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7. [Vohwinkel's syndrome (study of 4 cases)]. Blesa Llamas G; Ocaña Sierra J; Montero E Actas Dermosifiliogr; 1974; 65(7-8):331-44. PubMed ID: 4281610 [No Abstract] [Full Text] [Related]
8. Olmsted syndrome with squamous cell carcinoma of extremities and adenocarcinoma of the lung: failure to detect loricrin gene mutation. Ogawa F; Udono M; Murota H; Shimizu K; Takahashi H; Ishida-Yamamoto A; Iizuka H; Katayama I Eur J Dermatol; 2003; 13(6):524-8. PubMed ID: 14721769 [TBL] [Abstract][Full Text] [Related]
9. [Vohwinkel's syndrome (study of 4 cases)]. Ocaña Sierra J; Blesa G; Montero E Ann Dermatol Syphiligr (Paris); 1975; 102(1):41-5. PubMed ID: 132129 [TBL] [Abstract][Full Text] [Related]
10. Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin. Camisa C; Rossana C Arch Dermatol; 1984 Oct; 120(10):1323-8. PubMed ID: 6237617 [TBL] [Abstract][Full Text] [Related]
11. An Indian case of keratoderma hereditarium mutilans (Vohwinkel's syndrome) associated with ichthyosiform dermatosis. Vijaikumar M; Thappa DM; Jeevankumar B J Dermatol; 2001 Oct; 28(10):560-3. PubMed ID: 11732725 [TBL] [Abstract][Full Text] [Related]
12. A novel insertional mutation in loricrin in Vohwinkel's Keratoderma. Armstrong DK; McKenna KE; Hughes AE J Invest Dermatol; 1998 Oct; 111(4):702-4. PubMed ID: 9764857 [TBL] [Abstract][Full Text] [Related]
13. Variant of Vohwinkel's syndrome. Ali MM; Upadya GM Indian J Dermatol Venereol Leprol; 2006; 72(6):449-51. PubMed ID: 17179623 [TBL] [Abstract][Full Text] [Related]
14. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Maestrini E; Monaco AP; McGrath JA; Ishida-Yamamoto A; Camisa C; Hovnanian A; Weeks DE; Lathrop M; Uitto J; Christiano AM Nat Genet; 1996 May; 13(1):70-7. PubMed ID: 8673107 [TBL] [Abstract][Full Text] [Related]
15. Vohwinkel's syndrome in three generations. Solis RR; Diven DG; Trizna Z J Am Acad Dermatol; 2001 Feb; 44(2 Suppl):376-8. PubMed ID: 11174420 [TBL] [Abstract][Full Text] [Related]
16. Keratoderma hereditaria mutilans or Vohwinkel's syndrome. Camisa C J Am Acad Dermatol; 1986 Mar; 14(3):512-4. PubMed ID: 2937815 [No Abstract] [Full Text] [Related]
17. Molecular quantification of human beta-glucuronidase levels in a patient with Vohwinkel's syndrome. Hughes TJ; Hughes ML; Caldwell BD J Am Podiatr Med Assoc; 2001 Mar; 91(3):114-20. PubMed ID: 11266492 [TBL] [Abstract][Full Text] [Related]
18. Loricrin gene mutation in a Japanese patient of Vohwinkel's syndrome. Takahashi H; Ishida-Yamamoto A; Kishi A; Ohara K; Iizuka H J Dermatol Sci; 1999 Jan; 19(1):44-7. PubMed ID: 9890374 [TBL] [Abstract][Full Text] [Related]