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Smail Hadj-Rabia

Showing results (41-50 of 125) with videos related to

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European Journal of Dermatology : EJD|August 28, 2024
Hydroelectrolytic and nutritional needs of infants with epidermolysis bullosa during the first month of lifeHélène Schieber, Smail Hadj-Rabia, Agnès Giuseppi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 11, 2026
Founder effect and clinical heterogeneity of SLC27A4-related non-syndromic EDD in RéunionJuliette Miquel, Constance Deblock, Sarah Ventejou, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 28, 2026
Genetic sequencing strategy for the diagnosis of epidermal differentiation disorders: A cohort studyConstance Deblock, Adrienne Elmorjani, Nathalia Bellon, et al.
The British Journal of Dermatology|September 1, 2025
The Tryptophan-Serotonin Axis in Albinism: an interesting lead?Benoît Gendrot, Marion Falabregue, Camille Huet, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 29, 2024
Drugs associated with epidermal necrolysis in children: A World Health Organization pharmacovigilance database analysisPauline Bataille, Benedicte Lebrun-Vignes, Thomas Bettuzzi, et al.
The British Journal of Dermatology|February 10, 2023
Severe tracheal involvement in type XVII collagen junctional epidermolysis bullosaAlizée Bozonnat, Laura Polivka, Stéphanie Leclerc-Mercier, et al.
The Journal of Investigative Dermatology|March 26, 2017
Do the Side Effects of BRAF Inhibitors Mimic RASopathies?Alicia Sfecci, Alain Dupuy, Monica Dinulescu, et al.
Acta Dermato-Venereologica|November 29, 2013
Cutaneous location of atypical teratoid/rhabdoid tumourNathalia Bellon, Sylvie Fraitag, Catherine Miquel, et al.
Pediatric Dermatology|March 19, 2022
Evaluation of neurodevelopmental symptoms in 10 cases of neonatal ichthyosis and sclerosing cholangitis syndromeDeborah Salik, Smail Hadj-Rabia, Daniel Hohl, et al.
Acta Dermato-Venereologica|April 19, 2017
Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile MyofibromatosisClemence Lepelletier, Yasser Al-Sarraj, Christine Bodemer, et al.
Pageof 13

Showing results (41-50 of 125) with videos related to

Sort By:
Pageof 13
European Journal of Dermatology : EJD|August 28, 2024
Hydroelectrolytic and nutritional needs of infants with epidermolysis bullosa during the first month of lifeHélène Schieber, Smail Hadj-Rabia, Agnès Giuseppi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 11, 2026
Founder effect and clinical heterogeneity of SLC27A4-related non-syndromic EDD in RéunionJuliette Miquel, Constance Deblock, Sarah Ventejou, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 28, 2026
Genetic sequencing strategy for the diagnosis of epidermal differentiation disorders: A cohort studyConstance Deblock, Adrienne Elmorjani, Nathalia Bellon, et al.
The British Journal of Dermatology|September 1, 2025
The Tryptophan-Serotonin Axis in Albinism: an interesting lead?Benoît Gendrot, Marion Falabregue, Camille Huet, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 29, 2024
Drugs associated with epidermal necrolysis in children: A World Health Organization pharmacovigilance database analysisPauline Bataille, Benedicte Lebrun-Vignes, Thomas Bettuzzi, et al.
The British Journal of Dermatology|February 10, 2023
Severe tracheal involvement in type XVII collagen junctional epidermolysis bullosaAlizée Bozonnat, Laura Polivka, Stéphanie Leclerc-Mercier, et al.
The Journal of Investigative Dermatology|March 26, 2017
Do the Side Effects of BRAF Inhibitors Mimic RASopathies?Alicia Sfecci, Alain Dupuy, Monica Dinulescu, et al.
Acta Dermato-Venereologica|November 29, 2013
Cutaneous location of atypical teratoid/rhabdoid tumourNathalia Bellon, Sylvie Fraitag, Catherine Miquel, et al.
Pediatric Dermatology|March 19, 2022
Evaluation of neurodevelopmental symptoms in 10 cases of neonatal ichthyosis and sclerosing cholangitis syndromeDeborah Salik, Smail Hadj-Rabia, Daniel Hohl, et al.
Acta Dermato-Venereologica|April 19, 2017
Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile MyofibromatosisClemence Lepelletier, Yasser Al-Sarraj, Christine Bodemer, et al.
Pageof 13