Found: 6
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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
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- 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
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- Publication type:
- journal article
A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report.
- Published in:
- 2021
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- Publication type:
- journal article
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
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- Publication type:
- Article
Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study.
- Published in:
- Italian Journal of Pediatrics, 2023, v. 49, n. 1, p. 1, doi. 10.1186/s13052-023-01483-y
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- Publication type:
- Article
Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations.
- Published in:
- Frontiers in Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnins.2022.1076183
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- Publication type:
- Article