321 related articles for article (PubMed ID: 20518786)
1. Mapping of a novel locus for an autosomal recessive form of palmoplantar keratoderma on chromosome 3q27.2-q29.
Khan S; Muzaffar S; Tariq M; Khan A; Basit S; Ahmad W
Br J Dermatol; 2010 Oct; 163(4):711-8. PubMed ID: 20518786
[TBL] [Abstract][Full Text] [Related]
2. Refined localization of a punctate palmoplantar keratoderma gene to a 5.06-cM region at 15q22.2-15q22.31.
Gao M; Yang S; Li M; Yan KL; Jiang YX; Cui Y; Xiao FL; Shen YJ; Chen JJ; Liu JB; Xu SJ; Huang W; Zhang XJ
Br J Dermatol; 2005 May; 152(5):874-8. PubMed ID: 15888140
[TBL] [Abstract][Full Text] [Related]
3. Palmoplantar keratoderma in association with carcinoma of the esophagus maps to chromosome 17q distal to the keratin gene cluster.
Hennies HC; Hagedorn M; Reis A
Genomics; 1995 Sep; 29(2):537-40. PubMed ID: 8666405
[TBL] [Abstract][Full Text] [Related]
4. Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas.
Stevens HP; Kelsell DP; Bryant SP; Bishop DT; Spurr NK; Weissenbach J; Marger D; Marger RS; Leigh IM
Arch Dermatol; 1996 Jun; 132(6):640-51. PubMed ID: 8651714
[TBL] [Abstract][Full Text] [Related]
5. [Mal de Meleda. 16 cases].
Marrakchi Z; Marrachi S; Meziou TJ; Turki H; Zahaf A
Tunis Med; 2006 Jul; 84(7):423-6. PubMed ID: 17039733
[TBL] [Abstract][Full Text] [Related]
6. Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster.
Hennies HC; Küster W; Mischke D; Reis A
Hum Mol Genet; 1995 Jun; 4(6):1015-20. PubMed ID: 7544663
[TBL] [Abstract][Full Text] [Related]
7. Hereditary epidermolytic palmoplantar keratoderma.
Blasik LG; Dimond RL; Baughman RD
Arch Dermatol; 1981 Apr; 117(4):229-31. PubMed ID: 6452099
[TBL] [Abstract][Full Text] [Related]
8. Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation.
Akasaka E; Nakano H; Nakano A; Toyomaki Y; Takiyoshi N; Rokunohe D; Nishikawa Y; Korekawa A; Matsuzaki Y; Mitsuhashi Y; Sawamura D
Br J Dermatol; 2011 Dec; 165(6):1290-2. PubMed ID: 21801157
[TBL] [Abstract][Full Text] [Related]
9. Hereditary palmoplantar keratoderma associated with primary (congenital) lymphedema.
Ogunbiyi SO; Deguara J; Moss C; Burnand KG
Lymphology; 2009 Jun; 42(2):85-7. PubMed ID: 19725273
[TBL] [Abstract][Full Text] [Related]
10. Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).
Reis A; Hennies HC; Langbein L; Digweed M; Mischke D; Drechsler M; Schröck E; Royer-Pokora B; Franke WW; Sperling K
Nat Genet; 1994 Feb; 6(2):174-9. PubMed ID: 7512862
[TBL] [Abstract][Full Text] [Related]
11. Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24.
Martinez-Mir A; Zlotogorski A; Londono D; Gordon D; Grunn A; Uribe E; Horev L; Ruiz IM; Davalos NO; Alayan O; Liu J; Gilliam TC; Salas-Alanis JC; Christiano AM
J Med Genet; 2003 Dec; 40(12):872-8. PubMed ID: 14684683
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani families.
Akbar A; Prince C; Payne C; Fasham J; Ahmad W; Baple EL; Crosby AH; Harlalka GV; Gul A
BMC Med Genet; 2019 Aug; 20(1):145. PubMed ID: 31443639
[TBL] [Abstract][Full Text] [Related]
15. [Mapping the gene for palmoplantar hyperkeratosis (thylosis) to chromosome 17 in the 17q12-q24 region].
Rogaev EI; Rogaeva EA; Ginter EK; Korovaĭtseva GI; Farrer L; Shlenskiĭ AB; Prytkov AN; St George-Hyslop P; Mordovtsev VN
Genetika; 1994 Mar; 30(3):326-9. PubMed ID: 7514555
[TBL] [Abstract][Full Text] [Related]
16. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.
Naeem M; Muhammad D; Ahmad W
Br J Dermatol; 2005 Jul; 153(1):46-50. PubMed ID: 16029325
[TBL] [Abstract][Full Text] [Related]
17. Identification of a locus for punctate palmoplantar keratodermas at chromosome 8q24.13-8q24.21.
Zhang XJ; Li M; Gao TW; He PP; Wei SC; Liu JB; Li CR; Cui Y; Yang S; Yuan WT; Li CY; Liu YF; Xu SJ; Huang W
J Invest Dermatol; 2004 May; 122(5):1121-5. PubMed ID: 15140213
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity.
Kelsell DP; Stevens HP; Ratnavel R; Bryant SP; Bishop DT; Leigh IM; Spurr NK
Hum Mol Genet; 1995 Jun; 4(6):1021-5. PubMed ID: 7544664
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
