Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Genetic characteristics and long-term follow-up of 11 patients with congenital hyperinsulinism followed in a single center.
|
27682711 |
2016 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
CausalMutation
|
disease |
CLINVAR |
Clinical and genetic evaluation of patients with KATP channel mutations from the German registry for congenital hyperinsulinism.
|
24401662 |
2014 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Occurrence of giant focal forms of congenital hyperinsulinism with incorrect visualization by (18) F DOPA-PET/CT scanning.
|
24750227 |
2014 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
CausalMutation
|
disease |
CLINVAR |
Congenital hyperinsulinism.
|
25323548 |
2014 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia.
|
25117148 |
2014 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations.
|
25201519 |
2014 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Efficacy and safety of long-term, continuous subcutaneous octreotide infusion for patients with different subtypes of KATP-channel hyperinsulinism.
|
23067144 |
2013 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.
|
23345197 |
2013 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Genetic analysis of Italian patients with congenital hyperinsulinism of infancy.
|
23652837 |
2013 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
CausalMutation
|
disease |
CLINVAR |
Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.
|
23275527 |
2013 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.
|
23275527 |
2013 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
CausalMutation
|
disease |
CLINVAR |
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.
|
23345197 |
2013 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
GLP-1 receptor antagonist exendin-(9-39) elevates fasting blood glucose levels in congenital hyperinsulinism owing to inactivating mutations in the ATP-sensitive K+ channel.
|
22855730 |
2012 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
A universally conserved residue in the SUR1 subunit of the KATP channel is essential for translating nucleotide binding at SUR1 into channel opening.
|
22802590 |
2012 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism.
|
21378087 |
2011 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
CausalMutation
|
disease |
CLINVAR |
Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.
|
20943781 |
2011 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Familial focal congenital hyperinsulinism.
|
20943779 |
2011 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
In vitro recovery of ATP-sensitive potassium channels in β-cells from patients with congenital hyperinsulinism of infancy.
|
21411514 |
2011 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism.
|
21422196 |
2011 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism.
|
20685672 |
2010 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Functional hot spots in human ATP-binding cassette transporter nucleotide binding domains.
|
20799350 |
2010 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
CausalMutation
|
disease |
CLINVAR |
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism.
|
20685672 |
2010 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy.
|
19475716 |
2009 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism.
|
18767144 |
2009 |
Hyperinsulinemic hypoglycemia, familial, 2
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
Evaluation of [18F]fluoro-L-DOPA positron emission tomography-computed tomography for surgery in focal congenital hyperinsulinism.
|
18073294 |
2008 |