Lupus erythematosus and epidermal necrolysis: a case series of 16 patients.

Gaudin, O; Milpied, B; Papouin, B; Hüe, S; Ortonne, N; Régnier, E; Wolkenstein, P; Chosidow, O; de Prost, N; Ingen-Housz-Oro, S

Gaudin, O; Milpied, B; Papouin, B; Hüe, S; Ortonne, N; Régnier, E; Wolkenstein, P; Chosidow, O; de Prost, N; Ingen-Housz-Oro, S.

Afiliação

Gaudin O; Dermatology Department, AP-HP, Henri Mondor Hospital, Créteil, France.
Milpied B; Reference Center for Toxic Bullous Diseases and Severe Drug Reactions TOXIBUL, Créteil, France.
Papouin B; Reference Center for Toxic Bullous Diseases and Severe Drug Reactions TOXIBUL, Créteil, France.
Hüe S; Dermatology Department, Saint André Hospital, Bordeaux, France.
Ortonne N; Pathology Department, AP-HP, Henri Mondor Hospital, Créteil, France.
Régnier E; Université Paris-Est Créteil Val de Marne, UPEC, Créteil, France.
Wolkenstein P; INSERM U955, Université Paris Est Créteil Val de Marne, UPEC, Créteil, France.
Chosidow O; Immunology Department, AP-HP, Henri Mondor Hospital, Créteil, France.
de Prost N; Pathology Department, AP-HP, Henri Mondor Hospital, Créteil, France.
Ingen-Housz-Oro S; Université Paris-Est Créteil Val de Marne, UPEC, Créteil, France.

Br J Dermatol ; 186(2): 372-374, 2022 02.

Article em En | MEDLINE | ID: mdl-34597413

Assuntos

Lúpus Eritematoso Sistêmico; Síndrome de Stevens-Johnson; Humanos; Síndrome de Stevens-Johnson/complicações; Síndrome de Stevens-Johnson/diagnóstico

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Stevens-Johnson / Lúpus Eritematoso Sistêmico Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Br J Dermatol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

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