نتائج البحث - Jean‐Jacques Robert

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  1. 1
    Long-Term Follow-Up of Oral Glucose Tolerance Test–Derived Glucose Tolerance and Insulin Secretion and Insulin Sensitivity Indexes in Subjects With Glucokinase Mutations (MODY2)

    Long-Term Follow-Up of Oral Glucose Tolerance Test–Derived Glucose Tolerance and Insulin Secretion and Insulin Sensitivity Indexes in Subjects With Glucokinase Mutations (MODY2) حسب Delphine Martin, Christine Bellanné‐Chantelot, Inge Deschamps, Philippe Froguel, Jean‐Jacques Robert, Gilberto Velho

    منشور في 2008
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    Artigo
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  2. 2
    Recommendations for age-appropriate education of children and adolescents with diabetes and their parents in the European Union

    Recommendations for age-appropriate education of children and adolescents with diabetes and their parents in the European Union حسب Delphine Martin, Karin Lange, Alexandra Sima, Dagmar Kownatka, Søren Skovlund, Thomas Danne, Jean‐Jacques Robert

    منشور في 2012
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    Artigo
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  3. 3
    Intrastriatal injection of an adenoviral vector expressing glial-cell-line-derived neurotrophic factor prevents dopaminergic neuron degeneration and behavioral impairment in a rat model of Parkinson disease

    Intrastriatal injection of an adenoviral vector expressing glial-cell-line-derived neurotrophic factor prevents dopaminergic neuron degeneration and behavioral impairment in a rat... حسب Alicia Bilang‐Bleuel, Frédéric Revah, Phillippe Colin, Isabelle Locquet, Jean‐Jacques Robert, Jacques Mallet, Philippe Horellou

    منشور في 1997
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    Artigo
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  4. 4
    Adipose Tissue IL-6 Content Correlates with Resistance to Insulin Activation of Glucose Uptake both in Vivo and in Vitro

    Adipose Tissue IL-6 Content Correlates with Resistance to Insulin Activation of Glucose Uptake both in Vivo and in Vitro حسب Jean‐Philippe Bastard, Mustapha Maachi, Jeanne Tran Van Nhieu, Claude Jardel, Éric Bruckert, André Grimaldi, Jean‐Jacques Robert, Jacqueline Capeau, Bernard Hainque

    منشور في 2002
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    Artigo
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  5. 5
    KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features

    KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features حسب Anna L. Gloyn, C. Diatloff‐Zito, Emma L. Edghill, Christine Bellanné‐Chantelot, Sylvie Nivot, R. Coutant, Sian Ellard, Andrew T. Hattersley, Jean Jacques Robert

    منشور في 2006
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    Artigo
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  6. 6
    ZnT8 Is a Major CD8+ T Cell–Recognized Autoantigen in Pediatric Type 1 Diabetes

    ZnT8 Is a Major CD8+ T Cell–Recognized Autoantigen in Pediatric Type 1 Diabetes حسب Emmanuelle Énée, Roland Kratzer, Jean‐Baptiste Arnoux, Émilie Barilleau, Yamina Hamel, Christophe Marchi, Jacques Beltrand, Bénédicte Michaud, Lucienne Chatenoud, Jean‐Jacques Robert, Peter Van Endert

    منشور في 2012
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  7. 7
    Glucose Metabolism in 105 Children and Adolescents After Pancreatectomy for Congenital Hyperinsulinism

    Glucose Metabolism in 105 Children and Adolescents After Pancreatectomy for Congenital Hyperinsulinism حسب Jacques Beltrand, Marylène Caquard, Jean‐Baptiste Arnoux, Kathleen Laborde, Gilberto Velho, Virginie Verkarre, Jacques Rahier, Françis Brunelle, Claire Nihoul‐Feketé, Jean‐Marie Saudubray, Jean‐Jacques Robert, Pascale de Lonlay

    منشور في 2011
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    Artigo
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  8. 8
    GAD65 Antigen Therapy in Recently Diagnosed Type 1 Diabetes Mellitus

