Detalhe da pesquisa
1.
A case report of classic galactosemia with a GALT gene variant and a literature review.
BMC Pediatr
; 24(1): 352, 2024 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38778342
2.
[A multi-center epidemiological study on pneumococcal meningitis in children from 2019 to 2020]. / 20192020å¹´160ä¾å¿ç«¥èºçé¾çèèèç临åºæµè¡ç å¦å¤ä¸å¿ç 究.
Zhongguo Dang Dai Er Ke Za Zhi
; 26(2): 131-138, 2024 Feb 15.
Artigo
em Chinês
| MEDLINE | ID: mdl-38436309
3.
Bloody Diarrhea Caused by Intestinal Myiasis in an Infant: A Case Report and Review of Pediatric Literature.
J Trop Pediatr
; 67(3)2021 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32756975
4.
Effects of Zinc Combined with Probiotics on Antibiotic-associated Diarrhea Secondary to Childhood Pneumonia.
J Trop Pediatr
; 65(5): 421-426, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30521044
5.
Rare LPL gene missense mutation in an infant with hypertriglyceridemia.
J Clin Lab Anal
; 32(6): e22414, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29479812
6.
Taurine Regulates the Expression of Interleukin -17/10 and Intestinal Flora and Protects the Liver and Intestinal Mucosa in a Nonalcoholic Fatty Liver Disease Rat Model.
Diabetes Metab Syndr Obes
; 17: 675-689, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38352234
7.
Determination of the median lethal dose of zinc gluconate in mice and safety evaluation.
BMC Pharmacol Toxicol
; 25(1): 15, 2024 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38317260
8.
[Effects of ursodeoxycholic acid on mRNA expression of MDR3 and FXR in infants with cholestatic hepatitis].
Zhongguo Dang Dai Er Ke Za Zhi
; 15(9): 756-8, 2013 Sep.
Artigo
em Chinês
| MEDLINE | ID: mdl-24034919
9.
Screening for Wilson's disease in acute liver failure: A new scoring system in children.
Front Pediatr
; 10: 1003887, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36210929
10.
A simple noninvasive model to predict significant fibrosis in children with chronic hepatitis B.
Medicine (Baltimore)
; 100(25): e26462, 2021 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34160448
11.
Congenital disorder of glycosylation caused by mutation of ATP6AP1 gene (c.1036G>A) in a Chinese infant: A case report.
World J Clin Cases
; 9(26): 7876-7885, 2021 Sep 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34621841
12.
Antibiotic Use Among Hospitalized Children and Neonates in China: Results From Quarterly Point Prevalence Surveys in 2019.
Front Pharmacol
; 12: 601561, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33854430
13.
[NF-κB levels in the liver of young rats with endotoxemic liver injury].
Zhongguo Dang Dai Er Ke Za Zhi
; 12(10): 804-8, 2010 Oct.
Artigo
em Chinês
| MEDLINE | ID: mdl-20959047
14.
[Relationship between gene polymorphisms in MMP-9 and Helicobacter pylori-related upper gastrointestinal disease in children].
Zhongguo Dang Dai Er Ke Za Zhi
; 12(4): 262-6, 2010 Apr.
Artigo
em Chinês
| MEDLINE | ID: mdl-20416216
15.
A New Compound Heterozygous Mutation Of BSCL2 In A Chinese Zhuang Ethnic Family With Congenital Generalized Lipodystrophy.
Diabetes Metab Syndr Obes
; 12: 2583-2587, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31824185
16.
Congenital Sodium Diarrhea Caused by a Novel Spontaneous Mutation in the GUCY2C Gene.
Indian J Pediatr
; 90(3): 304, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36598634
17.
Detection of T lymphocyte subsets of children with Helicobacter pylori infection.
World J Gastroenterol
; 11(18): 2827-9, 2005 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-15884132
18.
A novel heterozygous NR1H4 termination codon mutation in idiopathic infantile cholestasis.
World J Pediatr
; 8(1): 67-71, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21633855
19.
Multidrug resistance protein 3 R652G may reduce susceptibility to idiopathic infant cholestasis.
World J Gastroenterol
; 15(46): 5855-8, 2009 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-19998509
20.
[Association of HLA-DQA1 loci with Helicobacter pylori infection in children of Guangxi Zhuang, Mulam nationalities, China and central Jing nationality, Vietnam].
Zhonghua Er Ke Za Zhi
; 42(8): 577-80, 2004 Aug.
Artigo
em Chinês
| MEDLINE | ID: mdl-15347442