Nesidioblastosis: evidence for autosomal recessive inheritance.

Author:

Woolf D A,Leonard J V,Trembath R C,Pembrey M E,Grant D B

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference4 articles.

1. Autosomal recessive phenotypes. Mendelian inheritance in man;Mckusick, V.A.

2. Idiopathic hypoglycaemia in sibs with morphological evidence of nesidioblastosis of the pancreas;Woo, D.; Scopes, J.W.; Polak, J.M.;Arch Dis Child,1976

3. The pancreatic islet of infants with severe hypoglycaemia;Misugi, K.; Misugi, N.; Sotos, J.; Smith, B.;Archives of Pathology,1970

4. Familial hyperinsulinism with nesidioblastosis of the pancreas: further evidence for autosomal recessive inheritance;Moreno, L.A.; Turck, D.; Gottrand, F.; Fabre, M.; ManouvrierHanu, S.; Farriaux, J.P.;Am J Med Genet,1989

Cited by 36 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

2. Clinical and genetic heterogeneity in congenital hyperinsulinism;European Journal of Pediatrics;2001-11-07

3. Nesidioblastosis and Persistent Hyperinsulinemic Hypoglycemia: Are They Related?;Pathology Case Reviews;2001-05

4. The KATP Channel and the Sulfonylurea Receptor;Molecular Basis of Pancreas Development and Function;2001

5. Hyperinsulinism of the newborn;Seminars in Perinatology;2000-04

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