These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A. Krunic AL; Stone KL; Simpson MA; McGrath JA Pediatr Dermatol; 2013; 30(5):e87-8. PubMed ID: 23534700 [TBL] [Abstract][Full Text] [Related]
6. A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome. van der Velden JJ; Jonkman MF; McLean WH; Hamm H; Steijlen PM; van Steensel MA; van Geel M J Dermatol Sci; 2012 Jan; 65(1):74-6. PubMed ID: 22036214 [No Abstract] [Full Text] [Related]
7. TGM5 mutations impact epidermal differentiation in acral peeling skin syndrome. Pigors M; Kiritsi D; Cobzaru C; Schwieger-Briel A; Suárez J; Faletra F; Aho H; Mäkelä L; Kern JS; Bruckner-Tuderman L; Has C J Invest Dermatol; 2012 Oct; 132(10):2422-2429. PubMed ID: 22622422 [TBL] [Abstract][Full Text] [Related]
9. Dyskeratosis congenita with macular cutaneous amyloid deposits. Llistosella E; Moreno A; de Moragas JM Arch Dermatol; 1984 Oct; 120(10):1381-2. PubMed ID: 6486855 [No Abstract] [Full Text] [Related]
10. Acral pigmentation in alkaptonuria resembling degenerative collagenous plaques of the hands: a report of five cases. Thomas M; Jebaraj JI; Thomas M; George R J Am Acad Dermatol; 2011 Aug; 65(2):e45-e46. PubMed ID: 21763547 [No Abstract] [Full Text] [Related]
12. Acral peeling skin syndrome: a case of two brothers. Wakade O; Adams B; Shwayder T Pediatr Dermatol; 2009; 26(3):328-30. PubMed ID: 19706098 [TBL] [Abstract][Full Text] [Related]
13. Dyschromatosis: its occurrence in two Indian families with unusual features. Gharpuray MB; Tolat SN; Patwardham SP Int J Dermatol; 1994 May; 33(5):391-2. PubMed ID: 8039984 [No Abstract] [Full Text] [Related]
14. Peeling skin syndrome: genetic defects in late terminal differentiation of the epidermis. Bowden PE J Invest Dermatol; 2011 Mar; 131(3):561-4. PubMed ID: 21307953 [TBL] [Abstract][Full Text] [Related]
15. Dyschromatosis symmetrica in a Chinese with 47-XYY syndrome. Tay CH; Tock EP; Ong BH Int J Dermatol; 1972; 11(3):134-9. PubMed ID: 5039896 [No Abstract] [Full Text] [Related]
16. [Clinical contribution to the picture of idiopathic progressive atrophoderma of Pierini-Pasini]. Thiel W; Schaarschmidt H; Wätzig V Dermatol Monatsschr; 1985; 171(3):185-91. PubMed ID: 3996698 [No Abstract] [Full Text] [Related]
18. Treatment of refractory plantar fasciitis with infliximab. Eklund KK; Numminen K; Uusitalo T; Leirisalo-Repo M Scand J Rheumatol; 2007; 36(3):233-4. PubMed ID: 17657680 [No Abstract] [Full Text] [Related]
19. A novel mutation in CDSN causes peeling skin disease in a patient from Morocco. Mazereeuw-Hautier J; Leclerc EA; Simon M; Serre G; Jonca N Br J Dermatol; 2011 Nov; 165(5):1152-5. PubMed ID: 21777220 [No Abstract] [Full Text] [Related]
20. [Peeling skin disease: the responsibility of corneodesmosin]. Dereure O Ann Dermatol Venereol; 2010 Dec; 137(12):841. PubMed ID: 21134591 [No Abstract] [Full Text] [Related] [Next] [New Search]