메뉴 건너뛰기




Volumn 7, Issue 1, 2002, Pages 95-100

Persistent hyperinsulinaemic hypoglycaemia

Author keywords

Diazoxide; Diffuse CI; Focal CI; Glucagon; GLUD1 gene; Hyperammonaemia; Hyperinsulinism; KIR6.2 gene; PHHI; Somatostatine; SUR1 gene

Indexed keywords

ARTICLE; BRAIN INJURY; DIAGNOSTIC TEST; ENZYME ACTIVITY; FEMALE; GLUCOSE BLOOD LEVEL; HISTOPATHOLOGY; HUMAN; HYPERINSULINEMIA; HYPOGLYCEMIA; INBORN ERROR OF METABOLISM; INFANT; INSULIN RELEASE; MACROSOMIA; MAJOR CLINICAL STUDY; MALE; NEWBORN; NEWBORN PERIOD; NEWBORN SCREENING; PANCREAS RESECTION; PROGNOSIS;

EID: 0036306878     PISSN: 10842756     EISSN: None     Source Type: Journal    
DOI: 10.1053/siny.2001.0090     Document Type: Article
Times cited : (26)

References (34)
  • 10
  • 13
    • 0030880778 scopus 로고    scopus 로고
    • Somatic deletion of the imprinted 11p15 region in sporadic persistent hyper-insulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy
    • (1997) J Clin Invest , vol.100 , pp. 802-807
    • De Lonlay, P.1    Fournet, J.C.2    Rahier, J.3
  • 14
    • 0032190017 scopus 로고    scopus 로고
    • Maternal allele loss with somatic reduction to homozygosity of the paternally-inherited mutation of the SUR1 gene leads to congenital hyperinsulinism in focal islet cell adenomatous hyperplasia of the pancreas
    • (1998) J Clin Invest , vol.102 , pp. 1286-1291
    • Verkarre, V.1    Fournet, J.C.2    De Lonlay, P.3
  • 17
    • 0021320297 scopus 로고
    • The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: Deficiency of pancreatic D cells or hyperactivity of B cells?
    • (1984) Diabetologia , vol.26 , pp. 282-289
    • Rahier, J.1    Fält, K.2    Müntefering, H.3
  • 19
    • 0029098644 scopus 로고
    • Hyperinsulinism in children: Diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases
    • (1995) Pediatr Radiol , vol.25 , pp. 512-516
    • Dubois, J.1    Brunelle, F.2    Touati, G.3
  • 23
    • 0034970925 scopus 로고    scopus 로고
    • Molecular study of 31 focal forms of persistent hyperinsulinemic hypoglycemia of infancy (CI): Association of a reduction to homozygosity of a SUR1/KIR6.2 mutation and unbalanced expression of 11p15 imprinted genes
    • (2001) Am J Pathol , vol.158 , pp. 2177-2184
    • Fournet, J.C.1    Mayaud, C.2    De Lonlay, P.3
  • 26
    • 0029836983 scopus 로고    scopus 로고
    • Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
    • (1996) Hum Molec Genet , vol.5 , pp. 1813-1822
    • Thomas, P.1    Ye, Y.2    Lightner, E.3
  • 30
    • 0023828816 scopus 로고
    • Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
    • (1988) Nature , vol.332 , pp. 85-87
    • Larsson, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.