Detalhe da pesquisa
1.
[Analysis of ALMS1 gene variants in seven patients with Alström syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(2): 112-116, 2021 Feb 10.
Artigo
em Zh
| MEDLINE | ID: mdl-33565060
2.
DEPDC5 protects CD8+ T cells from ferroptosis by limiting mTORC1-mediated purine catabolism.
Cell Discov
; 10(1): 53, 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38763950
3.
NOX, the main regulator in oxidative stress in experimental models of phenylketonuria?
J Pediatr Endocrinol Metab
; 26(7-8): 675-82, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23612646
4.
Sleep Disturbances in Chinese Children with Epilepsy: Associations with Behavioral Problems and Quality of Life.
Nat Sci Sleep
; 14: 1225-1236, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35814490
5.
MicroRNA-140-5p regulates the proliferation, apoptosis and inflammation of RA FLSs by repressing STAT3.
Exp Ther Med
; 21(2): 171, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33456538
6.
Genetic Diagnosis Spectrum and Multigenic Burden of Exome-Level Rare Variants in a Childhood Epilepsy Cohort.
Front Genet
; 12: 782419, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34992632
7.
[Value of Glasgow-Pittsburgh Coma Scale scoring in childhood coma].
Zhongguo Dang Dai Er Ke Za Zhi
; 10(5): 614-6, 2008 Oct.
Artigo
em Zh
| MEDLINE | ID: mdl-18947483
8.
Novel TSC1 and TSC2 gene mutations in Chinese patients with tuberous sclerosis complex.
Clin Neurol Neurosurg
; 154: 104-108, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28178598
9.
The oxidative molecular regulation mechanism of NOX in children with phenylketonuria.
Int J Dev Neurosci
; 38: 178-83, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25256805
10.
[Neonatal lupus syndromes].
Zhongguo Dang Dai Er Ke Za Zhi
; 9(6): 622-4, 2007 Dec.
Artigo
em Zh
| MEDLINE | ID: mdl-18082061