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 (51-60 of 121) with videos related to

Pageof 13
Sort By:
Rheumatology (Oxford, England)|May 26, 2009
The clinical spectrum of 94 patients carrying a single mutated MEFV alleleIsabelle Koné-Paut, Véronique Hentgen, Severine Guillaume-Czitrom, et al.
Annals of the Rheumatic Diseases|March 18, 2018
'A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease'Florian Berteau, Bénédicte Rouvière, Alice Nau, et al.
European Journal of Human Genetics : EJHG|June 13, 2019
Current practices for the genetic diagnosis of autoinflammatory diseases: results of a European Molecular Genetics Quality Network SurveyDorota Rowczenio, Yael Shinar, Isabella Ceccherini, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 29, 2011
The spectrum of NLRP7 mutations in French patients with recurrent hydatidiform moleJoël Muhlstein, François Golfier, Cécile Rittore, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|May 31, 2011
Screening for NLRP7 mutations in familial and sporadic recurrent hydatidiform moles: report of 2 Tunisian familiesHanène Landolsi, Cécile Rittore, Laurent Philibert, et al.
Joint Bone Spine|January 28, 2014
TNFRII polymorphism is associated with response to TNF blockers in rheumatoid arthritis patients seronegative for ACPAYves-Marie Pers, Doris Cadart, Cécile Rittore, et al.
Annals of the Rheumatic Diseases|August 14, 2018
Consensus proposal for taxonomy and definition of the autoinflammatory diseases (AIDs): a Delphi studyEldad Ben-Chetrit, Marco Gattorno, Ahmet Gul, et al.
Autoimmunity Reviews|June 12, 2018
Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literatureFlorian Berteau, Bénédicte Rouviere, Aurélien Delluc, et al.
Human Mutation|July 17, 2022
Biallelic NLRP7 variants in patients with recurrent hydatidiform mole: A review and expert consensusRima Slim, Rosemary Fisher, Florian Milhavet, et al.
Genetics Research International|January 4, 2014
Lack of TEK Gene Mutation in Patients with Cutaneomucosal Venous Malformations from the North-Western Region of AlgeriaNabila Brahami, Mourad Aribi, Badr-Eddine Sari, et al.
Pageof 13

Showing results (51-60 of 121) with videos related to

Sort By:
Pageof 13
Rheumatology (Oxford, England)|May 26, 2009
The clinical spectrum of 94 patients carrying a single mutated MEFV alleleIsabelle Koné-Paut, Véronique Hentgen, Severine Guillaume-Czitrom, et al.
Annals of the Rheumatic Diseases|March 18, 2018
'A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease'Florian Berteau, Bénédicte Rouvière, Alice Nau, et al.
European Journal of Human Genetics : EJHG|June 13, 2019
Current practices for the genetic diagnosis of autoinflammatory diseases: results of a European Molecular Genetics Quality Network SurveyDorota Rowczenio, Yael Shinar, Isabella Ceccherini, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 29, 2011
The spectrum of NLRP7 mutations in French patients with recurrent hydatidiform moleJoël Muhlstein, François Golfier, Cécile Rittore, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|May 31, 2011
Screening for NLRP7 mutations in familial and sporadic recurrent hydatidiform moles: report of 2 Tunisian familiesHanène Landolsi, Cécile Rittore, Laurent Philibert, et al.
Joint Bone Spine|January 28, 2014
TNFRII polymorphism is associated with response to TNF blockers in rheumatoid arthritis patients seronegative for ACPAYves-Marie Pers, Doris Cadart, Cécile Rittore, et al.
Annals of the Rheumatic Diseases|August 14, 2018
Consensus proposal for taxonomy and definition of the autoinflammatory diseases (AIDs): a Delphi studyEldad Ben-Chetrit, Marco Gattorno, Ahmet Gul, et al.
Autoimmunity Reviews|June 12, 2018
Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literatureFlorian Berteau, Bénédicte Rouviere, Aurélien Delluc, et al.
Human Mutation|July 17, 2022
Biallelic NLRP7 variants in patients with recurrent hydatidiform mole: A review and expert consensusRima Slim, Rosemary Fisher, Florian Milhavet, et al.
Genetics Research International|January 4, 2014
Lack of TEK Gene Mutation in Patients with Cutaneomucosal Venous Malformations from the North-Western Region of AlgeriaNabila Brahami, Mourad Aribi, Badr-Eddine Sari, et al.
Pageof 13