Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Isabelle Touitou

Showing results (61-70 of 121) with videos related to

Pageof 13
Sort By:
Orphanet Journal of Rare Diseases|March 12, 2015
Tolerance and efficacy of off-label anti-interleukin-1 treatments in France: a nationwide surveyLinda Rossi-Semerano, Bruno Fautrel, Daniel Wendling, et al.
Frontiers in Immunology|October 24, 2013
Association Analysis of IL10, TNF-α, and IL23R-IL12RB2 SNPs with Behçet's Disease Risk in Western AlgeriaOuahiba Khaib Dit Naib, Mourad Aribi, Aicha Idder, et al.
Plos One|December 3, 2010
Combined mutation and rearrangement screening by quantitative PCR high-resolution melting: is it relevant for hereditary recurrent Fever genes?Nathalie Pallares-Ruiz, Laurent Philibert, Bruno Dumont, et al.
European Journal of Dermatology : EJD|December 6, 2018
Chronic leg ulcer revealing adenosine deaminase 2 deficiency: an atypical presentationHélène Martin, Anne-Claire Bursztejn, Jean-Francois Cuny, et al.
Mediators of Inflammation|April 30, 2014
Circulating miRNA-125b is a potential biomarker predicting response to rituximab in rheumatoid arthritisIsabelle Duroux-Richard, Yves-Marie Pers, Sylvie Fabre, et al.
Annals of the Rheumatic Diseases|March 19, 2013
Identification of a new exon 2-skipped TNFR1 transcript: regulation by three functional polymorphisms of the TNFR-associated periodic syndrome (TRAPS) geneCécile Rittore, Elodie Sanchez, Stephan Soler, et al.
Joint Bone Spine|July 3, 2016
Association of TRAF1-C5 with risk of uveitis in juvenile idiopathic arthritisYves-Marie Pers, Pierre Le Blay, Catherine Ludwig, et al.
Annals of the Rheumatic Diseases|April 22, 2018
Large deletion in 6q associated to A20 haploinsufficiency and thoracoabdominal heterotaxySébastien Viel, Elodie Cheyssac, Rémi Pescarmona, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Familial Mediterranean fever is no longer a rare disease in ItalyMicaela La Regina, Gabriella Nucera, Marialuisa Diaco, et al.
Human Reproduction Update|May 30, 2020
C-reactive protein and ART outcomes: a systematic reviewSophie Brouillet, Guilaine Boursier, Margaux Anav, et al.
Pageof 13

Showing results (61-70 of 121) with videos related to

Sort By:
Pageof 13
Orphanet Journal of Rare Diseases|March 12, 2015
Tolerance and efficacy of off-label anti-interleukin-1 treatments in France: a nationwide surveyLinda Rossi-Semerano, Bruno Fautrel, Daniel Wendling, et al.
Frontiers in Immunology|October 24, 2013
Association Analysis of IL10, TNF-α, and IL23R-IL12RB2 SNPs with Behçet's Disease Risk in Western AlgeriaOuahiba Khaib Dit Naib, Mourad Aribi, Aicha Idder, et al.
Plos One|December 3, 2010
Combined mutation and rearrangement screening by quantitative PCR high-resolution melting: is it relevant for hereditary recurrent Fever genes?Nathalie Pallares-Ruiz, Laurent Philibert, Bruno Dumont, et al.
European Journal of Dermatology : EJD|December 6, 2018
Chronic leg ulcer revealing adenosine deaminase 2 deficiency: an atypical presentationHélène Martin, Anne-Claire Bursztejn, Jean-Francois Cuny, et al.
Mediators of Inflammation|April 30, 2014
Circulating miRNA-125b is a potential biomarker predicting response to rituximab in rheumatoid arthritisIsabelle Duroux-Richard, Yves-Marie Pers, Sylvie Fabre, et al.
Annals of the Rheumatic Diseases|March 19, 2013
Identification of a new exon 2-skipped TNFR1 transcript: regulation by three functional polymorphisms of the TNFR-associated periodic syndrome (TRAPS) geneCécile Rittore, Elodie Sanchez, Stephan Soler, et al.
Joint Bone Spine|July 3, 2016
Association of TRAF1-C5 with risk of uveitis in juvenile idiopathic arthritisYves-Marie Pers, Pierre Le Blay, Catherine Ludwig, et al.
Annals of the Rheumatic Diseases|April 22, 2018
Large deletion in 6q associated to A20 haploinsufficiency and thoracoabdominal heterotaxySébastien Viel, Elodie Cheyssac, Rémi Pescarmona, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
Familial Mediterranean fever is no longer a rare disease in ItalyMicaela La Regina, Gabriella Nucera, Marialuisa Diaco, et al.
Human Reproduction Update|May 30, 2020
C-reactive protein and ART outcomes: a systematic reviewSophie Brouillet, Guilaine Boursier, Margaux Anav, et al.
Pageof 13