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Bernard Grandchamp

Showing results (11-20 of 87) with videos related to

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Annals of Clinical Biochemistry|April 27, 2012
Two novel mutations in the L ferritin coding sequence associated with benign hyperferritinaemia unmasked by glycosylated ferritin assayVanessa Thurlow, Bipin Vadher, Adrian Bomford, et al.
Journal of Human Genetics|September 4, 2007
Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P geneRobert Aquaron, Nadem Soufir, Jean-Louis Bergé-Lefranc, et al.
Diabetes Care|August 29, 2006
Ferritin and transferrin are both predictive of the onset of hyperglycemia in men and women over 3 years: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) studyFrédéric Fumeron, Franck Péan, Fatti Driss, et al.
Experimental Cell Research|August 13, 2005
A physiological model to study iron recycling in macrophagesConstance Delaby, Nathalie Pilard, Gilles Hetet, et al.
Haematologica|August 18, 2010
Immunoassay for human serum hemojuvelinCarole Brasse-Lagnel, Maura Poli, Céline Lesueur, et al.
Journal of Clinical Microbiology|July 31, 2009
First description of NOD2 variant associated with defective neutrophil responses in a woman with granulomatous mastitis related to corynebacteriaBéatrice Bercot, Caroline Kannengiesser, Claire Oudin, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002
Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT)Jérĵme Lamoril, Christophe Andant, Laurent Gouya, et al.
British Journal of Haematology|January 13, 2011
Is EPO therapy able to correct iron deficiency anaemia caused by matriptase-2 deficiency?Gaël Nicolas, Jean-Christophe Deschemin, Andrew J Ramsay, et al.
Nature Genetics|December 26, 2001
The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECHLaurent Gouya, Herve Puy, Anne-Marie Robreau, et al.
Journal of Neurology|July 26, 2002
Association study between iron-related genes polymorphisms and Parkinson's diseaseClaire Borie, Francesca Gasparini, Patrice Verpillat, et al.
Pageof 9

Showing results (11-20 of 87) with videos related to

Sort By:
Pageof 9
Annals of Clinical Biochemistry|April 27, 2012
Two novel mutations in the L ferritin coding sequence associated with benign hyperferritinaemia unmasked by glycosylated ferritin assayVanessa Thurlow, Bipin Vadher, Adrian Bomford, et al.
Journal of Human Genetics|September 4, 2007
Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P geneRobert Aquaron, Nadem Soufir, Jean-Louis Bergé-Lefranc, et al.
Diabetes Care|August 29, 2006
Ferritin and transferrin are both predictive of the onset of hyperglycemia in men and women over 3 years: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) studyFrédéric Fumeron, Franck Péan, Fatti Driss, et al.
Experimental Cell Research|August 13, 2005
A physiological model to study iron recycling in macrophagesConstance Delaby, Nathalie Pilard, Gilles Hetet, et al.
Haematologica|August 18, 2010
Immunoassay for human serum hemojuvelinCarole Brasse-Lagnel, Maura Poli, Céline Lesueur, et al.
Journal of Clinical Microbiology|July 31, 2009
First description of NOD2 variant associated with defective neutrophil responses in a woman with granulomatous mastitis related to corynebacteriaBéatrice Bercot, Caroline Kannengiesser, Claire Oudin, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002
Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT)Jérĵme Lamoril, Christophe Andant, Laurent Gouya, et al.
British Journal of Haematology|January 13, 2011
Is EPO therapy able to correct iron deficiency anaemia caused by matriptase-2 deficiency?Gaël Nicolas, Jean-Christophe Deschemin, Andrew J Ramsay, et al.
Nature Genetics|December 26, 2001
The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECHLaurent Gouya, Herve Puy, Anne-Marie Robreau, et al.
Journal of Neurology|July 26, 2002
Association study between iron-related genes polymorphisms and Parkinson's diseaseClaire Borie, Francesca Gasparini, Patrice Verpillat, et al.
Pageof 9