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Marc Delpech

Showing results (11-20 of 39) with videos related to

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Comptes Rendus Biologies|January 28, 2006
Prevalence and distribution of MEFV mutations among Arabs from the Maghreb patients suffering from familial Mediterranean feverLatifa Belmahi, Abdelaziz Sefiani, Corinne Fouveau, et al.
Molecular Vision|July 9, 2011
A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular featuresAntoine P Brézin, Brigitte Nedelec, Amandine Barjol, et al.
American Journal of Human Genetics|July 11, 2006
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humansSophie Valleix, Florence Niel, Brigitte Nedelec, et al.
Biophysical Journal|July 20, 2011
Synchrotron x-ray microdiffraction reveals intrinsic structural features of amyloid deposits in situFatma Briki, Jérôme Vérine, Jean Doucet, et al.
Investigative Ophthalmology & Visual Science|December 31, 2005
H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD familySophie Valleix, Brigitte Nedelec, Florence Rigaudiere, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 1, 2003
Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French familyNadine Magy, Sophie Valleix, Gilles Grateau, et al.
Investigative Ophthalmology & Visual Science|June 26, 2003
Truncating mutations in the carbohydrate sulfotransferase 6 gene (CHST6) result in macular corneal dystrophyFlorence Niel, Pierre Ellies, Paul Dighiero, et al.
Current Drug Targets. Inflammation and Allergy|February 22, 2005
Amyloidosis and auto-inflammatory syndromesGilles Grateau, Isabelle Jéru, Saad Rouaghe, et al.
Arthritis and Rheumatism|February 5, 2005
Association of the R92Q TNFRSF1A mutation and extracranial deep vein thrombosis in patients with Behçet's diseaseZahir Amoura, Catherine Dodé, Sophie Hue, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 10, 2002
Mutational spectrum in the MEFV and TNFRSF1A genes in patients suffering from AA amyloidosis and recurrent inflammatory attacksCatherine Dodé, Bouke P C Hazenberg, Christophe Pêcheux, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Comptes Rendus Biologies|January 28, 2006
Prevalence and distribution of MEFV mutations among Arabs from the Maghreb patients suffering from familial Mediterranean feverLatifa Belmahi, Abdelaziz Sefiani, Corinne Fouveau, et al.
Molecular Vision|July 9, 2011
A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular featuresAntoine P Brézin, Brigitte Nedelec, Amandine Barjol, et al.
American Journal of Human Genetics|July 11, 2006
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humansSophie Valleix, Florence Niel, Brigitte Nedelec, et al.
Biophysical Journal|July 20, 2011
Synchrotron x-ray microdiffraction reveals intrinsic structural features of amyloid deposits in situFatma Briki, Jérôme Vérine, Jean Doucet, et al.
Investigative Ophthalmology & Visual Science|December 31, 2005
H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD familySophie Valleix, Brigitte Nedelec, Florence Rigaudiere, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 1, 2003
Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French familyNadine Magy, Sophie Valleix, Gilles Grateau, et al.
Investigative Ophthalmology & Visual Science|June 26, 2003
Truncating mutations in the carbohydrate sulfotransferase 6 gene (CHST6) result in macular corneal dystrophyFlorence Niel, Pierre Ellies, Paul Dighiero, et al.
Current Drug Targets. Inflammation and Allergy|February 22, 2005
Amyloidosis and auto-inflammatory syndromesGilles Grateau, Isabelle Jéru, Saad Rouaghe, et al.
Arthritis and Rheumatism|February 5, 2005
Association of the R92Q TNFRSF1A mutation and extracranial deep vein thrombosis in patients with Behçet's diseaseZahir Amoura, Catherine Dodé, Sophie Hue, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 10, 2002
Mutational spectrum in the MEFV and TNFRSF1A genes in patients suffering from AA amyloidosis and recurrent inflammatory attacksCatherine Dodé, Bouke P C Hazenberg, Christophe Pêcheux, et al.
Pageof 4