Detalhe da pesquisa
1.
Maternal secretin ameliorates obesity by promoting white adipose tissue browning in offspring.
EMBO Rep
; 23(7): e54132, 2022 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35652247
2.
PIGW-related glycosylphosphatidylinositol deficiency: A case report and literature review.
Neurol Sci
; 45(5): 2253-2260, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38055078
3.
Spinal muscular atrophy with hypoplasia of the corpus callosum: a case report.
BMC Neurol
; 23(1): 77, 2023 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36803361
4.
Gene therapeutic strategies and relevant clinical trials in neuromuscular disorder in China.
Gene Ther
; 27(7-8): 321-328, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32591735
5.
Comprehensive profile and natural history of pediatric patients with spinal muscular atrophy: A large retrospective study from China.
Front Neurol
; 13: 1038012, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36605788
6.
Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study.
Mitochondrion
; 62: 139-150, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34800692
7.
Clinical and Genetic Characteristics of Mitochondrial Encephalopathy Due to FOXRED1 Mutations: Two Chinese Case Reports and a Review of the Literature.
Front Neurol
; 12: 633397, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33613441
8.
Myotonia Congenita: Clinical Characteristic and Mutation Spectrum of CLCN1 in Chinese Patients.
Front Pediatr
; 9: 759505, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34790634
9.
Clinical Profile and Outcome of Pediatric Mitochondrial Myopathy in China.
Front Neurol
; 11: 1000, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33013660
10.
Clinical and molecular characterization of pediatric mitochondrial disorders in south of China.
Eur J Med Genet
; 63(8): 103898, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32348839
11.
Triazol: a privileged scaffold for proteolysis targeting chimeras.
Future Med Chem
; 11(22): 2919-2973, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31702389
12.
Concise synthesis of 2-methoxyestradiol from 17ß-estradiol through the C(sp2)-H hydroxylation.
Steroids
; 146: 99-103, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30951759
13.
A comprehensive database of Duchenne and Becker muscular dystrophy patients (0-18 years old) in East China.
Orphanet J Rare Dis
; 10: 5, 2015 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-25612904