Latest papers

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.

Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation.

Cotrimoxazole induced mixed type II cryoglobulinemia

Gene duplications resulting in over expression of glucokinase are not a common cause of hypoglycaemia of infancy in humans.

Adult hyperinsulinaemic hypoglycaemia caused by coexisting nesidioblastosis and insulinoma

Glucose intolerance and diabetes are observed in the long-term follow-up of nonpancreatectomized patients with persistent hyperinsulinemic hypoglycemia of infancy due to mutations in the ABCC8 gene.

Long-term follow-up of patients with congenital hyperinsulinism in Austria.

Destabilization of ATP-sensitive potassium channel activity by novel KCNJ11 mutations identified in congenital hyperinsulinism.

Evaluation of [18F]fluoro-L-DOPA positron emission tomography-computed tomography for surgery in focal congenital hyperinsulinism.

Hyperinsulinism in infancy and childhood: when an insulin level is not always enough.

K(ATP) channel pharmacogenomics: from bench to bedside.

Congenital central hypoventilation syndrome with hyperinsulinism in a preterm infant.

Mutations in UCP2 in congenital hyperinsulinism reveal a role for regulation of insulin secretion.

Long-term non-surgical therapy of severe persistent congenital hyperinsulinism with glucagon.

Alanine in HI: a silent mutation cries out!

Diagnosis and management of hyperinsulinaemic hypoglycaemia of infancy.

Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy.

Octreotide-induced severe paradoxical hyperglycemia and bradycardia during subtotal pancreatectomy for congenital hyperinsulinism in an infant.

The laparoscopic approach toward hyperinsulinism in children

Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism.