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ArticlesPeer ReviewedFull Text
Monitoring Bacterial Community of Human Gut Microbiota Reveals an Increase in Lactobacillus in Obese Patients and Methanogens in Anorexic Patients
Author / Creator:Armougom, Fabrice ; Henry, Mireille ; Vialettes, Bernard ; Raccah, Denis ; Raoult, Didier
Publisher:United States: Public Library of Science
Journal title:PloS one, 2009-09, Vol.4 (9), p.e7125-e7125
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Development and Validation of a Microarray for the Investigation of the CAZymes Encoded by the Human Gut Microbiome
Author / Creator:El Kaoutari, Abdessamad ; Armougom, Fabrice ; Leroy, Quentin ; Vialettes, Bernard ; Million, Matthieu ; Raoult, Didier ; Henrissat, Bernard
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-12, Vol.8 (12), p.e84033
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Pulmonary autoimmunity as a feature of autoimmune polyendocrine syndrome type 1 and identification of KCNRG as a bronchial autoantigen
Author / Creator:Alimohammadi, Mohammad ; Dubois, Noémie ; Sköldberg, Filip ; Hallgren, Åsa ; Tardivel, Isabelle ; Hedstrand, Håkan ; Haavik, Jan ; Husebye, Eystein S ; Gustafsson, Jan ; Rorsman, Fredrik ; Meloni, Antonella ; Janson, Christer ; Vialettes, Bernard ; Kajosaari, Merja ; Egner, William ; Sargur, Ravishankar ; Pontén, Fredrik ; Amoura, Zahir ; Grimfeld, Alain ; De Luca, Filippo ; Betterle, Corrado ; Perheentupa, Jaakko ; Kämpe, Olle ; Carel, Jean-Claude
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2009-03, Vol.106 (11), p.4396-4401
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Brain anomalies in maternally inherited diabetes and deafness syndrome
Author / Creator:Fromont, I. ; Nicoli, F. ; Valéro, R. ; Felician, O. ; Lebail, B. ; Lefur, Y. ; Mancini, J. ; Paquis-Flucklinger, V. ; Cozzone, P. J. ; Vialettes, Bernard
Publisher:Heidelberg: D. Steinkopff-Verlag
Journal title:Journal of neurology, 2009-10, Vol.256 (10), p.1696-1704
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Unacylated Ghrelin is associated with the isolated low HDL-cholesterol obese phenotype independently of insulin resistance and CRP level
Author / Creator:Nogueira, Juan-Patricio ; Maraninchi, Marie ; Béliard, Sophie ; Lorec, Anne Marie ; Berthet, Bruno ; Bégu-Le Corroller, Audrey ; Dubois, Noémie ; Grangeot, Rachel ; Mattei, Catherine ; Gaudart, Jean ; Nicolay, Alain ; Portugal, Henri ; Vialettes, Bernard ; Valéro, René
Publisher:England: BioMed Central Ltd
Journal title:Nutrition & metabolism, 2012-03, Vol.9 (1), p.17-407, Article 17
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Intronic mutations outside of Alu -repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia
Author / Creator:Amsellem, Sabine ; Briffaut, Dorothée ; Carrié, Alain ; Rabès, Jean ; Girardet, Jean ; Fredenrich, Alexandre ; Moulin, Philippe ; Krempf, Michel ; Reznik, Yves ; Vialettes, Bernard ; de Gennes, Jean ; Brukert, Eric ; Benlian, Pascale
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2002-12, Vol.111 (6), p.501-510
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Microvascular Diabetes Complications in Wolfram Syndrome (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness [DIDMOAD])
Author / Creator:Cano, Aline ; Molines, Laurent ; Valéro, René ; Simonin, Gilbert ; Paquis-Flucklinger, Véronique ; Vialettes, Bernard
Publisher:American Diabetes Association
Journal title:Diabetes care, 2007-09, Vol.30 (9), p.2327-2330
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Acute Hyperinsulinism Modulates Plasma Apolipoprotein B-48 Triglyceride—Rich Lipoproteins in Healthy Subjects During the Postprandial Period
Author / Creator:Harbis, A. ; Defoort, C. ; Narbonne, H. ; Juhel, C. ; Senft, M. ; Latge, C. ; Delenne, B. ; Portugal, H. ; Atlan-Gepner, C. ; Vialettes, B. ; Lairon, D.
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2001-02, Vol.50 (2), p.462-469
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Comment on: Greenbaum et al. Through the Fog: Recent Clinical Trials to Preserve β-Cell Function in Type 1 Diabetes. Diabetes 2012;61:1323–1330
Author / Creator:Vialettes, Bernard ; Valéro, René
Publisher:United States: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2012-12, Vol.61 (12), p.e18-e18
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Wolfram syndrome in French population: Characterization of novel mutations and polymorphisms in theWFS1 gene
Author / Creator:Giuliano, Fabienne ; Bannwarth, Sylvie ; Monnot, Sophie ; Cano, Aline ; Chabrol, Brigitte ; Vialettes, Bernard ; Delobel, Bruno ; Paquis-Flucklinger, Veronique
