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Marc Delpech

Showing results (21-30 of 39) with videos related to

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Kidney International|February 19, 2002
Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French familySophie Valleix, Séverine Drunat, Jean-Baptiste Philit, et al.
Annales De Biologie Clinique|January 25, 2023
Medical biology in France: evolution and issuesDominique Bonnefont-Rousselot, Marc Delpech, Philippe Chatron, et al.
The Journal of Rheumatology|April 1, 2005
Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndromeVéronique Hentgen, Véronique Despert, Anne-Claire Leprêtre, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndromeChrystel Leroy, Corinne Fouveaut, Sandrine Leclercq, et al.
Annales De Biologie Clinique|August 30, 2018
[Medical biology in the face of the evolution of health care needs]Claude Dreux, François-Xavier Maquart, Dominique Bonnefont-Rousselot, et al.
Digestive Diseases and Sciences|June 16, 2007
Analysis of the NOD2/CARD15 gene in patients affected with the aseptic abscesses syndrome with or without inflammatory bowel diseaseMarc François Jean André, Olivier Aumaître, Jean-Charles Piette, et al.
Gastroenterology|October 3, 2002
A family with gastrointestinal amyloidosis associated with variant lysozymeBrigitte Granel, Jacques Serratrice, Sophie Valleix, et al.
Molecular Vision|May 28, 2011
Genotype-phenotype correlations of TGFBI p.Leu509Pro, p.Leu509Arg, p.Val613Gly, and the allelic association of p.Met502Val-p.Arg555Gln mutationsFlorence Niel-Butschi, Bernadette Kantelip, Justyna Iwaszkiewicz, et al.
Arthritis and Rheumatism|September 5, 2002
The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndromeCatherine Dodé, Marc André, Thierry Bienvenu, et al.
Digestive Diseases and Sciences|September 5, 2009
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 patientsMarc F J André, Olivier Aumaître, Gilles Grateau, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Kidney International|February 19, 2002
Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French familySophie Valleix, Séverine Drunat, Jean-Baptiste Philit, et al.
Annales De Biologie Clinique|January 25, 2023
Medical biology in France: evolution and issuesDominique Bonnefont-Rousselot, Marc Delpech, Philippe Chatron, et al.
The Journal of Rheumatology|April 1, 2005
Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndromeVéronique Hentgen, Véronique Despert, Anne-Claire Leprêtre, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndromeChrystel Leroy, Corinne Fouveaut, Sandrine Leclercq, et al.
Annales De Biologie Clinique|August 30, 2018
[Medical biology in the face of the evolution of health care needs]Claude Dreux, François-Xavier Maquart, Dominique Bonnefont-Rousselot, et al.
Digestive Diseases and Sciences|June 16, 2007
Analysis of the NOD2/CARD15 gene in patients affected with the aseptic abscesses syndrome with or without inflammatory bowel diseaseMarc François Jean André, Olivier Aumaître, Jean-Charles Piette, et al.
Gastroenterology|October 3, 2002
A family with gastrointestinal amyloidosis associated with variant lysozymeBrigitte Granel, Jacques Serratrice, Sophie Valleix, et al.
Molecular Vision|May 28, 2011
Genotype-phenotype correlations of TGFBI p.Leu509Pro, p.Leu509Arg, p.Val613Gly, and the allelic association of p.Met502Val-p.Arg555Gln mutationsFlorence Niel-Butschi, Bernadette Kantelip, Justyna Iwaszkiewicz, et al.
Arthritis and Rheumatism|September 5, 2002
The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndromeCatherine Dodé, Marc André, Thierry Bienvenu, et al.
Digestive Diseases and Sciences|September 5, 2009
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 patientsMarc F J André, Olivier Aumaître, Gilles Grateau, et al.
Pageof 4