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The British Journal of Dermatology|July 1, 1994
Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 casesC Bodemer, Y De Prost, B Bachollet, et al.European Journal of Human Genetics : EJHG|June 15, 2000
Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysisP Lefevre, A Rochat, C Bodemer, et al.Human Molecular Genetics|November 2, 2001
Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with agingY Gache, M Allegra, C Bodemer, 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.Annales De Dermatologie Et De Venereologie|December 22, 1999
[Scleroderma in children: a retrospective study of 70 cases]C Bodemer, M Belon, D Hamel-Teillac, et al.Annales De Pediatrie|September 1, 1992
[Kasabach-Merritt syndrome in children]D Teillac-Hamel, P Andry, C Bodemer, et al.Acta Dermato-Venereologica. Supplementum|January 1, 1992
Management of severe atopic dermatitisY de ProstAnnales De Dermatologie Et De Venereologie|June 30, 2005
[The value of topical immunosuppressors in the treatment of atopic dermatitis in children]Y de ProstJournal 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.Pageof 38