    GAD65 Antigen Therapy in Recently Diagnosed Type 1 Diabetes Mellitus حسب Johnny Ludvigsson, David Krisky, Rosaura Casas, Tadej Battelino, Luís Castaño, James Greening, Olga Kordonouri, Timo Otonkoski, Paolo Pozzilli, Jean‐Jacques Robert, Henk J. Veeze, Jerry P. Palmer, Diamyd Medical

    منشور في 2012
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  9. 9
    Congenital hyperinsulinism: current trends in diagnosis and therapy

    Congenital hyperinsulinism: current trends in diagnosis and therapy حسب Jean-Baptiste Arnoux, Virginie Verkarre, Cécile Saint‐Martin, Françoise Montravers, Anaïs Brassier, Vassili Valayannopoulos, Françis Brunelle, Jean-Christophe Fournet, Jean-Jacques Robert, Y. Aigrain, Christine Bellanné‐Chantelot, Pascale de Lonlay

    منشور في 2011
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    Revisão
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  10. 10
    Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism

    Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism حسب Jean‐Christophe Fournet, Christine Mayaud, Pascale de Lonlay, M S Gross-Morand, Virginie Verkarre, Mireille Castanet, Martine Devillers, Jacques Rahier, Françis Brunelle, Jean‐Jacques Robert, Claire Nihoul‐Feketé, Jean‐Marie Saudubray, Claudine Junien

    منشور في 2001
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    Artigo
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  11. 11
    Clinical Features of 52 Neonates with Hyperinsulinism

    Clinical Features of 52 Neonates with Hyperinsulinism حسب Pascale de Lonlay-Debeney, F Poggi-Travert, Jean‐Christophe Fournet, Christine Sempoux, Carlo Dionisi‐Vici, Françis Brunelle, Guy Touati, Jacques Rahier, Claudine Junien, Claire Nihoul‐Feketé, Jean‐Jacques Robert, Jean‐Marie Saudubray

    منشور في 1999
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    Artigo
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  12. 12
    Serum leptin level is a regulator of bone mass

    Serum leptin level is a regulator of bone mass حسب Florent Elefteriou, S. Takeda, Ken Ebihara, Jocelyne Magré, N. Patano, Chong Ae Kim, Yoshihiro Ogawa, X. Liu, Stephanie M. Ware, William J. Craigen, Jean‐Jacques Robert, Charles Vinson, Kazuwa Nakao, Jacqueline Capeau, Gérard Karsenty

    منشور في 2004
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    Artigo
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  13. 13
    Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy.

    Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pan... حسب Pascale de Lonlay, Jean Fournet, Jacques Rahier, M S Gross-Morand, F Poggi-Travert, V. Foussier, Jean‐Paul Bonnefont, M.C. Brusset, Françis Brunelle, Jean Jacques Robert, Claire Nihoul‐Feketé, Jean‐Marie Saudubray, Claudine Junien

    منشور في 1997
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    Artigo
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  14. 14
    Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families

    Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families حسب Gilberto Velho, Hélène Blanché, Martine Vaxillaire, Christine Bellanné‐Chantelot, Victor Cavalcanti Pardini, José Timsit, P Passa, I Deschamps, Jean‐Jacques Robert, Irene T. Weber, Diane Marotta, S.J. Pilkis, Gregory M. Lipkind, Graeme I. Bell, Philippe Froguel

    منشور في 1997
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    Artigo
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  15. 15
    Congenital Hyperinsulinism: Pancreatic [<sup>18</sup>F]Fluoro-<scp>l</scp>-Dihydroxyphenylalanine (DOPA) Positron Emission Tomography and Immunohistochemistry Study of DOPA Decarboxylase and Insulin Secretion

    Congenital Hyperinsulinism: Pancreatic [<sup>18</sup>F]Fluoro-<scp>l</scp>-Dihydroxyphenylalanine (DOPA) Positron Emission Tomography and Immunohistochemistry Study of DOPA Decarbo... حسب Pascale de Lonlay, Aurore Simon-Carré, Maria-João Ribeiro, Nathalie Boddaert, Irina Giurgea, Kathleen Laborde, Christine Bellanné‐Chantelot, Virginie Verkarre, Michel Polak, Jacques Rahier, André Syrota, David Seidenwurm, Claire Nihoul‐Feketé, Jean‐Jacques Robert, Françis Brunelle, Francis Jaubert

