Persistent hyperinsulinaemic hypoglycaemia of infancy: Therapy, clinical outcome and mutational analysis

European Journal of Pediatrics

Volumn 156, Issue 10, 1997, Pages 754-757

  Meissner, T ^a   Brune, W ^b   Mayatepek, E ^a  

^a UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

Author keywords

Mutational analysis; Nesidioblastosis; Pancreatectomy; Persistent hyperinsulinaemic hypoglycaemia of infancy; Sulphonylurea receptor

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; FEMALE; GENE MUTATION; GLUCOSE BLOOD LEVEL; HUMAN; HYPERINSULINEMIA; HYPOGLYCEMIA; INSULIN RELEASE; MALE; PANCREAS RESECTION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; ATP-BINDING CASSETTE TRANSPORTERS; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; FEMALE; HETEROZYGOTE DETECTION; HUMANS; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; INFANT, NEWBORN; MALE; PANCREAS; PANCREATECTOMY; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG; TREATMENT OUTCOME;

EID: 0030764203     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310050706     Document Type: Article

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