Found: 8
Select item for more details and to access through your institution.
Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1140872
- By:
- Publication type:
- Article
Entropy Confinement Promotes Hydrogenolysis Activity for Polyethylene Upcycling.
- Published in:
- Angewandte Chemie, 2023, v. 135, n. 47, p. 1, doi. 10.1002/ange.202313174
- By:
- Publication type:
- Article
Clinical and genetic analyses of APMR4 syndrome caused by novel biallelic LSS variants.
- Published in:
- Frontiers in Neuroscience, 2024, p. 1, doi. 10.3389/fnins.2024.1301865
- By:
- Publication type:
- Article
Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Entropy Confinement Promotes Hydrogenolysis Activity for Polyethylene Upcycling.
- Published in:
- Angewandte Chemie International Edition, 2023, v. 62, n. 47, p. 1, doi. 10.1002/anie.202313174
- By:
- Publication type:
- Article
Clinical analysis and literature review of two paediatric cases of anti-IgLON5 antibody-related encephalitis.
- Published in:
- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1388970
- By:
- Publication type:
- Article
Clinical characteristics of Chinese pediatric patients positive for anti-NMDAR and MOG antibodies: a case series.
- Published in:
- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2023.1279211
- By:
- Publication type:
- Article
A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report.
- Published in:
- 2021
- By:
- Publication type:
- journal article