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

Claude Messiaen

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Orphanet Journal of Rare Diseases|January 5, 2020
Healthcare trajectory of children with rare bone disease attending pediatric emergency departmentsDavid Dawei Yang, Geneviève Baujat, Antoine Neuraz, et al.
Orphanet Journal of Rare Diseases|May 21, 2017
Management of rare diseases of the Head, Neck and Teeth: results of a French population-based prospective 8-year studyLisa Friedlander, Rémy Choquet, Eva Galliani, et al.
Orphanet Journal of Rare Diseases|July 2, 2017
Prevalence of fibrodysplasia ossificans progressiva (FOP) in France: an estimate based on a record linkage of two national databasesGeneviève Baujat, Rémy Choquet, Stéphane Bouée, et al.
Annals of the Rheumatic Diseases|December 22, 2010
A multicentre, randomised, double-blind, placebo-controlled trial with the interleukin-1 receptor antagonist anakinra in patients with systemic-onset juvenile idiopathic arthritis (ANAJIS trial)Pierre Quartier, Florence Allantaz, Rolando Cimaz, et al.
Studies in Health Technology and Informatics|September 16, 2010
CEMARA an information system for rare diseasesPaul Landais, Claude Messiaen, Ana Rath, et al.
Studies in Health Technology and Informatics|May 20, 2008
CEMARA: a Web dynamic application within a N-tier architecture for rare diseasesClaude Messiaen, Loïc Le Mignot, Ana Rath, et al.
Orphanet Journal of Rare Diseases|November 5, 2021
Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseasesWafa Kallali, Claude Messiaen, Roumaisah Saïdi, et al.
Orphanet Journal of Rare Diseases|August 5, 2021
10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in FranceClaude Messiaen, Caroline Racine, Ahlem Khatim, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Orphanet Journal of Rare Diseases|January 5, 2020
Healthcare trajectory of children with rare bone disease attending pediatric emergency departmentsDavid Dawei Yang, Geneviève Baujat, Antoine Neuraz, et al.
Orphanet Journal of Rare Diseases|May 21, 2017
Management of rare diseases of the Head, Neck and Teeth: results of a French population-based prospective 8-year studyLisa Friedlander, Rémy Choquet, Eva Galliani, et al.
Orphanet Journal of Rare Diseases|July 2, 2017
Prevalence of fibrodysplasia ossificans progressiva (FOP) in France: an estimate based on a record linkage of two national databasesGeneviève Baujat, Rémy Choquet, Stéphane Bouée, et al.
Annals of the Rheumatic Diseases|December 22, 2010
A multicentre, randomised, double-blind, placebo-controlled trial with the interleukin-1 receptor antagonist anakinra in patients with systemic-onset juvenile idiopathic arthritis (ANAJIS trial)Pierre Quartier, Florence Allantaz, Rolando Cimaz, et al.
Studies in Health Technology and Informatics|September 16, 2010
CEMARA an information system for rare diseasesPaul Landais, Claude Messiaen, Ana Rath, et al.
Studies in Health Technology and Informatics|May 20, 2008
CEMARA: a Web dynamic application within a N-tier architecture for rare diseasesClaude Messiaen, Loïc Le Mignot, Ana Rath, et al.
Orphanet Journal of Rare Diseases|November 5, 2021
Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseasesWafa Kallali, Claude Messiaen, Roumaisah Saïdi, et al.
Orphanet Journal of Rare Diseases|August 5, 2021
10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in FranceClaude Messiaen, Caroline Racine, Ahlem Khatim, et al.
Pageof 2