1-6 of 6
Jean-Jacques Robert
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

ZnT8 Is a Major CD8+ T Cell–Recognized Autoantigen in Pediatric Type 1 Diabetes

Émmanuelle Énée, Roland Kratzer, Jean-Baptiste Arnoux, Emilie Barilleau, Yamina Hamel, Christophe Marchi, Jacques Beltrand, Bénédicte Michaud, Lucienne Chatenoud, Jean-Jacques Robert, Peter van Endert
Journal: Diabetes
Diabetes 2012;61(7):1779–1784
https://doi.org/10.2337/db12-0071
Published: 15 June 2012
View article titled, ZnT8 Is a Major CD8<sup>+</sup> T Cell–Recognized Autoantigen in Pediatric Type 1 Diabetes
Open the PDF for ZnT8 Is a Major CD8<sup>+</sup> T Cell–Recognized Autoantigen in Pediatric Type 1 Diabetes in another window
Includes: Supplementary data
Journal Articles

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

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: <subtitle>Clinical, Genetic, and Functional Study of <em>EIF2AK3</em> Mutations and Suggestion of Genetic Heterogeneity</subtitle>
Open the PDF for Wolcott-Rallison Syndrome: <subtitle>Clinical, Genetic, and Functional Study of <em>EIF2AK3</em> Mutations and Suggestion of Genetic Heterogeneity</subtitle> in another window
Journal Articles

Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies

Jocelyne Magré, Marc Delépine, Lionel Van Maldergem, Jean-Jacques Robert, J. Antonie Maassen, Muriel Meier, Vanessa R. Panz, Chong Ae Kim, Nadia Tubiana-Rufi, Paul Czernichow, Eva Seemanova, Charles R. Buchanan, Didier Lacombe, Corinne Vigouroux, Olivier Lascols, C. Ronald Kahn, Jacqueline Capeau, Mark Lathrop
Journal: Diabetes
Diabetes 2003;52(6):1573–1578
https://doi.org/10.2337/diabetes.52.6.1573
Published: 01 June 2003
View article titled, Prevalence of Mutations in <em>AGPAT2</em> Among Human Lipodystrophies
Open the PDF for Prevalence of Mutations in <em>AGPAT2</em> Among Human Lipodystrophies in another window
Journal Articles

Clinical Phenotypes, Insulin Secretion, and Insulin Sensitivity in Kindreds With Maternally Inherited Diabetes and Deafness Due to Mitochondrial tRNALeu(UUR) Gene Mutation

Gilberto Velho, Maria M Byrne, Karine Clément, Jeppe Sturis, Maria E. Pueyo, Helène Blanché, Nathalie Vionnet, Jean Fiet, Philippe Passa, Jean-Jacques Robert, Kenneth S Polonsky, Philippe Froguel
Journal: Diabetes
Diabetes 1996;45(4):478–487
https://doi.org/10.2337/diab.45.4.478
Published: 01 April 1996
View article titled, Clinical Phenotypes, Insulin Secretion, and Insulin Sensitivity in Kindreds With Maternally Inherited Diabetes and Deafness Due to Mitochondrial tRNA<sup>Leu(UUR)</sup> Gene Mutation
Open the PDF for Clinical Phenotypes, Insulin Secretion, and Insulin Sensitivity in Kindreds With Maternally Inherited Diabetes and Deafness Due to Mitochondrial tRNA<sup>Leu(UUR)</sup> Gene Mutation in another window
Journal Articles

Six Mutations in the Glucokinase Gene Identified in MODY by Using a Nonradioactive Sensitive Screening Technique

Jörg Hager, Hélène Blanché, Fang Sun, Nathalie Vionnet Martine Vaxillaire, Wolfgang Poller, Daniel Cohen, Paul Czernichow, Gilberto Velho, Jean-Jacques Robert, Nadine Cohen, Philippe Froguel
Journal: Diabetes
Diabetes 1994;43(5):730–733
https://doi.org/10.2337/diab.43.5.730
Published: 01 May 1994
View article titled, Six Mutations in the Glucokinase Gene Identified in MODY by Using a Nonradioactive Sensitive Screening Technique
Open the PDF for Six Mutations in the Glucokinase Gene Identified in MODY by Using a Nonradioactive Sensitive Screening Technique in another window
Journal Articles

Whole Body De Novo Amino Acid Synthesis in Type I (Insulin-dependent) Diabetes Studied With Stable Isotope-labeled Leucine, Alanine, and Glycine

Jean Jacques Robert, Bernard Beaufrere, Joseph Koziet, Jehan Francois Desjeux, Dennis M Bier, Vernon R Young, Henri Lestradet
Journal: Diabetes
Diabetes 1985;34(1):67–73
https://doi.org/10.2337/diab.34.1.67
Published: 01 January 1985
View article titled, Whole Body De Novo Amino Acid Synthesis in Type I (Insulin-dependent) Diabetes Studied With Stable Isotope-labeled Leucine, Alanine, and Glycine
Open the PDF for Whole Body De Novo Amino Acid Synthesis in Type I (Insulin-dependent) Diabetes Studied With Stable Isotope-labeled Leucine, Alanine, and Glycine in another window