Detalhe da pesquisa
1.
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
Nephrology (Carlton)
; 21(9): 753-7, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26560236
2.
Panoramic snapshot of serum soluble mediator interplay in pregnant women with convalescent COVID-19: an exploratory study.
Front Immunol
; 14: 1176898, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37122732
3.
Official Position of the Brazilian Association of Bone Assessment and Metabolism (ABRASSO) on the evaluation of body composition by densitometry-part II (clinical aspects): interpretation, reporting, and special situations.
Adv Rheumatol
; 62(1): 11, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35365246
4.
Selenoprotein-related disease in a young girl caused by nonsense mutations in the SBP2 gene.
J Clin Endocrinol Metab
; 95(8): 4066-71, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20501692