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Metabolism: Clinical and Experimental
|
October 29, 2005
Fasting apoprotein B-48 level and coronary artery disease in a population without frank fasting hypertriglyceridemia
René Valero, Anne-Marie Lorec, Franck Paganelli, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 26, 2009
Late diagnosis of an unstable hemoglobin in a diabetic patient: Hb Baille alpha2 122(H5)His>Tyr
Nathalie Bonello-Palot, Katia Gonnet, Christophe Ducros, et al.
Human Mutation
|
December 18, 2004
Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene
Fabienne Giuliano, Sylvie Bannwarth, Sophie Monnot, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 27, 2009
Comparison of performances of various HbA1c methods in Haemoglobin Camperdown variant detection: consequences in diabetes management
Bénédicte Gaborit, Alain Nicolay, René Valéro, et al.
Diabetes Care
|
November 23, 2012
Point-of-care measurements of HbA(1c): simplicity does not mean laxity with controls
Viviane Leca, Zouher Ibrahim, Elise Lombard-Pontou, et al.
Journal of Clinical Microbiology
|
July 26, 2013
Molecular studies neglect apparently gram-negative populations in the human gut microbiota
Perrine Hugon, Jean-Christophe Lagier, Catherine Robert, et al.
Infection Control and Hospital Epidemiology
|
October 29, 2002
Disruption of services in an internal medicine unit due to a nosocomial influenza outbreak
Catherine Sartor, Christine Zandotti, Fanny Romain, et al.
Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation
|
October 4, 2005
A randomized trial of low-protein diet in type 1 and in type 2 diabetes mellitus patients with incipient and overt nephropathy
Bertrand Dussol, Cecilia Iovanna, Denis Raccah, et al.
Annales D'Endocrinologie
|
May 16, 2020
Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations
Anne-Gaëlle Decoux-Poullot, Sylvie Bannwarth, Vincent Procaccio, et al.
Diabetes
|
October 29, 2002
No association between lck gene polymorphisms and protein level in type 1 diabetes
Solange Nervi, Sandra Nicodeme, Corinne Gartioux, et al.
Page
of 4
Search research articles
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Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
Metabolism: Clinical and Experimental
|
October 29, 2005
Fasting apoprotein B-48 level and coronary artery disease in a population without frank fasting hypertriglyceridemia
René Valero, Anne-Marie Lorec, Franck Paganelli, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 26, 2009
Late diagnosis of an unstable hemoglobin in a diabetic patient: Hb Baille alpha2 122(H5)His>Tyr
Nathalie Bonello-Palot, Katia Gonnet, Christophe Ducros, et al.
Human Mutation
|
December 18, 2004
Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene
Fabienne Giuliano, Sylvie Bannwarth, Sophie Monnot, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 27, 2009
Comparison of performances of various HbA1c methods in Haemoglobin Camperdown variant detection: consequences in diabetes management
Bénédicte Gaborit, Alain Nicolay, René Valéro, et al.
Diabetes Care
|
November 23, 2012
Point-of-care measurements of HbA(1c): simplicity does not mean laxity with controls
Viviane Leca, Zouher Ibrahim, Elise Lombard-Pontou, et al.
Journal of Clinical Microbiology
|
July 26, 2013
Molecular studies neglect apparently gram-negative populations in the human gut microbiota
Perrine Hugon, Jean-Christophe Lagier, Catherine Robert, et al.
Infection Control and Hospital Epidemiology
|
October 29, 2002
Disruption of services in an internal medicine unit due to a nosocomial influenza outbreak
Catherine Sartor, Christine Zandotti, Fanny Romain, et al.
Journal of Renal Nutrition : the Official Journal of the Council on Renal Nutrition of the National Kidney Foundation
|
October 4, 2005
A randomized trial of low-protein diet in type 1 and in type 2 diabetes mellitus patients with incipient and overt nephropathy
Bertrand Dussol, Cecilia Iovanna, Denis Raccah, et al.
Annales D'Endocrinologie
|
May 16, 2020
Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations
Anne-Gaëlle Decoux-Poullot, Sylvie Bannwarth, Vincent Procaccio, et al.
Diabetes
|
October 29, 2002
No association between lck gene polymorphisms and protein level in type 1 diabetes
Solange Nervi, Sandra Nicodeme, Corinne Gartioux, et al.
Page
of 4