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Annales De Dermatologie Et De Venereologie|December 25, 2018
[Nagashima-type palmoplantar keratoderma: A little-known palmoplantar keratoderma in Europe]K Chassain, A Croué, E Blanchard, et al.Orphanet Journal of Rare Diseases|June 12, 2021
Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive careM Marro, S De Smet, D Caldari, et al.Journal of Cutaneous Pathology|July 21, 2009
Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermasS Leclerc-Mercier, C Bodemer, E Bourdon-Lanoy, et al.Annales De Dermatologie Et De Venereologie|June 23, 2012
[Clinical features of Spitz naevus in children: a retrospective study of 196 cases]L Le Saché-de Peufeilhoux, I Moulonguet, B Cavelier-Balloy, et al.The British Journal of Dermatology|September 10, 2020
Genotypic and Phenotypic Analysis of 34 Cases of Inherited Junctional Epidermolysis Bullosa caused by COL17A1 MutationsA Charlesworth, A L Hérissé, N Bellon, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|February 1, 2019
Long-term evolving profile of childhood autoimmune blistering diseases: Retrospective study on 38 childrenA Welfringer-Morin, L Bekel, N Bellon, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|March 15, 2019
Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literatureS Leclerc-Mercier, D Moshous, B Neven, et al.Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|January 31, 2014
Live rubella virus vaccine long-term persistence as an antigenic trigger of cutaneous granulomas in patients with primary immunodeficiencyC Bodemer, V Sauvage, N Mahlaoui, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|May 27, 2021
Management of albinism: French guidelines for diagnosis and careE Moreno-Artero, F Morice-Picard, D Bremond-Gignac, et al.The British Journal of Dermatology|June 2, 2020
The challenging management of a series of 43 infants with Netherton syndrome: unexpected complications and novel mutationsN Bellon, S Hadj-Rabia, F Moulin, et al.Pageof 2