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Cécile Saint-Martin
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Journal Articles

Long-term Metabolic and Socioeducational Outcomes of Transient Neonatal Diabetes: A Longitudinal and Cross-sectional Study

Fleur Le Bourgeois, Jacques Beltrand, Baz Baz, Jean-Baptiste Julla, Jean-Pierre Riveline, Albane Simon, Isabelle Flechtner, Malek Ait Djoudi, Anne-Laure Fauret-Amsellem, Yoann Vial, Raphael Scharfmann, Julie Sommet, Philippe Boudou, Hélène Cavé, Michel Polak, Jean-François Gautier, Kanetee Busiah, TNDM Long-Term Follow-Up Study Group, Sawsan Abu-Amara Olivieri, Nadège Bachere, Christine Bellanne-Chantelot, Anne-Marie Bertrand, Olivier Bourron, Fabienne De Boisvilliers, Bernard Deumier, Pierre Gourdy, Agnès Hartemann, Stephanie Jellimann, Claire Le Tallec, Amélie Martin-Dessilla, Anne Paoli, Mireille Perrin, Jean Ribstein, Cécile Saint-Martin, Charles Thivolet, Bernard Vialettes, Hubert Ythier
Journal: Diabetes Care
Diabetes Care 2020;43(6):1191–1199
https://doi.org/10.2337/dc19-0324
Published: 09 April 2020
View article titled, Long-term Metabolic and Socioeducational Outcomes of Transient Neonatal Diabetes: A Longitudinal and Cross-sectional Study
Open the PDF for Long-term Metabolic and Socioeducational Outcomes of Transient Neonatal Diabetes: A Longitudinal and Cross-sectional Study in another window
Includes: Supplementary data
Journal Articles

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

Danièle Dubois-Laforgue, Erika Cornu, Cécile Saint-Martin, Joël Coste, Christine Bellanné-Chantelot, José Timsit
Journal: Diabetes Care
Diabetes Care 2018;41(1):e8–e9
https://doi.org/10.2337/dci17-0048
Published: 11 December 2017
View article titled, 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 (<em>HNF1B</em>) Molecular Defects. Diabetes Care 2017;40:1436–1443
Open the PDF for 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 (<em>HNF1B</em>) Molecular Defects. Diabetes Care 2017;40:1436–1443 in another window
Journal Articles

Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B (HNF1B) Molecular Defects

Danièle Dubois-Laforgue, Erika Cornu, Cécile Saint-Martin, Joël Coste, Christine Bellanné-Chantelot, José Timsit, for the Monogenic Diabetes Study Group of the Société Francophone du Diabète
Journal: Diabetes Care
Diabetes Care 2017;40(11):1436–1443
https://doi.org/10.2337/dc16-2462
Published: 18 April 2017
View article titled, Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B (<em>HNF1B</em>) Molecular Defects
Open the PDF for Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B (<em>HNF1B</em>) Molecular Defects in another window
Includes: Supplementary data
Journal Articles

Incretin Effect of Glucagon-Like Peptide 1 Receptor Agonist Is Preserved in Presence of ABCC8/SUR1 Mutation in β -Cell

Olivier Bourron, MD, PHD, Fatma Chebbi, MD, Marine Halbron, MD, Cécile Saint-Martin, MD, Christine Bellanné-Chantelot, MD, PHD, Ahmed Abed, MD, Beny Charbit, MD, PHD, Christophe Magnan, MD, PHD, J.M. Lacorte, MD, PHD, Agnès Hartemann, MD, PHD
Journal: Diabetes Care
Diabetes Care 2012;35(11):e76
https://doi.org/10.2337/dc12-0535
Published: 13 October 2012
View article titled, Incretin Effect of Glucagon-Like Peptide 1 Receptor Agonist Is Preserved in Presence of ABCC8/SUR1 Mutation in β -Cell
Open the PDF for Incretin Effect of Glucagon-Like Peptide 1 Receptor Agonist Is Preserved in Presence of ABCC8/SUR1 Mutation in β -Cell in another window