Journal title:Human mutation, 2005-01, Vol.25 (1), p.99-100
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No Association Between lck Gene Polymorphisms and Protein Level in Type 1 Diabetes
Author / Creator:Nervi, Solange ; Nicodeme, Sandra ; Gartioux, Corinne ; Atlan, Catherine ; Lathrop, Marc ; Reviron, Denis ; Naquet, Philippe ; Matsuda, Fumihiko ; Imbert, Jean ; Vialettes, Bernard
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2002-11, Vol.51 (11), p.3326-3330
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Pancreatic Regenerating Gene Overexpression in the Nonobese Diabetic Mouse During Active Diabetogenesis
Author / Creator:Baeza, Nathalie J ; Moriscot, Christine I ; Renaud, Wanda P ; Okamoto, Hiroshi ; Figarella, Catherine G ; Vialettes, Bernard H
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 1996-01, Vol.45 (1), p.67-70
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ArticlesPeer ReviewedFull Text
Point-of-Care Measurements of HbA1c: Simplicity Does Not Mean Laxity With Controls
Author / Creator:Leca, Viviane ; Ibrahim, Zouher ; Lombard-Pontou, Elise ; Maraninchi, Marie ; Guieu, Régis ; Portugal, Henri ; Valéro, René ; Vialettes, Bernard
Publisher:American Diabetes Association
Journal title:Diabetes care, 2012-12, Vol.35 (12), p.e85-e85
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Point-of-care measurements of HbA(1c): simplicity does not mean laxity with controls
Author / Creator:Leca, Viviane ; Ibrahim, Zouher ; Lombard-Pontou, Elise ; Maraninchi, Marie ; Guieu, Régis ; Portugal, Henri ; Valéro, René ; Vialettes, Bernard
Publisher:United States
Journal title:Diabetes care, 2012-12, Vol.35 (12), p.e85-e85
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ArticlesPeer ReviewedFull Text
Novel Unstable Mutation in Mitochondrial DNA Responsible for Maternally Inherited Diabetes and Deafness
Author / Creator:Bannwarth, Sylvie ; Abbassi, Meriame ; Valéro, René ; Fragaki, Konstantina ; Dubois, Noémie ; Vialettes, Bernard ; Paquis-Flucklinger, Véronique
Publisher:United States: American Diabetes Association
Journal title:Diabetes care, 2011-12, Vol.34 (12), p.2591-2593
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Growth hormone level at admission and its evolution during refeeding are predictive of short-term outcome in restrictive anorexia nervosa
Author / Creator:Nogueira, Juan P. ; Valéro, René ; Maraninchi, Marie ; Lorec, Anne M. ; Samuelian-Massat, Catherine ; Bégu-Le Corroller, Audrey ; Nicolay, Alain ; Gaudart, Jean ; Portugal, Henri ; Vialettes, Bernard
Publisher:Cambridge, UK: Cambridge University Press
Journal title:British journal of nutrition, 2013-06, Vol.109 (12), p.2175-2181
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A Novel Unstable Mutation in Mitochondrial DNA Responsibly for Maternally Inherited Diabetes and Deafness
Author / Creator:BANNWARTH, Sylvie ; ABBASSI, Meriame ; VALERO, Rene ; FRAGAKI, Konstantina ; DUBOIS, Noémie ; VIALETTES, Bernard ; PAQUIS-FLUCKLINGER, Véronique
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2011, Vol.34 (12), p.2591-2593
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ArticlesPeer ReviewedFull Text
Wolfram syndrome in French population: Characterization of novel mutations and polymorphisms in the WFS1 gene
Author / Creator:Giuliano, Fabienne ; Bannwarth, Sylvie ; Monnot, Sophie ; Cano, Aline ; Chabrol, Brigitte ; Vialettes, Bernard ; Delobel, Bruno ; Paquis-Flucklinger, Veronique
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2005-01, Vol.25 (1), p.99-100
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ArticlesPeer ReviewedFull Text
Microvascular Diabetes Complications in Wolfram Syndrome (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness [DIDMOAD]): An age- and duration-matched comparison with common type 1 diab...
Author / Creator:Cano, Aline ; Molines, Laurent ; Valéro, René ; Simonin, Gilbert ; Paquis-Flucklinger, Véronique ; Vialettes, Bernard
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2007-09, Vol.30 (9), p.2327-2330
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ArticlesPeer ReviewedFull Text
Development and Validation of a Microarray for the Investigation of the CAZymes Encoded by the Human Gut Microbiome: e84033
Author / Creator:Kaoutari, Abdessamad El ; Armougom, Fabrice ; Leroy, Quentin ; Vialettes, Bernard ; Million, Matthieu ; Raoult, Didier ; Henrissat, Bernard
Journal title:PloS one, 2013-12, Vol.8 (12)
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Monitoring Bacterial Community of Human Gut Microbiota Reveals an Increase in Lactobacillus in Obese Patients and Methanogens in Anorexic Patients

