Below are the most recent publications written about "Dermatitis" by people in Profiles.
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Hoenig LJ, Brenner S, Wolf R, Ingber A, Grant-Kels JM, Lipsker D, Parish LC. Eponyms and clinical entities from the land of Israel. Clin Dermatol. 2024 Mar-Apr; 42(2):201-205.
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Mank VMF, Arter Z, Mignano S, Burke K, Cho S. Neutrophilic Dermatosis of the Dorsal Hand: A Distinctive Variant of Sweet Syndrome. Cutis. 2023 11; 112(5):E40-E41.
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De Antonis C, Hyde JT, Lee JB, Hsu S. An unusual presentation of pigmented purpuric lichenoid dermatitis. Dermatol Online J. 2023 Oct 15; 29(5).
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Gaspari AA, Turrentine J. Dermatitis 2023: Where Are We Today? Dermatitis. 2023 Nov-Dec; 34(6):478-479.
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Inan S, Ward SJ, Baltazar CT, Peruggia GA, Javed E, Nayak AP. Epicutaneous Sensitization to the Phytocannabinoid ?-Caryophyllene Induces Pruritic Inflammation. Int J Mol Sci. 2023 Sep 20; 24(18).
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Aevermann BD, Di Domizio J, Olah P, Saidoune F, Armstrong JM, Bachelez H, Barker J, Haniffa M, Julia V, Juul K, Krishnaswamy JK, Litman T, Parsons I, Sarin KY, Schmuth M, Sierra M, Simpson M, Homey B, Griffiths CEM, Scheuermann RH, Gilliet M. Cross-Comparison of Inflammatory Skin Disease Transcriptomics Identifies PTEN as a Pathogenic Disease Classifier in Cutaneous Lupus Erythematosus. J Invest Dermatol. 2024 02; 144(2):252-262.e4.
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Vahidnezhad H, Youssefian L, Saeidian AH, Ziaee V, Mahmoudi H, Parvaneh N, Ashjaei B, Shahrokh S, Kamyab Hesari K, Soltani Zangbar M, Yousefi M, Zeinali S, Uitto J. Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance. JAMA Dermatol. 2021 Dec 01; 157(12):1466-1471.
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Aira LE, Debes GF. Skin-Homing Regulatory B Cells Required for Suppression of Cutaneous Inflammation. J Invest Dermatol. 2021 08; 141(8):1995-2005.e6.
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Cruz PCD, Gaspari AA. Dermatitis: Past, Present, Future. Dermatitis. 2021 Jan-Feb 01; 32(1):3-4.
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Kalay Yildizhan I, G?kpinar Ili E, Onoufriadis A, Kocyigit P, Kesidou E, Simpson MA, McGrath JA, Kutlay NY, Kundakci N. New Homozygous Missense MSMO1 Mutation in Two Siblings with SC4MOL Deficiency Presenting with Psoriasiform Dermatitis. Cytogenet Genome Res. 2020; 160(9):523-530.