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1.
[Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(4): 413-418, 2023 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-36972934
2.
Entropy Confinement Promotes Hydrogenolysis Activity for Polyethylene Upcycling.
Angew Chem Int Ed Engl
; 62(47): e202313174, 2023 Nov 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-37799095
3.
A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report.
BMC Pediatr
; 21(1): 256, 2021 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34074259
4.
Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report.
BMC Pediatr
; 20(1): 315, 2020 06 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-32593294
5.
Clinical analysis and literature review of two paediatric cases of anti-IgLON5 antibody-related encephalitis.
Front Neurol
; 15: 1388970, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38765268
6.
Clinical and genetic analyses of APMR4 syndrome caused by novel biallelic LSS variants.
Front Neurosci
; 18: 1301865, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38800572
7.
Hydrogen Bubbles: Harmonizing Local Hydrogen Transfer for Efficient Plastic Hydro-Depolymerization.
ACS Nano
; 18(17): 11438-11448, 2024 Apr 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-38627232
8.
Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study.
Front Immunol
; 14: 1140872, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37153594
9.
Clinical characteristics of Chinese pediatric patients positive for anti-NMDAR and MOG antibodies: a case series.
Front Neurol
; 14: 1279211, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38249740
10.
Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients.
Front Neurol
; 14: 1310419, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38174099
11.
[Effects of electrode on epileptogenic focus potential and expressions of the beta subunit of ATP synthase in rats with penicillin-induced epilepsy].
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi
; 29(2): 287-90, 2012 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-22616176
12.
Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort Study.
Front Pediatr
; 10: 880693, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35874583
13.
MORC2 gene de novo mutation leads to Charcot-Marie-Tooth disease type 2Z: A pediatric case report and literature review.
Medicine (Baltimore)
; 100(37): e27208, 2021 Sep 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-34664855
14.
Self-assembled nanogels of luminescent thiolated silver nanoclusters and chitosan as bactericidal agent and bacterial sensor.
Mater Sci Eng C Mater Biol Appl
; 118: 111520, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-33255075
15.
CNKSR2 gene mutation leads to Houge type of X-linked syndromic mental retardation: A case report and review of literature.
Medicine (Baltimore)
; 100(23): e26093, 2021 Jun 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34114993
16.
Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation.
Front Pediatr
; 9: 801719, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34966709
17.
Revaluation of clopidogrel: let the data speak for themselves.
J Huazhong Univ Sci Technolog Med Sci
; 30(3): 299-306, 2010 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-20556571
18.
Mutant BCL11B in a Patient With a Neurodevelopmental Disorder and T-Cell Abnormalities.
Front Pediatr
; 8: 544894, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33194885
19.
Revaluation of Clopidogrel: Let the Data Speak for Themselves / 华中科技大学学报(医学)(英德文版)
Journal of Huazhong University of Science and Technology (Medical Sciences)
; (6): 299-306, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-349833
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