Successful maintenance on sulphonylurea therapy and low diabetes complication rates in a HNF1A-MODY cohort-Reference-Cited by-同舟云学术

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Successful maintenance on sulphonylurea therapy and low diabetes complication rates in a HNF1A-MODY cohort

Published:2015-11-17 Issue:7 Volume:33 Page:976-984
ISSN:0742-3071
Container-title:Diabetic Medicine
language:en
Short-container-title:Diabet. Med.

Author:

Bacon S.¹,Kyithar M. P.¹,Rizvi S. R.¹,Donnelly E.¹,McCarthy A.¹,Burke M.¹,Colclough K.²,Ellard S.²³,Byrne M. M.¹

Affiliation:

1. Department of Diabetes & Endocrinology; Mater Misericordiae University Hospital; Dublin Ireland

2. Department of Molecular Genetics; Royal Devon & Exeter NHS Foundation Trust; Exeter UK

3. Institute of Biomedical and Clinical Science; University of Exeter Medical School; Exeter UK

Funder

Health Research Board

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/dme.12992/fullpdf

Reference27 articles.

1. Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes;Murphy;Nat Clin Pract Endocrinol Metab,2008

2. Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K;Frayling;Diabetes,1997

3. High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes;Lehto;Diabetologia,1999

4. Early-onset Type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor 1alpha and glucokinase;Gragnoli;Diabetologia,2001

5. Identification of HNF1A-MODY and HNF4A-MODY in Irish families: phenotypic characteristics and therapeutic implications;Kyithar;Diabetes Metab,2011

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