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23. KRT9 gene mutation as a reliable indicator in the prenatal molecular diagnosis of epidermolytic palmoplantar keratoderma. Ke HP; Jiang HL; Lv YS; Huang YZ; Liu RR; Chen XL; Du ZF; Luo YQ; Xu CM; Fan QH; Zhang XN Gene; 2014 Aug; 546(1):124-8. PubMed ID: 24862219 [TBL] [Abstract][Full Text] [Related]
24. Treatment of pachyonychia congenita with plantar injections of botulinum toxin. Swartling C; Vahlquist A Br J Dermatol; 2006 Apr; 154(4):763-5. PubMed ID: 16536826 [TBL] [Abstract][Full Text] [Related]
25. Six generations of epidermolytic palmoplantar keratoderma, associated with a KRT9 R163W mutation. Wang P; Kang XJ; Tang XH; Liu JY; Li WZ; Wang WJ; Liang SN; Feng YY; Ding Y; Chen WJ Cancer Genet; 2016 Nov; 209(11):515-524. PubMed ID: 27864007 [TBL] [Abstract][Full Text] [Related]
26. Possible anticipation in familial epidermolytic palmoplantar keratoderma with the p.R163W mutation of Keratin 9. Guo Y; Shi M; Tan ZP; Shi XL Genet Mol Res; 2014 Oct; 13(4):8089-93. PubMed ID: 25299193 [TBL] [Abstract][Full Text] [Related]
27. Hereditary callosities with blisters. Report of a family and review. Baden HP; Bronstein BR; Rand RE J Am Acad Dermatol; 1984 Sep; 11(3):409-15. PubMed ID: 6237131 [TBL] [Abstract][Full Text] [Related]
28. First case of pachyonychia congenita in the Czech Republic. Jiráková A; Rajská L; Rob F; Džambová M; Sečníková Z; Göpfertová D; Schwartz M; Smith F; Lotti T; Hercogová J Dermatol Ther; 2015; 28(1):10-2. PubMed ID: 25174302 [TBL] [Abstract][Full Text] [Related]
29. A novel mutation within the 2B rod domain of keratin 9 in a Chinese pedigree with epidermolytic palmoplantar keratoderma combined with knuckle pads and camptodactyly. Du ZF; Wei W; Wang YF; Chen XL; Chen CY; Liu WT; Lu JJ; Mao LG; Xu CM; Fang H; Zhang XN Eur J Dermatol; 2011; 21(5):675-9. PubMed ID: 21715251 [TBL] [Abstract][Full Text] [Related]
30. [Familial palmo-plantar keratoderma with epidermolytic hyperkeratosis (author's transl)]. Moulin G; Bouchet R Ann Dermatol Venereol; 1977 Jan; 104(1):38-44. PubMed ID: 14586 [TBL] [Abstract][Full Text] [Related]
31. Mal de Meleda: a new geographical localization in Anatolia. Ergin S; Erdogan BS; Aktan S Dermatology; 2003; 206(2):124-30. PubMed ID: 12592079 [TBL] [Abstract][Full Text] [Related]
32. Epidermolytic palmo-plantar keratoderma. Thomas JR; Greene SL; Su WP Int J Dermatol; 1984 Dec; 23(10):652-5. PubMed ID: 6241180 [TBL] [Abstract][Full Text] [Related]
33. Keratin 17 Mutations in Four Families from India with Pachyonychia Congenita. Agarwala M; Salphale P; Peter D; Wilson NJ; Pulimood S; Schwartz ME; Smith FJD Indian J Dermatol; 2017; 62(4):422-426. PubMed ID: 28794556 [TBL] [Abstract][Full Text] [Related]
34. De novo mutation of keratin 9 gene in two Taiwanese patients with epidermolytic palmoplantar keratoderma. Yang MH; Lee JY; Lin JH; Chao SC J Formos Med Assoc; 2003 Jul; 102(7):492-6. PubMed ID: 14517588 [TBL] [Abstract][Full Text] [Related]
35. Malignant melanoma developing in an area of hereditary palmoplantar keratoderma (Mal de Meleda). Mozzillo N; Nunziata CA; Caracò C; Fazioli F; Botti G; J Surg Oncol; 2003 Dec; 84(4):229-33. PubMed ID: 14756434 [TBL] [Abstract][Full Text] [Related]
36. Hereditary palmoplantar keratoderma and dermatophytosis in the northernmost county of Sweden (Norrbotten). Nielsen PG Acta Derm Venereol Suppl (Stockh); 1994; 188():1-60. PubMed ID: 9868488 [TBL] [Abstract][Full Text] [Related]
37. Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland. Covello SP; Irvine AD; McKenna KE; Munro CS; Nevin NC; Smith FJ; Uitto J; McLean WH J Invest Dermatol; 1998 Dec; 111(6):1207-9. PubMed ID: 9856842 [TBL] [Abstract][Full Text] [Related]
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40. Mutations in a keratin 6 isomer (K6c) cause a type of focal palmoplantar keratoderma. Bowden PE J Invest Dermatol; 2010 Feb; 130(2):336-8. PubMed ID: 20081885 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]