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Development and Validation of a Microarray for the Investigation of the CAZymes Encoded by the Human Gut Microbiome

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Pulmonary autoimmunity as a feature of autoimmune polyendocrine syndrome type 1 and identification of KCNRG as a bronchial autoantigen

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Brain anomalies in maternally inherited diabetes and deafness syndrome

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Unacylated Ghrelin is associated with the isolated low HDL-cholesterol obese phenotype independently of insulin resistance and CRP level

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Intronic mutations outside of Alu -repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia

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Microvascular Diabetes Complications in Wolfram Syndrome (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness [DIDMOAD])

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Acute Hyperinsulinism Modulates Plasma Apolipoprotein B-48 Triglyceride—Rich Lipoproteins in Healthy Subjects During the Postprandial Period

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Comment on: Greenbaum et al. Through the Fog: Recent Clinical Trials to Preserve β-Cell Function in Type 1 Diabetes. Diabetes 2012;61:1323–1330

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Wolfram syndrome in French population: Characterization of novel mutations and polymorphisms in theWFS1 gene

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No Association Between lck Gene Polymorphisms and Protein Level in Type 1 Diabetes

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Pancreatic Regenerating Gene Overexpression in the Nonobese Diabetic Mouse During Active Diabetogenesis

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Point-of-Care Measurements of HbA1c: Simplicity Does Not Mean Laxity With Controls

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Point-of-care measurements of HbA(1c): simplicity does not mean laxity with controls

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Novel Unstable Mutation in Mitochondrial DNA Responsible for Maternally Inherited Diabetes and Deafness

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Growth hormone level at admission and its evolution during refeeding are predictive of short-term outcome in restrictive anorexia nervosa

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A Novel Unstable Mutation in Mitochondrial DNA Responsibly for Maternally Inherited Diabetes and Deafness

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Wolfram syndrome in French population: Characterization of novel mutations and polymorphisms in the WFS1 gene

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Microvascular Diabetes Complications in Wolfram Syndrome (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness [DIDMOAD]): An age- and duration-matched comparison with common type 1 diab...

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Development and Validation of a Microarray for the Investigation of the CAZymes Encoded by the Human Gut Microbiome: e84033

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