A clinical case of neonatal diabetes caused by INS gene mutation
Neonatal diabetes mellitus (NDM) is a severe endocrine pathology diagnosed in children during the first months of life. It comprises rare (1:300 000–1:400 000 newborns) metabolic disorders with postnatal pancreatic β-cell dysfunction, manifested by hyperglycaemia and hypoinsulinae...
Guardado en:
Autores principales: | Rosa A. Atanesyan, Tatyana A. Uglova, Tatyana M. Vdovina, Leonid Ya. Klimov, Marina U. Kostanova, Victoriya A. Kuryaninova, Marina V. Stoyan, Lilit S. Alaverdyan, Svetlana V. Dolbnya |
---|---|
Formato: | article |
Lenguaje: | EN RU |
Publicado: |
Endocrinology Research Centre
2019
|
Materias: | |
Acceso en línea: | https://doaj.org/article/752e9da87603460985a3aaa39fa93caf |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Rabson-Mendenhall syndrome in a 13 y.o. child (clinical case)
por: Roza Arturovna Atanesyan, et al.
Publicado: (2015) -
Intraperitoneal insulin infusion: on the way to the artificial pancreas
por: Vladimir Aleksandrovich Karpel'ev, et al.
Publicado: (2015) -
Dose adjustment in insulin pump therapy: optimization of bolus calculator settings
por: Yury Ivanovich Filippov, et al.
Publicado: (2012) -
Overcoming marked insulin resistance in a patient with type 2 diabetes mellitus by means of insulin pumptherapy
por: Ekaterina Viktorovna Artemova, et al.
Publicado: (2012) -
Development and in silico validation of the PID-algorithm for the artificial pancreas with intraperitoneal insulin delivery
por: Vladimir A. Karpelyev, et al.
Publicado: (2018)