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 (41-50 of 121) with videos related to

Pageof 13
Sort By:
Arthritis and Rheumatism|October 18, 2002
Reduced MEFV messenger RNA expression in patients with familial Mediterranean feverCécile Notarnicola, Marie-Noëlle Didelot, Isabelle Koné-Paut, et al.
Nucleic Acids Research|January 10, 2003
INFEVERS: the Registry for FMF and hereditary inflammatory disorders mutationsCyril Sarrauste de Menthière, Stéphane Terrière, Denis Pugnère, et al.
Nucleic Acids Research|January 10, 2003
The MetaFMF website: a high quality tool for meta-analysis of FMFDenis Pugnère, Manuel Ruiz, Cyril Sarrauste de Menthière, et al.
Orphanet Journal of Rare Diseases|October 18, 2013
The expanding spectrum of rare monogenic autoinflammatory diseasesIsabelle Touitou, Caroline Galeotti, Linda Rossi-Semerano, et al.
International Journal of Dermatology|November 16, 2018
Successful therapy with secukinumab in a patient with generalized pustular psoriasis carrying homozygous IL36RN p.His32Arg mutationRomain Gabeff, Roba Safar, Sophie Leducq, et al.
Archives of Pathology & Laboratory Medicine|June 1, 2012
NLRP7 mutation analysis in sporadic hydatidiform moles in Tunisian patients: NLRP7 and sporadic moleHanène Landolsi, Cécile Rittore, Laurent Philibert, et al.
American Journal of Medical Genetics. Part A|September 12, 2015
Confirmation of autosomal recessive inheritance of COL2A1 mutations in spondyloepiphyseal dysplasia congenita: Lessons for genetic counselingMouna Barat-Houari, Geneviève Baujat, Frédéric Tran Mau Them, et al.
Autoimmunity Reviews|September 4, 2014
Adult onset Still's disease (AOSD) in the era of biologic therapies: dichotomous view for cytokine and clinical expressionsAlexandre Thibault Jacques Maria, Alain Le Quellec, Christian Jorgensen, et al.
Human Mutation|October 8, 2015
Mutation Update for COL2A1 Gene Variants Associated with Type II CollagenopathiesMouna Barat-Houari, Guillaume Sarrabay, Vincent Gatinois, et al.
The Journal of Rheumatology|August 4, 2012
Blau arteritis resembling Takayasu disease with a novel NOD2 mutationRaju P Khubchandani, Rachana Hasija, Isabelle Touitou, et al.
Pageof 13

Showing results (41-50 of 121) with videos related to

Sort By:
Pageof 13
Arthritis and Rheumatism|October 18, 2002
Reduced MEFV messenger RNA expression in patients with familial Mediterranean feverCécile Notarnicola, Marie-Noëlle Didelot, Isabelle Koné-Paut, et al.
Nucleic Acids Research|January 10, 2003
INFEVERS: the Registry for FMF and hereditary inflammatory disorders mutationsCyril Sarrauste de Menthière, Stéphane Terrière, Denis Pugnère, et al.
Nucleic Acids Research|January 10, 2003
The MetaFMF website: a high quality tool for meta-analysis of FMFDenis Pugnère, Manuel Ruiz, Cyril Sarrauste de Menthière, et al.
Orphanet Journal of Rare Diseases|October 18, 2013
The expanding spectrum of rare monogenic autoinflammatory diseasesIsabelle Touitou, Caroline Galeotti, Linda Rossi-Semerano, et al.
International Journal of Dermatology|November 16, 2018
Successful therapy with secukinumab in a patient with generalized pustular psoriasis carrying homozygous IL36RN p.His32Arg mutationRomain Gabeff, Roba Safar, Sophie Leducq, et al.
Archives of Pathology & Laboratory Medicine|June 1, 2012
NLRP7 mutation analysis in sporadic hydatidiform moles in Tunisian patients: NLRP7 and sporadic moleHanène Landolsi, Cécile Rittore, Laurent Philibert, et al.
American Journal of Medical Genetics. Part A|September 12, 2015
Confirmation of autosomal recessive inheritance of COL2A1 mutations in spondyloepiphyseal dysplasia congenita: Lessons for genetic counselingMouna Barat-Houari, Geneviève Baujat, Frédéric Tran Mau Them, et al.
Autoimmunity Reviews|September 4, 2014
Adult onset Still's disease (AOSD) in the era of biologic therapies: dichotomous view for cytokine and clinical expressionsAlexandre Thibault Jacques Maria, Alain Le Quellec, Christian Jorgensen, et al.
Human Mutation|October 8, 2015
Mutation Update for COL2A1 Gene Variants Associated with Type II CollagenopathiesMouna Barat-Houari, Guillaume Sarrabay, Vincent Gatinois, et al.
The Journal of Rheumatology|August 4, 2012
Blau arteritis resembling Takayasu disease with a novel NOD2 mutationRaju P Khubchandani, Rachana Hasija, Isabelle Touitou, et al.
Pageof 13