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European Journal of Human Genetics : EJHG|April 24, 2018
A decision tree for the genetic diagnosis of deficiency of adenosine deaminase 2 (DADA2): a French reference centres experienceMélanie Rama, Claire Duflos, Isabelle Melki, et al.Rheumatology (Oxford, England)|November 26, 2024
Prognostic factors for patients with cancer-associated dermatomyositis: a retrospective, multicentre cohort study of 73 patientsAlexandre Teboul, Yves Allenbach, Florence Tubach, et al.Frontiers in Immunology|December 16, 2020
Cytokine Signature in Schnitzler Syndrome: Proinflammatory Cytokine Production Associated to Th SuppressionMarie Masson Regnault, Eric Frouin, Isabelle Jéru, et al.Trials|June 28, 2018
Treatment of voluminous and complicated superficial slow-flow vascular malformations with sirolimus (PERFORMUS): protocol for a multicenter phase 2 trial with a randomized observational-phase designAnnabel Maruani, Olivia Boccara, Didier Bessis, et al.JAMA Dermatology|September 15, 2021
Sirolimus (Rapamycin) for Slow-Flow Malformations in Children: The Observational-Phase Randomized Clinical PERFORMUS TrialAnnabel Maruani, Elsa Tavernier, Olivia Boccara, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|November 25, 2024
Long-term effects of sirolimus treatment for slow-flow vascular malformations: Real-world evidence from the French observational multicentre SIROLO studyCécilia Maillet, Olivia Boccara, Stéphanie Mallet, et al.Trials|December 19, 2019
Topical sirolimus 0.1% for treating cutaneous microcystic lymphatic malformations in children and adults (TOPICAL): protocol for a multicenter phase 2, within-person, randomized, double-blind, vehicle-controlled clinical trialSophie Leducq, Agnès Caille, Sébastien Barbarot, et al.JAMA Dermatology|June 1, 2017
Efficacy and Tolerance of Anti-Tumor Necrosis Factor α Agents in Cutaneous Sarcoidosis: A French Study of 46 CasesValentine Heidelberger, Saskia Ingen-Housz-Oro, Alicia Marquet, et al.Journal of the American Academy of Dermatology|October 16, 2016
The scalp hair collar and tuft signs: A retrospective multicenter study of 78 patients with a systematic review of the literatureDidier Bessis, Michèle Bigorre, Nausicaa Malissen, et al.Orphanet Journal of Rare Diseases|March 24, 2016
Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencingNadège Calmels, Géraldine Greff, Cathy Obringer, et al.Pageof 14