Molecular mechanisms of neonatal hyperinsulinism.

Molecular mechanisms of neonatal hyperinsulinism.

Item
http://www.wikidata.org/entity/Q36604826
Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism.Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescuePersistent hyperinsulinemic hypoglycemia of infancy: a clinical and pathological study of 19 cases in a single institutionNovel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescenceDiagnosis and management of hyperinsulinaemic hypoglycaemia of infancy.Mutations in SLC2A2 gene reveal hGLUT2 function in pancreatic β cell development.Knowledge gaps and research needs for understanding and treating neonatal hypoglycemia: workshop report from Eunice Kennedy Shriver National Institute of Child Health and Human Development.A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infant.Remission of congenital hyperinsulinism following conservative treatment: an exploratory study in patients with KATP channel mutations.
P2860

Molecular mechanisms of neonatal hyperinsulinism.

Item
http://www.wikidata.org/entity/Q36604826
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Molecular mechanisms of neonatal hyperinsulinism.
@ast
Molecular mechanisms of neonatal hyperinsulinism.
@en
type
label
Molecular mechanisms of neonatal hyperinsulinism.
@ast
Molecular mechanisms of neonatal hyperinsulinism.
@en
prefLabel
Molecular mechanisms of neonatal hyperinsulinism.
@ast
Molecular mechanisms of neonatal hyperinsulinism.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P356
P1433
P1476
Molecular mechanisms of neonatal hyperinsulinism.
@en
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698