Detalhe da pesquisa
1.
A novel compound heterozygous EPM2A mutation in a Chinese boy with Lafora disease.
Neurol Sci
; 41(8): 2267-2270, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32342326
2.
The genotypic and phenotypic spectrum of PARS2-related infantile-onset encephalopathy.
J Hum Genet
; 63(9): 971-980, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29915213
3.
Serratia marcescens LYGN1 Reforms the Rhizosphere Microbial Community and Promotes Cucumber and Pepper Growth in Plug Seedling Cultivation.
Plants (Basel)
; 13(5)2024 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38475438
4.
Two patients with TNK2 mutations and late onset infantile spasm.
Ann Neurol
; 81(1): 161, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27977884
5.
Study on the established customized limits for the daily quality assurance procedure.
J Radiat Res
; 63(1): 128-136, 2022 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34734293
6.
Serum Visinin-Like Protein 1 Is a Better Biomarker Than Neuron-Specific Enolase for Seizure-Induced Neuronal Injury: A Prospective and Observational Study.
Front Neurol
; 11: 567587, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33071949
7.
STAT4: an immunoregulator contributing to diverse human diseases.
Int J Biol Sci
; 16(9): 1575-1585, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32226303
8.
A missense variant in complement factor B (CFB) is a potential predictor of 24-week off-treatment response to PegIFNα therapy in Chinese HBeAg-positive chronic hepatitis B patients.
Aliment Pharmacol Ther
; 51(4): 469-478, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31943297