Hyperinsulinemic hypoglycemia syndrome associated with mutations in the human insulin receptor gene: Report of two cases-Reference-Cited by-同舟云学术

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Hyperinsulinemic hypoglycemia syndrome associated with mutations in the human insulin receptor gene: Report of two cases

Published:2015 Issue:4 Volume:62 Page:353-362
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Kuroda Yohei¹,Iwahashi Hiromi²¹,Mineo Ikuo³,Fukui Kenji¹,Fukuhara Atsunori¹,Iwamoto Ryuya¹,Imagawa Akihisa¹,Shimomura Iichiro¹

Affiliation:

1. Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan

2. Department of Diabetes Care Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan

3. Diabetes Center, Toyonaka Municipal Hospital, Toyonaka, Osaka, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference27 articles.

1. 1. Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, et al. (1995) Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 268:426-429.

2. 2. Thomas P, Ye Y, Lightner E (1996) Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet 5:1809-1812.

3. 3. Kapoor RR, James C, Hussain K (2009) Advances in the diagnosis and management of hyperinsulinemic hypoglycemia. Nat Clin Pract Endocrinol Metab 5:101-112.

4. 4. Placzkowski KA, Vella A, Thompson GB, Grant CS, Reading CC, et al. (2009) Secular trends in the presentation and management of functioning insulinoma at the Mayo Clinic, 1987-2007. J Clin Endocrinol Metab 94:1069-1073.

5. 5. Hirata Y, Uchigata Y (1994) Insulin autoimmune syndrome in Japan. Diabetes Res Clin Pract Suppl:S153-157.

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