Detalhe da pesquisa
1.
Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5.
Mov Disord
; 38(12): 2217-2229, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37752895
2.
Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48).
J Biomed Sci
; 28(1): 65, 2021 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34565360
3.
Autocrine CCL3 and CCL4 induced by the oncoprotein LMP1 promote Epstein-Barr virus-triggered B cell proliferation.
J Virol
; 87(16): 9041-52, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23760235
4.
A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration.
Parkinsonism Relat Disord
; 109: 105353, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36863113
5.
Evaluation of Transplacental Antibody Transfer in SARS-CoV-2-Immunized Pregnant Women.
Vaccines (Basel)
; 10(1)2022 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35062762
6.
Clinical Evaluation of a Self-Testing Kit for Vaginal Infection Diagnosis.
J Healthc Eng
; 2021: 4948954, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34394891
7.
Stress-induced p53 drives BAG5 cochaperone expression to control α-synuclein aggregation in Parkinson's disease.
Aging (Albany NY)
; 12(20): 20702-20727, 2020 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33085644