Detalhe da pesquisa
1.
Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease.
Proc Natl Acad Sci U S A
; 120(16): e2214997120, 2023 04 18.
Artigo
Inglês
| MEDLINE | ID: mdl-37043537
2.
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease.
Proc Natl Acad Sci U S A
; 121(12): e2319578121, 2024 Mar 19.
Artigo
Inglês
| MEDLINE | ID: mdl-38466853
3.
Novel compound heterozygous mutations in GPT2 linked to microcephaly, and intellectual developmental disability with or without spastic paraplegia.
Am J Med Genet A
; 176(2): 421-425, 2018 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29226631
4.
Illness Perception and the Impact of a Definitive Diagnosis on Women With Ischemia and No Obstructive Coronary Artery Disease: A Qualitative Study.
Circ Cardiovasc Qual Outcomes
; 16(8): 521-529, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37476997
5.
Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM.
Turk Arch Pediatr
; 57(5): 521-525, 2022 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-35950747
6.
Strengthening Public Health Scholarship in Sudan: The Role of Leadership and Mentorship Development.
Am J Trop Med Hyg
; 107(6): 1323-1330, 2022 12 14.
Artigo
Inglês
| MEDLINE | ID: mdl-36343591
7.
Strengthening the Mentorship and Leadership Capacity of HIV/AIDS and Tuberculosis Researchers in South Africa.
Am J Trop Med Hyg
; 105(5): 1317-1325, 2021 08 16.
Artigo
Inglês
| MEDLINE | ID: mdl-34398822
8.
PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans.
Nat Med
; 27(12): 2165-2175, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34887573