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Hyperinsulinemic Hypoglycemia - The Molecular MechanismsHyperinsulinemic Hypoglycemia in Infancy: Current Concepts in Diagnosis and ManagementThe Diagnosis and Management of Hyperinsulinaemic HypoglycaemiaMultidomain integration in the structure of the HNF-4α nuclear receptor complexClinical and molecular data from 61 Brazilian cases of Congenital Hyperinsulinemic Hypoglycemia.Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations.[Hyperinsulinemic hypoglycemia of the infancy: analysis of clinical data from a Brazilian sample].Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigreesDrug-induced hepatitis following use of octreotide for long-term treatment of congenital hyperinsulinism.ABCC8 R1420H Loss-of-Function Variant in a Southwest American Indian Community: Association With Increased Birth Weight and Doubled Risk of Type 2 Diabetes.Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.Hypoglycaemia following diabetes remission in patients with 6q24 methylation defects: expanding the clinical phenotype.The management of hypertensive emergencies in children after stem cell transplantation.Current understanding of K ATP channels in neonatal diseases: focus on insulin secretion disorders.Occurrence of giant focal forms of congenital hyperinsulinism with incorrect visualization by (18) F DOPA-PET/CT scanning.Congenital hyperinsulinism: Role of fluorine-18L-3, 4 hydroxyphenylalanine positron emission tomography scanning.Recognition, assessment and management of hypoglycaemia in childhood.Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.An Egyptian case of congenital hyperinsulinism of infancy due to a novel mutation in KCNJ11 encoding Kir6.2 and response to octreotide.Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology.A combination of nifedipine and octreotide treatment in an hyperinsulinemic hypoglycemic infant.Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational ageInvestigation and management of congenital hyperinsulinism.A novel mutation in ABCC8 gene in a newborn with congenital hyperinsulinism -a case report.Congenital Hyperinsulinism: Diagnosis and Treatment Update.The evolving course of HNF4A hyperinsulinaemic hypoglycaemia--a case series.Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives.Population Pharmacokinetics of Diazoxide in Children with Hyperinsulinemic Hypoglycemia.Neonatal Glycemic Status of Infants of Diabetic Mothers in a Tertiary Care HospitalHeterozygous ABCC8 mutations are a cause of MODYHyperinsulinism-hyperammonemia syndrome in an infant with seizures
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 04 February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Hyperinsulinaemic hypoglycaemia.
@en
Hyperinsulinaemic hypoglycaemia.
@nl
type
label
Hyperinsulinaemic hypoglycaemia.
@en
Hyperinsulinaemic hypoglycaemia.
@nl
prefLabel
Hyperinsulinaemic hypoglycaemia.
@en
Hyperinsulinaemic hypoglycaemia.
@nl
P2093
P356
P1476
Hyperinsulinaemic hypoglycaemia
@en
P2093
P304
P356
10.1136/ADC.2008.148171
P407
P577
2009-02-04T00:00:00Z