18 results on '"Gan, Siyi"'
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2. Post-traumatic Growth and Influencing Factors of Parents With Children With Duchenne Muscular Dystrophy: A Cross-sectional Survey Study
3. HCN1 pathogenic variants associated with childhood epilepsy in a cohort of Chinese patients
4. Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study
5. Differential Analysis of Metabolome in Gannan Navel Orange at Different Growth Levels
6. Clinical and genetic characteristics of Chinese Duchenne/Becker muscular dystrophy patients with small mutations
7. Untargeted metabolomics analysis based on HS-SPME-GC-MS and UPLC-Q-TOF/MS reveals the contribution of stem to the flavor of Cyclocarya paliurus herbal extract
8. Analysis of clinical phenotypic and genotypic spectra in 36 children patients with Epilepsy of Infancy with Migrating Focal Seizures
9. ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration
10. Multisystem Mitochondrial Disease Associated With a Mare m.10000G>A Mitochondrial tRNAGly (MT-TG) Variant
11. Krabbe Disease Associated With Mitochondrial Dysfunction in a Chinese Family
12. Epilepsy of Infancy With Migrating Focal Seizures (EIMFS): Expansion of Clinical Phenotypic And Genotypic Spectra
13. A pediatric case report and literature review of facioscapulohumeral muscular dystrophy type1
14. Malignant Migrating Partial Seizures of Infancy (MMPSI): Expansion of Clinical Phenotypic and Genotypic Spectra
15. Case Report: ISPD Gene Mutation Leads to Dystroglycanopathies: Genotypic Phenotype Analysis and Treatment Exploration
16. The Study of Genetic Susceptibility and Mitochondrial Dysfunction in Mesial Temporal Lobe Epilepsy
17. A correlation analysis between clinical manifestations, therapeutic strategies, and the prognosis of children with cryptococcal meningitis in China
18. AGRN Gene Mutation Leads to Congenital Myasthenia Syndromes: A Pediatric Case Report and Literature Review
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