Cargando…
The molecular mechanisms, diagnosis and management of congenital hyperinsulinism
Congenital hyperinsulinism (CHI) is the result of unregulated insulin secretion from the pancreatic β-cells leading to severe hypoglycaemia. In these patients it is important to make an accurate diagnosis and initiate the appropriate management so as to avoid hypoglycemic episodes and prevent the po...
Autores principales: | Senniappan, Senthil, Arya, Ved Bhushan, Hussain, Khalid |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659902/ https://www.ncbi.nlm.nih.gov/pubmed/23776849 http://dx.doi.org/10.4103/2230-8210.107822 |
Ejemplares similares
-
Pancreatic Endocrine and Exocrine Function in Children following Near-Total Pancreatectomy for Diffuse Congenital Hyperinsulinism
por: Arya, Ved Bhushan, et al.
Publicado: (2014) -
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism
por: Kapoor, Ritika R, et al.
Publicado: (2013) -
Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapy
por: Arya, Ved Bhushan, et al.
Publicado: (2014) -
Congenital Hyperinsulinism: Diagnosis and Treatment Update
por: Demirbilek, Hüseyin, et al.
Publicado: (2017) -
The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism
por: Galcheva, Sonya, et al.
Publicado: (2019)