Detalhe da pesquisa
1.
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export.
Acta Neuropathol
; 139(6): 1001-1024, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32172343
2.
Reply: ATP10B variants in Parkinson's disease-a large cohort study in Chinese mainland population.
Acta Neuropathol
; 141(5): 807-808, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33599815
3.
Reply: ATP10B and the risk for Parkinson's disease.
Acta Neuropathol
; 140(3): 403-404, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32542503
4.
Reply: Segregation of ATP10B variants in families with autosomal recessive Parkinsonism.
Acta Neuropathol
; 140(5): 787-789, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32892228
5.
Less cognitive and neurological deficits in schizophrenia patients carrying risk variant in ZNF804A.
Neuropsychobiology
; 66(3): 158-66, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22948380
6.
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
Acta Neuropathol Commun
; 9(1): 25, 2021 02 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33579389
7.
Genetic perspective on the synergistic connection between vesicular transport, lysosomal and mitochondrial pathways associated with Parkinson's disease pathogenesis.
Acta Neuropathol Commun
; 8(1): 63, 2020 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32375870
8.
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.
Neurology
; 83(21): 1906-13, 2014 Nov 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25326098