Treatment with long-acting lanreotide autogel in early infancy in patients with severe neonatal hyperinsulinism-Reference-Cited by-同舟云学术

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Treatment with long-acting lanreotide autogel in early infancy in patients with severe neonatal hyperinsulinism

Published:2017-06-02 Issue:1 Volume:12 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Corda Heike,Kummer Sebastian,Welters Alena,Teig Norbert,Klee Dirk,Mayatepek Ertan,Meissner Thomas

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-017-0653-x.pdf

Reference37 articles.

1. James C, Kapoor RR, Ismail D, Hussain K. The genetic basis of congenital hyperinsulinism. J Med Genet. 2009;46:289–99.

2. Arya VB, Mohammed Z, Blankenstein O, de Lonlay P, Hussain K. Hyperinsulinaemic hypoclycemia. Horm Metab Res. 2014;46:157–70.

3. Hussain K. Diagnosis and management of hyperinsulinaemic hypoglycaemia of infancy. Horm Res. 2008;69:2–13.

4. Romanelli V, et al. CDKN1C (p57Kip2) Analysis in Beckwith-Wiedemann Syndrome (BWS) patients: genotype-phenotype correlations, novel mutations, and polymorphisms. Am J Med Genet Part A. 2010;152A:1390–97.

5. Arnoux J-B, Verkarre V, Rossignol S, Aigrain Y, de Lonlay P. Molecular mechanisms and clinical pathophysiologies of focal ATP-sensitive potassium channel hyperinsulinism and Beckwith-Wiedemann Syndrome. Hyperinsulinemic Hypoglycemia Disordes. Front Diabtetes Karger. 2012;21:43–56.

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