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Clinical characteristics and diagnostic criteria of maturity-onset diabetes of the young (MODY) due to molecular anomalies of the HNF1A gene.
Bellanné-Chantelot C, Lévy DJ, Carette C, Saint-Martin C, Riveline JP, Larger E, Valéro R, Gautier JF, Reznik Y, Sola A, Hartemann A, Laboureau-Soares S, Laloi-Michelin M, Lecomte P, Chaillous L, Dubois-Laforgue D, Timsit J; French Monogenic Diabetes Study Group. Bellanné-Chantelot C, et al. J Clin Endocrinol Metab. 2011 Aug;96(8):E1346-51. doi: 10.1210/jc.2011-0268. Epub 2011 Jun 15. J Clin Endocrinol Metab. 2011. PMID: 21677039 Free article.
Clinical utility gene card for: Maturity-onset diabetes of the young.
Colclough K, Saint-Martin C, Timsit J, Ellard S, Bellanné-Chantelot C. Colclough K, et al. Eur J Hum Genet. 2014 Sep;22(9). doi: 10.1038/ejhg.2014.14. Epub 2014 Feb 12. Eur J Hum Genet. 2014. PMID: 24518839 Free PMC article. No abstract available.
Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B (HNF1B) Molecular Defects.
Dubois-Laforgue D, Cornu E, Saint-Martin C, Coste J, Bellanné-Chantelot C, Timsit J; Monogenic Diabetes Study Group of the Société Francophone du Diabète. Dubois-Laforgue D, et al. Diabetes Care. 2017 Nov;40(11):1436-1443. doi: 10.2337/dc16-2462. Epub 2017 Apr 18. Diabetes Care. 2017. PMID: 28420700
High-sensitivity C-reactive protein does not improve the differential diagnosis of HNF1A-MODY and familial young-onset type 2 diabetes: A grey zone analysis.
Bellanné-Chantelot C, Coste J, Ciangura C, Fonfrède M, Saint-Martin C, Bouché C, Sonnet E, Valéro R, Lévy DJ, Dubois-Laforgue D, Timsit J; Monogenic Diabetes Study Group of the Société Francophone du Diabète (SFD). Bellanné-Chantelot C, et al. Diabetes Metab. 2016 Feb;42(1):33-7. doi: 10.1016/j.diabet.2015.02.001. Epub 2015 Mar 6. Diabetes Metab. 2016. PMID: 25753245
Response to Comment on Dubois-Laforgue et al. Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B (HNF1B) Molecular Defects. Diabetes Care 2017;40:1436-1443.
Dubois-Laforgue D, Cornu E, Saint-Martin C, Coste J, Bellanné-Chantelot C, Timsit J. Dubois-Laforgue D, et al. Diabetes Care. 2018 Jan;41(1):e8-e9. doi: 10.2337/dci17-0048. Diabetes Care. 2018. PMID: 29263198 No abstract available.
Next-generation sequencing identifies monogenic diabetes in 16% of patients with late adolescence/adult-onset diabetes selected on a clinical basis: a cross-sectional analysis.
Donath X, Saint-Martin C, Dubois-Laforgue D, Rajasingham R, Mifsud F, Ciangura C, Timsit J, Bellanné-Chantelot C; Monogenic Diabetes Study Group of the Société Francophone du Diabète. Donath X, et al. BMC Med. 2019 Jul 11;17(1):132. doi: 10.1186/s12916-019-1363-0. BMC Med. 2019. PMID: 31291970 Free PMC article.
209 results