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Neutrophilic dermatoses.
Delaleu, J; Lepelletier, C; Calugareanu, A; De Masson, A; Charvet, E; Petit, A; Giurgea, I; Amselem, S; Karabina, S; Jachiet, M; Mahevas, T; Ram-Wolff, C; Vignon-Pennamen, M-D; Bagot, M; Battistella, M; Bouaziz, J-D.
Affiliation
  • Delaleu J; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France; Inserm u933, "Childhood genetic disorders", service de génétique, Sorbonne université, hôpital Armand-Trousseau, AP-HP, Paris,
  • Lepelletier C; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France.
  • Calugareanu A; Service de dermatologie, Severe Cutaneous Adverse Reaction (SCAR) Regional Center, HCL, CHU de Lyon Centre, Lyon, France.
  • De Masson A; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France.
  • Charvet E; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France.
  • Petit A; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France.
  • Giurgea I; Inserm u933, "Childhood genetic disorders", service de génétique, Sorbonne université, hôpital Armand-Trousseau, AP-HP, Paris, France.
  • Amselem S; Inserm u933, "Childhood genetic disorders", service de génétique, Sorbonne université, hôpital Armand-Trousseau, AP-HP, Paris, France.
  • Karabina S; Inserm u933, "Childhood genetic disorders", service de génétique, Sorbonne université, hôpital Armand-Trousseau, AP-HP, Paris, France.
  • Jachiet M; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France.
  • Mahevas T; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France.
  • Ram-Wolff C; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France.
  • Vignon-Pennamen MD; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France; Service d'anatomie pathologique, hôpital Saint-Louis, AP-HP, Paris, France.
  • Bagot M; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France.
  • Battistella M; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France; Service d'anatomie pathologique, hôpital Saint-Louis, AP-HP, Paris, France.
  • Bouaziz JD; Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France. Electronic address: jean-david.bouaziz@aphp.fr.
Rev Med Interne ; 43(12): 727-738, 2022 Dec.
Article in En | MEDLINE | ID: mdl-35870984
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases, Vesiculobullous / Sweet Syndrome / Pyoderma Gangrenosum / Vasculitis, Leukocytoclastic, Cutaneous Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Rev Med Interne Year: 2022 Document type: Article Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases, Vesiculobullous / Sweet Syndrome / Pyoderma Gangrenosum / Vasculitis, Leukocytoclastic, Cutaneous Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Rev Med Interne Year: 2022 Document type: Article Country of publication: