Cargando…
Correspondence to ‘Neonatal hypoglycaemia due to ABCC8 gene mutation’
Autor principal: | Maralihalli, Mahesh |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793952/ https://www.ncbi.nlm.nih.gov/pubmed/35136748 http://dx.doi.org/10.4103/ijem.ijem_312_21 |
Ejemplares similares
-
Neonatal Hypoglycaemia due to ABCC8 Gene Mutation
por: Kumar, Ashok, et al.
Publicado: (2020) -
Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations
por: Kapoor, R. R., et al.
Publicado: (2011) -
Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemia
por: Flanagan, SE, et al.
Publicado: (2011) -
A case of transient neonatal diabetes due to a novel mutation in ABCC8
por: Takagi, Masaki, et al.
Publicado: (2016) -
Partial diazoxide responsiveness in a neonate with hyperinsulinism due to homozygous ABCC8 mutation
por: Kiff, Sarah, et al.
Publicado: (2019)