Histopathology of congenital hyperinsulinism: Retrospective study with genotype correlations

Pediatric and Developmental Pathology

Volumn 6, Issue 4, 2003, Pages 322-333

  Suchi, Mariko ^a   MacMullen, Courtney ^a   Thornton, Paul S ^a   Ganguly, Arupa ^a   Stanley, Charles A ^a   Ruchelli, Eduardo D ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Adenomatosis; Hyperinsulinism; Nesidioblastosis; Pancreas; Potassium channel; Sulphonylurea receptor

Indexed keywords

ADENOSINE TRIPHOSPHATE; GENOMIC DNA; INWARDLY RECTIFYING POTASSIUM CHANNEL; POTASSIUM CHANNEL; SULFONYLUREA RECEPTOR;

ABCC8 GENE; ARTICLE; CLINICAL ARTICLE; CORRELATION ANALYSIS; EXON; FEMALE; GENE; GENE MUTATION; GENETIC DISORDER; GENOTYPE; GLUCOSE BLOOD LEVEL; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERINSULINISM; INFANT; KCNJ11 GENE; MALE; NEWBORN; PANCREAS RESECTION; PRIORITY JOURNAL; RETROSPECTIVE STUDY;

ATP-BINDING CASSETTE TRANSPORTERS; BLOOD GLUCOSE; CASE-CONTROL STUDIES; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; HYPERINSULINISM; INFANT; INFANT, NEWBORN; MUTATION; PANCREAS; POINT MUTATION; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG; RETROSPECTIVE STUDIES;

EID: 0141650394     PISSN: 10935266     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10024-002-0026-9     Document Type: Article

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