann Neurol
; 89(6): 1240-1247, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33704825
3.
Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia.
J Neurol Neurosurg Psychiatry
; 88(8): 681-687, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28572275
4.
Vocation and avocation: leisure activities correlate with professional engagement, but not burnout, in a cross-sectional survey of UK doctors.
BMC Med
; 9: 100, 2011 Aug 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-21878123
5.
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease.
Neurobiol Aging
; 97: 148.e17-148.e24, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32873436
6.
Leucine rich repeat kinase 2 (LRRK2) GLY2019SER mutation is absent in a second cohort of Nigerian Africans with Parkinson disease.
PLoS One
; 13(12): e0207984, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30507963