Detalhe da pesquisa
1.
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Kidney Int
; 105(4): 844-864, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38154558
2.
In-depth mutational analyses of colorectal neuroendocrine carcinomas with adenoma or adenocarcinoma components.
Mod Pathol
; 30(1): 95-103, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27586204
3.
Extracorporeal light-chain elimination in myeloma with simple medium cutoff membrane hemodialysis: a retrospective cohort study.
Front Oncol
; 13: 1193504, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37746285
4.
The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience.
Front Med (Lausanne)
; 9: 957733, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36117978