Publications by authors named "Marc Delpech"

Claim this Profile
[
[Medical biology in France: evolution and issues].
Dominique Bonnefont-Rousselot, Marc Delpech, Philippe Chatron, Jean-Louis Gueant, Yves Le Bouc

Ann Biol Clin (Paris)· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Medical biology in the face of the evolution of health care needs].
Claude Dreux, François-Xavier Maquart, Dominique Bonnefont-Rousselot, Marc Delpech, Jean-Louis Gueant

Ann Biol Clin (Paris)· October 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[2018 should be a very good year for SFBC, the year of a renewal].
Marc Delpech

Ann Biol Clin (Paris)· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
VLITL is a major cross-β-sheet signal for fibrinogen Aα-chain frameshift variants.
Cyrille Garnier, Fatma Briki, Brigitte Nedelec, Patrick Le Pogamp, Ahmet Dogan, Marc Delpech

Blood· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Reform of the outside nomenclature biomedical tests in France: a two year review.
Katell Peoc'h, Sylvain Lehmann, Marc Delpech

Ann Biol Clin (Paris)· August 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Laboratory medicine and POCT: an appointment not to be missed!
Marc Delpech, Joëlle Goudable, Michel Vaubourdolle

Ann Biol Clin (Paris)· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profile.
Sophie Valleix, Guglielmo Verona, Noémie Jourde-Chiche, Brigitte Nédelec, P Patrizia Mangione, Marc Delpech

Nat Commun· January 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Next generation sequencing on patients with LGMD and nonspecific myopathies: Findings associated with ANO5 mutations.
Marco Savarese, Giuseppina Di Fruscio, Giorgio Tasca, Lucia Ruggiero, Sandra Janssens, Marc Delpech

Neuromuscul Disord· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Amyloid polyneuropathies--biochemical and genetic aspects].
Marc Delpech, Sophie Valleix

Bull Acad Natl Med· October 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin.
Sophie Valleix, Julian D Gillmore, Frank Bridoux, Palma P Mangione, Ahmet Dogan, Marc Delpech

N Engl J Med· June 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular features.
Antoine P Brézin, Brigitte Nedelec, Amandine Barjol, Pierre-Raphael Rothschild, Marc Delpech

Mol Vis· November 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotype-phenotype correlations of TGFBI p.Leu509Pro, p.Leu509Arg, p.Val613Gly, and the allelic association of p.Met502Val-p.Arg555Gln mutations.
Florence Niel-Butschi, Bernadette Kantelip, Justyna Iwaszkiewicz, Vincent Zoete, Mathieu Boimard, Marc Delpech

Mol Vis· September 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Synchrotron x-ray microdiffraction reveals intrinsic structural features of amyloid deposits in situ.
Fatma Briki, Jérôme Vérine, Jean Doucet, Philippe Bénas, Barbara Fayard, Marc Delpech

Biophys J· July 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Longest form of CCTG microsatellite repeat in the promoter of the CD2BP1/PSTPIP1 gene is associated with aseptic abscesses and with Crohn disease in French patients.
Marc F J André, Olivier Aumaître, Gilles Grateau, Mathias Chamaillard, Nathalie Costedoat-Chalumeau, Marc Delpech

Dig Dis Sci· June 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[From hereditary recurrent fevers to autoinflammatory syndromes: the contribution of genetics].
Marc Delpech

Bull Acad Natl Med· November 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome.
Chrystel Leroy, Corinne Fouveaut, Sandrine Leclercq, Sébastien Jacquemont, Hélène Du Boullay, Marc Delpech

Eur J Hum Genet· July 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Analysis of the NOD2/CARD15 gene in patients affected with the aseptic abscesses syndrome with or without inflammatory bowel disease.
Marc François Jean André, Olivier Aumaître, Jean-Charles Piette, Gilles Grateau, Marie-Céleste Cardoso, Marc Delpech

Dig Dis Sci· February 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis.
Catherine Dodé, Corinne Fouveaut, Geert Mortier, Sandra Janssens, Jérôme Bertherat, Marc Delpech

Hum Mutat· January 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
K
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.
Catherine Dodé, Luis Teixeira, Jacqueline Levilliers, Corinne Fouveaut, Philippe Bouchard, Marc Delpech

PLoS Genet· October 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.
Sophie Valleix, Florence Niel, Brigitte Nedelec, Marie-Paule Algros, Claire Schwartz, Marc Delpech

Am J Hum Genet· August 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prevalence and distribution of MEFV mutations among Arabs from the Maghreb patients suffering from familial Mediterranean fever.
Latifa Belmahi, Abdelaziz Sefiani, Corinne Fouveau, Josué Feingold, Marc Delpech

C R Biol· February 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family.
Sophie Valleix, Brigitte Nedelec, Florence Rigaudiere, Paul Dighiero, Yves Pouliquen, Marc Delpech

Invest Ophthalmol Vis Sci· January 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Amyloidosis: a model of misfolded protein disorder].
Gilles Grateau, Jérôme Verine, Marc Delpech, Madeleine Ries

Med Sci (Paris)· September 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome.
Véronique Hentgen, Véronique Despert, Anne-Claire Leprêtre, Laurence Cuisset, Jacqueline Chevrant-Breton, Marc Delpech

J Rheumatol· April 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Amyloidosis and auto-inflammatory syndromes.
Gilles Grateau, Isabelle Jéru, Saad Rouaghe, Cécile Cazeneuve, Nathalie Ravet, Marc Delpech

Curr Drug Targets Inflamm Allergy· February 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis