Primary skin lymphomas: Current therapy von Dereure, O

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Cutis marmorata telangiectatica congenita: Mutations in a susceptibility gene involved in cerebrovascular accidents von Dereure, O

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"Typical" epidermodysplasia verruciformis: Identification of a molecular complex regulating keratinocyte innate immunity von Dereure, O

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Hereditary fibrosing poikiloderma with contractures, myopathy and pulmonary fibrosis: The role of mutations in FAM111B von Dereure, O

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Blastic plasmacytoid dendritic cell neoplasm: clinical features in 90 patients von Julia, F., Petrella, T., Beylot-Barry, M., Bagot, M., Lipsker, D., Machet, L., Joly, P., Dereure, O., Wetterwald, M., d'Incan, M., Grange, F., Cornillon, J., Tertian, G., Maubec, E., Saiag, P., Barete, S., Templier, I., Aubin, F., Dalle, S.

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Permanent scalp alopecia related to breast cancer chemotherapy by sequential fluorouracil/epirubicin/cyclophosphamide (FEC) and docetaxel: a prospective study of 20 patients von Kluger, N., Jacot, W., Frouin, E., Rigau, V., Poujol, S., Dereure, O., Guillot, B., Romieu, G., Bessis, D.

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Progressive symmetric erythrokeratodermia: Activating mutations of TRPM4 von Dereure, O

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Epstein-Barr Virus-related Multi-site Mucocutaneous Ulcer: A Previously Undescribed Clinical Subset of a Rare Disease von Schwob, Emilie, Szablewski, Vanessa, Lerisson, Mathilde, Dereure, Olivier

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Involvement of cholesterol metabolism in hypotrichosis simplex von Dereure, O

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Effectiveness of mogamulizumab in patients with Mycosis Fungoides or Sézary syndrome: A multicentre, retrospective, real‐world French study von Beylot‐Barry, M., Quereux, G., Nardin, C., Duval‐Modeste, A.‐B., Dereure, O., Dalac‐Rat, S., Dobos, G., Pham‐Ledard, A., Ram‐Wolff, C., D'Incan, M., Grange, F., Braniste, V., Bagot, M.

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Huriez syndrome finally explained: Haploinsufficiency of a gene involved in homologous recombination DNA repair von Dereure, O

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Symmetrical acral keratoderma: The role of transcription-factor mutations von Dereure, O

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Immune checkpoint blockade in oncodermatology: An ongoing revolution von Dereure, O

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Autosomal recessive cutis laxa: New genes identified von Dereure, O

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Autosomal-recessive amylosis cutis dyschromica and GPNMB mutations von Dereure, O

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Congenital ichtyosis to have its own biotherapies? von Dereure, O

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Drug-induced skin pigmentation. Epidemiology, diagnosis and treatment von Dereure, O

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Management of ocular involvement in the acute phase of Stevens-Johnson syndrome and toxic epidermal necrolysis: french national audit of practices, literature review, and consensus... von Thorel, D, Ingen-Housz-Oro, S, Royer, G, Delcampe, A, Bellon, N, Bodemer, C, Welfringer-Morin, A, Bremond-Gignac, D, Robert, M P, Tauber, M, Malecaze, F, Dereure, O, Daien, V, Colin, A, Bernier, C, Couret, C, Vabres, B, Tetart, F, Milpied, B, Cornut, T, Ben Said, B, Burillon, C, Cordel, N, Beral, L, de Prost, N, Wolkenstein, P, Muraine, M, Gueudry, J

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Characterization of patients with advanced basal cell carcinoma progressing while receiving Hedgehog pathway inhibitors von Monnet, P., Herms, F., Djermane, M., Dalac, S., Dereure, O., Dréno, B., Beylot‐Barry, M., Mortier, L., Basset‐Seguin, N.

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Isolated nonsyndromic nail dysplasia: Homozygous mutation in SLC25A16 von Dereure, O

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