Detalhe da pesquisa
1.
Optimization strategy for the early timing of bronchoalveolar lavage treatment for children with severe mycoplasma pneumoniae pneumonia.
BMC Infect Dis
; 23(1): 661, 2023 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37798699
2.
Characteristics of in-hospital mortality of congenital heart disease (CHD) after surgical treatment in children from 2005 to 2017: a single-center experience.
BMC Pediatr
; 21(1): 521, 2021 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34814864
3.
Empagliflozin in children with glycogen storage disease-associated inflammatory bowel disease: a prospective, single-arm, open-label clinical trial.
Sci Rep
; 14(1): 8630, 2024 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38622211
4.
Long-term risks of respiratory diseases in patients infected with SARS-CoV-2: a longitudinal, population-based cohort study.
EClinicalMedicine
; 69: 102500, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38389713
5.
Timing of bronchoscopy and application of scoring tools in children with severe pneumonia.
Ital J Pediatr
; 49(1): 44, 2023 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37024936
6.
Alagille syndrome associated with total anomalous pulmonary venous connection and severe xanthomas: A case report.
World J Clin Cases
; 10(25): 8932-8938, 2022 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36157644
7.
A Polyhydroxyalkanoates-Based Carrier Platform of Bioactive Substances for Therapeutic Applications.
Front Bioeng Biotechnol
; 9: 798724, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35071207
8.
Molecular epidemiologic study of citrin deficiency by screening for four reported pathogenic SLC25A13 variants in the Shaanxi and Guangdong provinces, China.
Transl Pediatr
; 10(6): 1658-1667, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34295780
9.
Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein-Taybi syndrome.
Orphanet J Rare Dis
; 15(1): 101, 2020 04 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32321550
10.
SLC25A13 cDNA cloning analysis using peripheral blood lymphocytes facilitates the identification of a large deletion mutation: Molecular diagnosis of an infant with neonatal intrahepatic cholestasis caused by citrin deficiency.
Mol Med Rep
; 14(6): 5189-5194, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27779681
11.
Identification of a Large SLC25A13 Deletion via Sophisticated Molecular Analyses Using Peripheral Blood Lymphocytes in an Infant with Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency (NICCD): A Clinical and Molecular Study.
Biomed Res Int
; 2016: 4124263, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27127784
12.
Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution.
Sci Rep
; 6: 29732, 2016 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27405544
13.
Inspissated bile syndrome in an infant with citrin deficiency and congenital anomalies of the biliary tract and esophagus: identification and pathogenicity analysis of a novel SLC25A13 mutation with incomplete penetrance.
Int J Mol Med
; 34(5): 1241-8, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25216257
14.
Clinical, molecular and functional investigation on an infant with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).
PLoS One
; 9(2): e89267, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24586645