Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia

Annales d'Endocrinologie

Volumn 59, Issue 6, 1998, Pages 485-491

  Fournet, J C ^a,b   Verkarre, V ^a,b   De Lonlay, P ^a,b   Rahier, J ^c   Brunelle, F ^b   Robert, J J ^b   Nihoul Fekete C ^a   Saudubray, J M ^b   Junien, C ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b Department of Pathology ^*

^c CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

Author keywords

Beckwith Wiedermann; Imprinting; K+ ATP channel; Loss of allele sur 1 gene; Neonatal hypoglycemia; Persistent hyperinsulinism

Indexed keywords

ADENOSINE TRIPHOSPHATE; DIAZOXIDE; DNA; GLUCOKINASE; GLUCOSE; GLUTAMATE DEHYDROGENASE; INSULIN; POTASSIUM; SOMATOSTATIN; SULFONYLUREA RECEPTOR;

ADENOMA; ARTICLE; B LYMPHOCYTE; BECKWITH WIEDEMANN SYNDROME; CELL PROLIFERATION; CLINICAL ARTICLE; DIABETES MELLITUS; FOLLOW UP; GENE LOSS; GENE MUTATION; GENETIC ANALYSIS; HEMIZYGOSITY; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; HYPERINSULINISM; HYPOGLYCEMIA; INSULIN RELEASE; NEWBORN; NEWBORN DISEASE; PANCREAS ISLET CELL HYPERPLASIA; PANCREAS RESECTION; RECEPTOR GENE; RECESSIVE INHERITANCE; UNIPARENTAL DISOMY;

ADENOMA, ISLET CELL; ATP-BINDING CASSETTE TRANSPORTERS; CHROMOSOMES, HUMAN, PAIR 11; DIAZOXIDE; DRUG RESISTANCE; GENOMIC IMPRINTING; HUMANS; HYPERINSULINISM; HYPERPLASIA; HYPOGLYCEMIA; INFANT, NEWBORN; ISLETS OF LANGERHANS; MUTATION; PANCREATECTOMY; PANCREATIC NEOPLASMS; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG;

EID: 0032447019     PISSN: 00034266     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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