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Year | Number of Results |
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MODY associated with two novel hepatocyte nuclear factor-1alpha loss-of-function mutations (P112L and Q466X).
Biochem Biophys Res Commun. 2000 Dec 29;279(3):792-8. doi: 10.1006/bbrc.2000.4024.
Biochem Biophys Res Commun. 2000.
PMID: 11162430
Persistently autoantibody negative (PAN) type 1 diabetes mellitus in children.
Hameed S, Ellard S, Woodhead HJ, Neville KA, Walker JL, Craig ME, Armstrong T, Yu L, Eisenbarth GS, Hattersley AT, Verge CF.
Hameed S, et al.
Pediatr Diabetes. 2011 May;12(3 Pt 1):142-9. doi: 10.1111/j.1399-5448.2010.00681.x. Epub 2010 Sep 6.
Pediatr Diabetes. 2011.
PMID: 21518407
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Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population.
Najmi LA, Aukrust I, Flannick J, Molnes J, Burtt N, Molven A, Groop L, Altshuler D, Johansson S, Bjørkhaug L, Njølstad PR.
Najmi LA, et al.
Diabetes. 2017 Feb;66(2):335-346. doi: 10.2337/db16-0460. Epub 2016 Nov 29.
Diabetes. 2017.
PMID: 27899486
Free PMC article.
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Clinical and genetic characterization and long-term evaluation of individuals with maturity-onset diabetes of the young (MODY): The journey towards appropriate treatment.
Campos Franco P, Santos de Santana L, Dantas Costa-Riquetto A, Santomauro Junior AC, Jorge AAL, Gurgel Teles M.
Campos Franco P, et al.
Diabetes Res Clin Pract. 2022 May;187:109875. doi: 10.1016/j.diabres.2022.109875. Epub 2022 Apr 25.
Diabetes Res Clin Pract. 2022.
PMID: 35472491
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