Below are the most recent publications written about "Dermatitis, Exfoliative" by people in Profiles.
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Navarro-Navarro I, Jim?nez-Gallo D, de la Varga-Mart?nez R, Villegas-Romero I, Mora-L?pez F, Linares-Barrios M, Youssefian L, Vahidnezhad H, Uitto J. Novel splice mutation in CDSN gene causing type b peeling skin syndrome. J Eur Acad Dermatol Venereol. 2022 06; 36(6):e456-e460.
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Mohamad J, Nanda A, Pavlovsky M, Peled A, Malchin N, Malovitski K, Pramanik R, Weissglas-Volkov D, Shomron N, McGrath J, Sprecher E, Sarig O. Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis. Exp Dermatol. 2020 08; 29(8):742-748.
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Onoufriadis A, Simpson JK, McDonald C, Nguyen TTM, Campeau PM, Simpson MA, Martinez AE, McGrath JA. Nonsyndromic erythrodermic ichthyosis resulting from a homozygous mutation in PIGL. Clin Exp Dermatol. 2020 Apr; 45(3):391-394.
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Duffy R, Jennings T, Kartan S, Song A, Shi W, Porcu P, Alpdogan O, Sahu J. Special Considerations in the Treatment of Mycosis Fungoides. Am J Clin Dermatol. 2019 Aug; 20(4):571-578.
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Wolf R, Parish LC, Parish JL. Commentary: The rash from nuisance to life-threatening. Clin Dermatol. 2019 Mar - Apr; 37(2):85-87.
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Mohamad J, Sarig O, Godsel LM, Peled A, Malchin N, Bochner R, Vodo D, Rabinowitz T, Pavlovsky M, Taiber S, Fried M, Eskin-Schwartz M, Assi S, Shomron N, Uitto J, Koetsier JL, Bergman R, Green KJ, Sprecher E. Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A. J Invest Dermatol. 2018 08; 138(8):1736-1743.
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Szczecinska W, Nesteruk D, Wertheim-Tysarowska K, Greenblatt DT, Baty D, Browne F, Liu L, Ozoemena L, Terron-Kwiatkowski A, McGrath JA, Mellerio JE, Morton J, Wozniak K, Kowalewski C, Has C, Moss C. Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations. Br J Dermatol. 2014 Nov; 171(5):1206-10.
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Krunic AL, Stone KL, Simpson MA, McGrath JA. Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A. Pediatr Dermatol. 2013 Sep-Oct; 30(5):e87-8.
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Pavlovic S, Krunic AL, Bulj TK, Medenica MM, Fong K, Arita K, McGrath JA. Acral peeling skin syndrome: a clinically and genetically heterogeneous disorder. Pediatr Dermatol. 2012 May-Jun; 29(3):258-63.
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van der Velden JJ, Jonkman MF, McLean WH, Hamm H, Steijlen PM, van Steensel MA, van Geel M. A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome. J Dermatol Sci. 2012 Jan; 65(1):74-6.