Hyperinsulinism in children;Hyperinsulinismes

Archives de Pediatrie

Volumn 8, Issue SUPPL. 2, 2001, Pages

  De Lonlay Debeney, P ^a   Fournet, J C ^a   Touati, G ^a   Robert, J J ^a   Junien, C ^a   Saudubray, J M ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; DIAZOXIDE; GLUCAGON; GLUCOSE; INSULIN; LEUCINE; SOMATOSTATIN;

CHILD; CLINICAL FEATURE; CONFERENCE PAPER; DIAGNOSTIC PROCEDURE; HEREDITY; HUMAN; HYPERINSULINISM; HYPOGLYCEMIA; PANCREAS RESECTION;

CHILD; HUMANS; HYPERINSULINISM; POTASSIUM CHANNELS;

EID: 0034888204     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (10)

1. Hyperinsulinism in infants and children
2. Clinical features of 52 neonates with hyperinsulinism
3. Neonatal hyperinsulinemic hypoglycemia: Heterogeneity of the syndrome and keys for differential diagnosis
4. Hyperinsulinism in children: Diagnosis value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases
5. B-cell proliferation and apoptosis in the developping normal human pancreas and in hyperinsulinism of infancy
6. Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism
7. Loss of the maternal chromosome 11p15 with reduction to homozygosity of a paternal mutation in the SUR gene results in hyperinsulinism of infancy with pancreatic focal adenomatous hyperplasia
8. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
9. Mutation of the pancreatic islet inward rectifier KIR6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
10. Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1