Detalhe da pesquisa
1.
Common variation of the NSD1 gene is associated with susceptibility to Hirschsprung's disease in Chinese Han population.
Pediatr Res
; 89(3): 694-700, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32380506
2.
[Catheter directed thrombolysis for early left lower extremity deep venous thrombosis without vena cava filters protection].
Zhonghua Wai Ke Za Zhi
; 50(1): 15-8, 2012 Jan 01.
Artigo
Chinês
| MEDLINE | ID: mdl-22490283
3.
Evaluation Value and Clinical Significance of Cardiac Troponin Level and Pediatric Sequential Organ Failure Score in the Definition of Sepsis 3.0 in Critically Ill Children.
Comput Math Methods Med
; 2022: 9492178, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35983521
4.
Association Analysis of Variants of DSCAM and BACE2 With Hirschsprung Disease Susceptibility in Han Chinese and Functional Evaluation in Zebrafish.
Front Cell Dev Biol
; 9: 641152, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34136475
5.
Rapid detection of human heart-type fatty acid-binding protein in human plasma and blood using a colloidal gold-based lateral flow immunoassay.
Exp Ther Med
; 22(5): 1238, 2021 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-34539834
6.
Association of common variation in ADD3 and GPC1 with biliary atresia susceptibility.
Aging (Albany NY)
; 12(8): 7163-7182, 2020 04 21.
Artigo
Inglês
| MEDLINE | ID: mdl-32315284
7.
Association of Variants in PLD1, 3p24.1, and 10q11.21 Regions With Hirschsprung's Disease in Han Chinese Population.
Front Genet
; 11: 738, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32765588