725 related articles for article (PubMed ID: 16403113)
1. Towards characterization of palmoplantar keratoderma caused by gain-of-function mutation in loricrin: analysis of a family and review of the literature.
Gedicke MM; Traupe H; Fischer B; Tinschert S; Hennies HC
Br J Dermatol; 2006 Jan; 154(1):167-71. PubMed ID: 16403113
[TBL] [Abstract][Full Text] [Related]
2. Collodion baby and loricrin keratoderma: a case report and mutation analysis.
Yeh JM; Yang MH; Chao SC
Clin Exp Dermatol; 2013 Mar; 38(2):147-50. PubMed ID: 22831754
[TBL] [Abstract][Full Text] [Related]
3. A novel c.545-546insG mutation in the loricrin gene correlates with a heterogeneous phenotype of loricrin keratoderma.
Song S; Shen C; Song G; Mao X; Yan G; Wang X; Yan M; Zhong N
Br J Dermatol; 2008 Sep; 159(3):714-9. PubMed ID: 18844868
[TBL] [Abstract][Full Text] [Related]
4. Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby.
Matsumoto K; Muto M; Seki S; Saida T; Horiuchi N; Takahashi H; Ishida-Yamamoto A; Iizuka H
Br J Dermatol; 2001 Oct; 145(4):657-60. PubMed ID: 11703298
[TBL] [Abstract][Full Text] [Related]
5. Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia.
Wei S; Zhou Y; Zhang TD; Huang ZM; Zhang XB; Zhu HL; Liang BH; Lin L; Deng L
Clin Exp Dermatol; 2011 Jun; 36(4):399-405. PubMed ID: 21198793
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness.
Sevior KB; Hatamochi A; Stewart IA; Bykhovskaya Y; Allen-Powell DR; Fischel-Ghodsian N; Maw MA
Am J Med Genet; 1998 Jan; 75(2):179-85. PubMed ID: 9450881
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. Identification of two new mutations in the TAT gene in a Danish family with tyrosinaemia type II.
Pasternack SM; Betz RC; Brandrup F; Gade EF; Clemmensen O; Lund AM; Christensen E; Bygum A
Br J Dermatol; 2009 Mar; 160(3):704-6. PubMed ID: 18945316
[No Abstract] [Full Text] [Related]
10. De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma.
Drera B; Tadini G; Balbo F; Marchese L; Barlati S; Colombi M
Clin Genet; 2008 Jan; 73(1):85-8. PubMed ID: 17953701
[No Abstract] [Full Text] [Related]
11. Dermoscopic furrow ink test of the palmar lesion in loricrin keratoderma.
Shirahama T; Hamada T; Abe T; Arakawa M; Teye K; Koga H; Ishii N; Nakama T
J Dermatol; 2022 Aug; 49(8):783-786. PubMed ID: 35467044
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis).
Schmuth M; Fluhr JW; Crumrine DC; Uchida Y; Hachem JP; Behne M; Moskowitz DG; Christiano AM; Feingold KR; Elias PM
J Invest Dermatol; 2004 Apr; 122(4):909-22. PubMed ID: 15102081
[TBL] [Abstract][Full Text] [Related]
14. Abnormal cornified cell envelope formation in mutilating palmoplantar keratoderma unrelated to epidermal differentiation complex.
Akiyama M; Christiano AM; Yoneda K; Shimizu H
J Invest Dermatol; 1998 Jul; 111(1):133-8. PubMed ID: 9665400
[TBL] [Abstract][Full Text] [Related]
15. A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma.
Kinsler VA; Drury S; Khan A; Waelchli R; Rukaite G; Barnicoat A; Lench N; Harper JI; O'Shaughnessy RF
Br J Dermatol; 2015 Jan; 172(1):262-4. PubMed ID: 25142840
[No Abstract] [Full Text] [Related]
16. Mild collodion baby as a presenting sign of loricrin keratoderma: report of a case and review of the literature.
Muñoz-Aceituno E; Nogera-Morel L; Torrelo A; Hernandez-Martin A
Clin Exp Dermatol; 2020 Apr; 45(3):395-398. PubMed ID: 31595526
[No Abstract] [Full Text] [Related]
17. Diffuse nonepidermolytic palmoplantar keratoderma caused by a recurrent nonsense mutation in DSG1.
Keren H; Bergman R; Mizrachi M; Kashi Y; Sprecher E
Arch Dermatol; 2005 May; 141(5):625-8. PubMed ID: 15897387
[TBL] [Abstract][Full Text] [Related]
18. Loricrin keratoderma: a novel disease entity characterized by nuclear accumulation of mutant loricrin.
Ishida-Yamamoto A
J Dermatol Sci; 2003 Feb; 31(1):3-8. PubMed ID: 12615358
[TBL] [Abstract][Full Text] [Related]
19. Congenital ichthyosiform dermatosis with linear keratotic flexural papules and sclerosing palmoplantar keratoderma.
Pujol RM; Moreno A; Alomar A; de Moragas JM
Arch Dermatol; 1989 Jan; 125(1):103-6. PubMed ID: 2521286
[TBL] [Abstract][Full Text] [Related]
20. A novel keratin 9 gene mutation (Asn160His) in a Taiwanese family with epidermolytic palmoplantar keratoderma.
Lin JH; Lin MH; Yang MH; Chao SC
Clin Exp Dermatol; 2004 May; 29(3):308-10. PubMed ID: 15115518
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
