Cargando…
High FGF‐21 level in a cohort of 22 patients with Dravet Syndrome—Possible relationship with the disease outcomes
OBJECTIVE: Dravet syndrome (DS) is a severe and intractable form of epilepsy with prolonged seizures which may evolve to other seizure types and associated with mild‐to‐severe intellectual disabilities. Fibroblast growth factor 21 (FGF‐21) is a stress hormone mediating metabolic and oxidative stress...
Autores principales: | Kwong, Anna Ka‐Yee, Wong, Virginia Chun‐Nei, Wong, Sheila Suet‐Na, Chu, Vanessa Loi‐Yan, Koene, Saskia, Smeitink, Jan, Fung, Cheuk‐Wing |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633467/ https://www.ncbi.nlm.nih.gov/pubmed/34379890 http://dx.doi.org/10.1002/epi4.12534 |
Ejemplares similares
-
Identification of SCN1A and PCDH19 Mutations in Chinese Children with Dravet Syndrome
por: Kwong, Anna Ka-Yee, et al.
Publicado: (2012) -
Gene panel analysis for nonsyndromic cryptogenic neonatal/infantile epileptic encephalopathy
por: Fung, Cheuk‐Wing, et al.
Publicado: (2017) -
Human d‐lactate dehydrogenase deficiency by LDHD mutation in a patient with neurological manifestations and mitochondrial complex IV deficiency
por: Kwong, Anna Ka‐Yee, et al.
Publicado: (2021) -
Analysis of Mutations in 7 Genes Associated with Neuronal Excitability and Synaptic Transmission in a Cohort of Children with Non-Syndromic Infantile Epileptic Encephalopathy
por: Kwong, Anna Ka-Yee, et al.
Publicado: (2015) -
Mitochondrial disorders in children: toward development of small‐molecule treatment strategies
por: Koopman, Werner JH, et al.
Publicado: (2016)