    منشور في 2006
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    Artigo
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  16. 16
    Prevalence of Mutations in <i>AGPAT2</i> Among Human Lipodystrophies

    Prevalence of Mutations in <i>AGPAT2</i> Among Human Lipodystrophies حسب Jocelyne Magré, Marc Délepine, Lionel Van Maldergem, Jean‐Jacques Robert, J. Antonie Maassen, Muriel Meier, Vanessa R. Panz, Chong Ae Kim, Nadia Tubiana‐Rufi, Paul Czernichow, E Seemanová, Charles Buchanan, Didier Lacombe, Corinne Vigouroux, Olivier Lascols, C. Ronald Kahn, Jacqueline Capeau, Mark Lathrop

    منشور في 2003
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  17. 17
    Switching from Insulin to Oral Sulfonylureas in Patients with Diabetes Due to Kir6.2 Mutations

    Switching from Insulin to Oral Sulfonylureas in Patients with Diabetes Due to Kir6.2 Mutations حسب Ewan R. Pearson, Isabelle Flechtner, Pål R. Njølstad, Maciej T. Małecki, Sarah E. Flanagan, Brian Larkin, Frances M. Ashcroft, I Klimeś, Ethel Codner, Violeta Iotova, Annabelle S. Slingerland, Julian Hamilton‐Shield, Jean‐Jacques Robert, Jens J. Holst, Penny Clark, Sian Ellard, Oddmund Søvik, Michel Polak, Andrew T. Hattersley

    منشور في 2006
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    Artigo
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  18. 18
    Wolcott-Rallison Syndrome

    Wolcott-Rallison Syndrome حسب Valérie Senée, Krishna M. Vattem, Marc Delépine, Lynn A. Rainbow, Céline Haton, Annick Lecoq, Nick J. Shaw, Jean-Jacques Robert, Raoul Rooman, C. Diatloff‐Zito, Jacques L. Michaud, Bassan Bin-Abbas, Doris Taha, B. Zabel, Piergiorgio Franceschini, Ali Kemal Topaloğlu, G.M. Lathrop, Timothy Barrett, Marc Nicolino, Ronald C. Wek, Cécile Julier

    منشور في 2004
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    Artigo
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  19. 19
    Metabolic outcomes in young children with type 1 diabetes differ between treatment centers: the Hvidoere Study in Young Children 2009

    Metabolic outcomes in young children with type 1 diabetes differ between treatment centers: the Hvidoere Study in Young Children 2009 حسب Carine de Beaufort, Karin Lange, Peter G.F. Swift, Jan Åman, Fergus Cameron, Luís Castaño, Harry Dorchy, Lynda K. Fisher, Hilary Hoey, Jaakko Kaprio, Mirjana Koc̆ova, Andreas Neu, Pål R. Njølstad, Moshe Phillip, Eugen J. Schoenle, Jean Jacques Robert, Tatsuhiko Urukami, Maurizio Vanelli, Thomas Danne, Timothy Barrett, F Chiarelli, Henk‐Jan Aanstoot, Henrik B. Mortensen

    منشور في 2012
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  20. 20
    Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy

    Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy حسب Lionel Van Maldergem, J. Magre, T. E. Khallouf, Tobias Gedde‐Dahl, Marc Delépine, Olav Trygstad, E Seemanová, Terence Stephenson, C. Sophia Albott, F Bonńici, Vanessa R. Panz, José Luís Medina, Paula Bogalho, Fabien Huet, Salvatore Savasta, Alain Verloès, Jean‐Jacques Robert, H. Loret, Marc de Kerdanet, Nadia Tubiana‐Rufi, André Mégarbané, J. A. Maassen, Marta E. Polak, Didier Lacombe, C. Ronald Kahn, Eduardo L. V. Silveira, Francisco Homero D’Abronzo, Florin Grigorescu, Mark Lathrop, J. Capeau, Stephen O’Rahilly

    منشور في 2002
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