A case of familial nesidioblastosis: prenatal diagnosis of foetal hyperinsulinism
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1992.tb12121.x/fullpdf
Reference15 articles.
1. Serum glutathione S-transferase in experimentl liver damage in rats
2. The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: deficiency of pancreatic D cells or hyperactivity of B cells?
3. Idiopathic hypoglycaemia in sibs with morphological evidence of nesidioblastosis of the pancreas.
4. Familial nesidioblastosis: Severe neonatal hypoglycemia in two families
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1. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
2. Early brain atrophy in persistent hyperinsulinemic hypoglycemia of infancy;The Journal of Pediatrics;2002-11
3. Antepartum Findings and Obstetric Aspects in Pregnancies Followed by Neonatal Persistent Hyperinsulinemic Hypoglycemia;American Journal of Perinatology;2002
4. Ten years' experience of persistent hyperinsulinaemic hypoglycaemia of infancy;Journal of Paediatrics and Child Health;2001-10-14
5. Macrosomia: A Genetic Perspective;Clinical Obstetrics and Gynecology;2000-06
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