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Marc Nicolino
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Meeting Abstracts

314-OR: Improved Outcomes across Baseline Time-in-Range Levels with the Omnipod 5 AID System Compared with Multiple Daily Injections (MDI) in Type 1 Diabetes (T1D)—Analysis of the RADIANT Study

Free
EMMA G. WILMOT, JACQUES BELTRAND, BRUNO GUERCI, AURÉLIE BEROT, HÉLÈNE HANAIRE, ELISE BISMUTH, PIETER GILLARD, MARIE-BÉATRICE SAADE, MICHAEL JOUBERT, RANDA SALET, PRATIK CHOUDHARY, RACHEL REYNAUD, LALANTHA LEELARATHNA, EMELINE RENARD, SANDRINE LABLANCHE, CECILE GOUILLARD DARNAUD, SZE M. NG, PHILIPPE A. LYSY, NIKOLAOS DASKAS, KEVIN PERGE, THOMAS S. CRABTREE, TRANG T. LY, MARC NICOLINO, RADIANT STUDY GROUP
Journal: Diabetes
Diabetes 2025;74(Supplement_1):314-OR
https://doi.org/10.2337/db25-314-OR
Published: 20 June 2025
View article titled, 314-OR: Improved Outcomes across Baseline Time-in-Range Levels with the Omnipod 5 AID System Compared with Multiple Daily Injections (MDI) in Type 1 Diabetes (T1D)—Analysis of the RADIANT Study
Journal Articles

dUTPase (DUT) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure

Free
Reinaldo Sousa Dos Santos, Mathilde Daures, Anne Philippi, Sophie Romero, Lorella Marselli, Piero Marchetti, Valérie Senée, Delphine Bacq, Céline Besse, Baz Baz, Laura Marroquí, Sarah Ivanoff, Julien Masliah-Planchon, Marc Nicolino, Jean Soulier, Gérard Socié, Decio L. Eizirik, Jean-François Gautier, Cécile Julier
Journal: Diabetes
Diabetes 2017;66(4):1086–1096
https://doi.org/10.2337/db16-0839
Published: 10 January 2017
View article titled, dUTPase (DUT) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure
Open the PDF for dUTPase (DUT) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure in another window
Includes: Supplementary data
Journal Articles

A Missense Mutation in PPP1R15B Causes a Syndrome Including Diabetes, Short Stature, and Microcephaly

Free
Baroj Abdulkarim, Marc Nicolino, Mariana Igoillo-Esteve, Mathilde Daures, Sophie Romero, Anne Philippi, Valérie Senée, Miguel Lopes, Daniel A. Cunha, Heather P. Harding, Céline Derbois, Nathalie Bendelac, Andrew T. Hattersley, Décio L. Eizirik, David Ron, Miriam Cnop, Cécile Julier
Journal: Diabetes
Diabetes 2015;64(11):3951–3962
https://doi.org/10.2337/db15-0477
Published: 09 July 2015
View article titled, A Missense Mutation in PPP1R15B Causes a Syndrome Including Diabetes, Short Stature, and Microcephaly
Open the PDF for A Missense Mutation in PPP1R15B Causes a Syndrome Including Diabetes, Short Stature, and Microcephaly in another window
Includes: Supplementary data
Journal Articles

A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency

Open Access
Marc Nicolino, Kathryn C. Claiborn, Valérie Senée, Anne Boland, Doris A. Stoffers, Cécile Julier
Journal: Diabetes
Diabetes 2010;59(3):733–740
https://doi.org/10.2337/db09-1284
Published: 15 December 2009
View article titled, A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency
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Includes: Supplementary data
Journal Articles

Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (TCF2) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5

Free
Christine Bellanné-Chantelot, Séverine Clauin, Dominique Chauveau, Philippe Collin, Michèle Daumont, Claire Douillard, Danièle Dubois-Laforgue, Laurent Dusselier, Jean-François Gautier, Michel Jadoul, Marie Laloi-Michelin, Laetitia Jacquesson, Etienne Larger, Jacques Louis, Marc Nicolino, Jean-François Subra, Jean-Marie Wilhem, Jacques Young, Gilberto Velho, José Timsit
Journal: Diabetes
Diabetes 2005;54(11):3126–3132
https://doi.org/10.2337/diabetes.54.11.3126
Published: 01 November 2005
View article titled, Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (TCF2) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5
Open the PDF for Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (TCF2) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5 in another window
Includes: Supplementary data
Journal Articles

Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity

Free
Valérie Senée, Krishna M. Vattem, Marc Delépine, Lynn A. Rainbow, Céline Haton, Annick Lecoq, Nick J. Shaw, Jean-Jacques Robert, Raoul Rooman, Catherine Diatloff-Zito, Jacques L. Michaud, Bassan Bin-Abbas, Doris Taha, Bernard Zabel, Piergiorgio Franceschini, A. Kemal Topaloglu, G. Mark Lathrop, Timothy G. Barrett, Marc Nicolino, Ronald C. Wek, Cécile Julier
Journal: Diabetes
Diabetes 2004;53(7):1876–1883
https://doi.org/10.2337/diabetes.53.7.1876
Published: 01 July 2004
View article titled, Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity
Open the PDF for Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity in another window