Exercise induced hypoglycaemic hyperinsulinism

Archives of Disease in Childhood

Volumn 84, Issue 3, 2001, Pages 254-257

  Meissner, T ^a   Otonkoski, T ^b   Feneberg, R ^a   Beinbrech, B ^a   Apostolidou, S ^a   Sipila I ^b   Schaefer, F ^a   Mayatepek, E ^a  

^a UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

^b UNIVERSITY OF HELSINKI   (Finland)

Author keywords

Congenital hyperinsulinism; Exercise; Hyperinsulinism; Hypoglycaemia

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; EXERCISE; FEMALE; GLUCOSE BLOOD LEVEL; HORMONAL REGULATION; HUMAN; HYPERINSULINISM; HYPOGLYCEMIA; INSULIN RELEASE; MALE; PRIORITY JOURNAL;

ADOLESCENT; CASE-CONTROL STUDIES; EXERCISE; EXERCISE TEST; FEMALE; HUMANS; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; MALE; SEIZURES; SYNCOPE;

EID: 0035088153     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/adc.84.3.254     Document Type: Article

References (9)

1. Nesidioblastosis of the pancreas: Definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemia
2. Persistent hyperinsulinemic hypoglycaemia of infancy: Molecular basis of a heterogeneous disease
3. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycaemia of infancy
4. Familial hyperinsulinism caused by an activating glucokinase mutation
5. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene
6. Synchronous fluctuations of blood insulin and lactate concentrations in humans
7. Hyperinsulinism: Molecular etiology of focal disease
8. Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia
9. Familial hyperinsulinism presenting in adults