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Journal Abstract Search
135 related items for PubMed ID: 32052849
21. Identification of a de novo keratin 1 mutation in epidermolytic hyperkeratosis with palmoplantar involvement. Math A, Frank J, Handisurya A, Poblete-Gutiérrez P, Slupetzky K, Födinger D, Winter D, Stingl G, Kirnbauer R. Eur J Dermatol; 2006; 16(5):507-10. PubMed ID: 17101470 [Abstract] [Full Text] [Related]
22. Mutations of keratin 9 in two families with palmoplantar epidermolytic hyperkeratosis. Bonifas JM, Matsumura K, Chen MA, Berth-Jones J, Hutchison PE, Zloczower M, Fritsch PO, Epstein EH. J Invest Dermatol; 1994 Oct; 103(4):474-7. PubMed ID: 7523529 [Abstract] [Full Text] [Related]
23. A novel nonepidermolytic palmoplantar keratoderma: a clinical and histopathologic study of six cases. Magro CM, Baden LA, Crowson AN, Bowden PE, Baden HP. J Am Acad Dermatol; 1997 Jul; 37(1):27-33. PubMed ID: 9216520 [Abstract] [Full Text] [Related]
24. Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratoderma. Yang JM, Lee S, Kang HJ, Lee JH, Yeo UC, Son IY, Park KB, Steinert PM, Lee ES. Acta Derm Venereol; 1998 Nov; 78(6):412-6. PubMed ID: 9833037 [Abstract] [Full Text] [Related]
25. Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene. Terron-Kwiatkowski A, Terrinoni A, Didona B, Melino G, Atherton DJ, Irvine AD, McLean WH. Br J Dermatol; 2004 Jun; 150(6):1096-103. PubMed ID: 15214894 [Abstract] [Full Text] [Related]
26. A unique pattern of dyskeratosis characterizes epidermolytic hyperkeratosis and epidermolytic palmoplantar keratoderma. Bergman R, Khamaysi Z, Sprecher E. Am J Dermatopathol; 2008 Apr; 30(2):101-5. PubMed ID: 18360110 [Abstract] [Full Text] [Related]
27. Diagnosis and Management of Inherited Palmoplantar Keratodermas. Thomas BR, O'Toole EA. Acta Derm Venereol; 2020 Mar 25; 100(7):adv00094. PubMed ID: 32147745 [Abstract] [Full Text] [Related]
29. Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutation. Küster W, Reis A, Hennies HC. Arch Dermatol Res; 2002 Aug 09; 294(6):268-72. PubMed ID: 12192490 [Abstract] [Full Text] [Related]
30. A de novo mutation of KRT1 in a baby girl causing epidermolytic ichthyosis with impressive epidermolytic palmoplantar keratoderma. Calì F, Failla P, Vinci M, Siragusa M, Schepis C. Dermatol Online J; 2020 Jul 15; 26(7):. PubMed ID: 32898404 [Abstract] [Full Text] [Related]
31. Mutation S233L in the 1B domain of keratin 1 causes epidermolytic palmoplantar keratoderma with "tonotubular" keratin. Terron-Kwiatkowski A, van Steensel MA, van Geel M, Lane EB, McLean WH, Steijlen PM. J Invest Dermatol; 2006 Mar 15; 126(3):607-13. PubMed ID: 16439967 [Abstract] [Full Text] [Related]
32. Identification of the keratin K9 R162W mutation in patients of Italian origin with epidermolytic palmoplantar keratoderma. Terrinoni A, Cocuroccia B, Gubinelli E, Zambruno G, Candi E, Melino G, Girolomoni G. Eur J Dermatol; 2004 Mar 15; 14(6):375-8. PubMed ID: 15564199 [Abstract] [Full Text] [Related]
38. Novel mutations in DSG1 causing striate palmoplantar keratoderma. Hershkovitz D, Lugassy J, Indelman M, Bergman R, Sprecher E. Clin Exp Dermatol; 2009 Mar 15; 34(2):224-8. PubMed ID: 19018793 [Abstract] [Full Text] [Related]
39. Two different clinical and genetic forms of hereditary palmoplantar keratoderma in the northernmost county of Sweden. Gamborg Nielsen P. Clin Genet; 1985 Nov 15; 28(5):361-6. PubMed ID: 2935332 [Abstract] [Full Text] [Related]
40. Novel and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubules. Grimberg G, Hausser I, Müller FB, Wodecki K, Schaffrath C, Krieg T, Oji V, Traupe H, Arin MJ. Br J Dermatol; 2009 Feb 15; 160(2):446-9. PubMed ID: 18795921 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]