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Smail Hadj-Rabia

Showing results (21-30 of 125) with videos related to

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Acta Dermato-Venereologica|October 6, 2012
Novel mutation in GJB4 gene (connexin 30.3) in a family with erythrokeratodermia variabilisEmilie Sbidian, Norredine Bousseloua, Laurence Jonard, et al.
Social Science & Medicine (1982)|January 30, 2025
Dyadic adjustment of persons with albinism and their significant other: A Bayesian mediation model of the Actor-Partner Interdependence (APIMeM)Hugo Fournier, Nicolas Pillaud, Fanny Morice-Picard, et al.
Clinical Genetics|October 29, 2020
Parkes-Weber syndrome related to RASA1 mosaic mutationOlivia Boccara, Mélanie Eyries, Stéphanie Pannier, et al.
American Journal of Medical Genetics. Part A|August 28, 2014
Cognitive profile of school-age children and teenagers with hypohidrotic ectodermal dysplasia (HED)Smail Hadj-Rabia, Stéphane Jacob, Hélène Dufresne, et al.
Acta Dermato-Venereologica|May 20, 2020
Novel CLDN1 Deletion Associated with Ichthyosis, Sclerosing Cholangitis and Acquired AlopeciaMaleha S Alsafri, Fabienne Charbit-Henrion, Florence Lacaille, et al.
Archives of Dermatology|July 21, 2010
Clinical spectrum of tufted angiomas in childhood: a report of 13 cases and a review of the literatureAmélie Osio, Sylvie Fraitag, Smail Hadj-Rabia, et al.
Experimental Dermatology|October 5, 2019
P63-related disorders: Dermatological characteristics in 22 patientsAlexia Maillard, Caroline Alby, Eric Gabison, et al.
Pediatric Dermatology|March 12, 2020
Hypophosphatemic rickets: A rare complication of congenital melanocytic nevus syndromeAnne Welfringer-Morin, Graziella Pinto, Geneviève Baujat, et al.
International Journal of Dermatology|January 12, 2017
Assessment of the effectiveness of topical propranolol 4% gel for infantile hemangiomasJacob Mashiah, Ana Kutz, Smail Hadj Rabia, et al.
The Journal of Allergy and Clinical Immunology|December 28, 2016
Eosinophilic esophagitis and colonic mucosal eosinophilia in Netherton syndromeColombe Paluel-Marmont, Nathalia Bellon, Patrick Barbet, et al.
Pageof 13

Showing results (21-30 of 125) with videos related to

Sort By:
Pageof 13
Acta Dermato-Venereologica|October 6, 2012
Novel mutation in GJB4 gene (connexin 30.3) in a family with erythrokeratodermia variabilisEmilie Sbidian, Norredine Bousseloua, Laurence Jonard, et al.
Social Science & Medicine (1982)|January 30, 2025
Dyadic adjustment of persons with albinism and their significant other: A Bayesian mediation model of the Actor-Partner Interdependence (APIMeM)Hugo Fournier, Nicolas Pillaud, Fanny Morice-Picard, et al.
Clinical Genetics|October 29, 2020
Parkes-Weber syndrome related to RASA1 mosaic mutationOlivia Boccara, Mélanie Eyries, Stéphanie Pannier, et al.
American Journal of Medical Genetics. Part A|August 28, 2014
Cognitive profile of school-age children and teenagers with hypohidrotic ectodermal dysplasia (HED)Smail Hadj-Rabia, Stéphane Jacob, Hélène Dufresne, et al.
Acta Dermato-Venereologica|May 20, 2020
Novel CLDN1 Deletion Associated with Ichthyosis, Sclerosing Cholangitis and Acquired AlopeciaMaleha S Alsafri, Fabienne Charbit-Henrion, Florence Lacaille, et al.
Archives of Dermatology|July 21, 2010
Clinical spectrum of tufted angiomas in childhood: a report of 13 cases and a review of the literatureAmélie Osio, Sylvie Fraitag, Smail Hadj-Rabia, et al.
Experimental Dermatology|October 5, 2019
P63-related disorders: Dermatological characteristics in 22 patientsAlexia Maillard, Caroline Alby, Eric Gabison, et al.
Pediatric Dermatology|March 12, 2020
Hypophosphatemic rickets: A rare complication of congenital melanocytic nevus syndromeAnne Welfringer-Morin, Graziella Pinto, Geneviève Baujat, et al.
International Journal of Dermatology|January 12, 2017
Assessment of the effectiveness of topical propranolol 4% gel for infantile hemangiomasJacob Mashiah, Ana Kutz, Smail Hadj Rabia, et al.
The Journal of Allergy and Clinical Immunology|December 28, 2016
Eosinophilic esophagitis and colonic mucosal eosinophilia in Netherton syndromeColombe Paluel-Marmont, Nathalia Bellon, Patrick Barbet, et al.
Pageof 13