139 related articles for article (PubMed ID: 28884927)
1. Peeling skin syndrome associated with novel variant in FLG2 gene.
Alfares A; Al-Khenaizan S; Al Mutairi F
Am J Med Genet A; 2017 Dec; 173(12):3201-3204. PubMed ID: 28884927
[TBL] [Abstract][Full Text] [Related]
2. Generalized Ichthyotic Peeling Skin Syndrome due to FLG2 Mutations.
Bolling MC; Jan SZ; Pasmooij AMG; Lemmink HH; Franke LH; Yenamandra VK; Sinke RJ; van den Akker PC; Jonkman MF
J Invest Dermatol; 2018 Aug; 138(8):1881-1884. PubMed ID: 29505760
[No Abstract] [Full Text] [Related]
3. Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A.
Mohamad J; Sarig O; Godsel LM; Peled A; Malchin N; Bochner R; Vodo D; Rabinowitz T; Pavlovsky M; Taiber S; Fried M; Eskin-Schwartz M; Assi S; Shomron N; Uitto J; Koetsier JL; Bergman R; Green KJ; Sprecher E
J Invest Dermatol; 2018 Aug; 138(8):1736-1743. PubMed ID: 29758285
[TBL] [Abstract][Full Text] [Related]
4. Generalized Skin Scaling in a Young Girl: A Quiz.
Mo R; Wang H; Lin Z
Acta Derm Venereol; 2019 Dec; 99(13):1322-1323. PubMed ID: 31612237
[No Abstract] [Full Text] [Related]
5. A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.
Gordon H; Yap P; Hsiao KC; Watson M; Purvis D
Pediatr Dermatol; 2022 Mar; 39(2):268-272. PubMed ID: 35178752
[TBL] [Abstract][Full Text] [Related]
6. Homozygous deletion of six genes including corneodesmosin on chromosome 6p21.3 is associated with generalized peeling skin disease.
Teye K; Hamada T; Krol RP; Numata S; Ishii N; Matsuda M; Ohata C; Furumura M; Hashimoto T
J Dermatol Sci; 2014 Jul; 75(1):36-42. PubMed ID: 24794518
[TBL] [Abstract][Full Text] [Related]
7. Inflammatory peeling skin syndrome caused by homozygous genomic deletion in the PSORS1 region encompassing the CDSN gene.
Ishida-Yamamoto A; Furio L; Igawa S; Honma M; Tron E; Malan V; Murakami M; Hovnanian A
Exp Dermatol; 2014 Jan; 23(1):60-3. PubMed ID: 24372652
[TBL] [Abstract][Full Text] [Related]
8. PLACK syndrome shows remarkable phenotypic homogeneity.
Mohamad J; Samuelov L; Ben-Amitai D; Malchin N; Sarig O; Sprecher E
Clin Exp Dermatol; 2019 Jul; 44(5):580-583. PubMed ID: 30656735
[No Abstract] [Full Text] [Related]
9. Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.
Mohamad J; Nanda A; Pavlovsky M; Peled A; Malchin N; Malovitski K; Pramanik R; Weissglas-Volkov D; Shomron N; McGrath J; Sprecher E; Sarig O
Exp Dermatol; 2020 Aug; 29(8):742-748. PubMed ID: 32618001
[TBL] [Abstract][Full Text] [Related]
10. Genetic heterogeneity in keratolytic winter erythema (Oudtshoorn skin disease).
Huntington MK; Jassim AD
Arch Dermatol; 2006 Aug; 142(8):1073-4. PubMed ID: 16924068
[No Abstract] [Full Text] [Related]
11. Peeling skin syndrome.
Bansal M; Mahajan S; Sankhwar S; Bansal A
BMJ Case Rep; 2015 Jul; 2015():. PubMed ID: 26150647
[No Abstract] [Full Text] [Related]
12. Alu-mediated large deletion of the CDSN gene as a cause of peeling skin disease.
Wada T; Matsuda Y; Muraoka M; Toma T; Takehara K; Fujimoto M; Yachie A
Clin Genet; 2014 Oct; 86(4):383-6. PubMed ID: 24116970
[TBL] [Abstract][Full Text] [Related]
13. Painless erosions on the hands and feet of a 7-year-old boy.
Schimmel J; Renzi M; Fawaz B; Halpern A
Pediatr Dermatol; 2020 Mar; 37(2):371-372. PubMed ID: 32196738
[No Abstract] [Full Text] [Related]
14. 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]
15. A novel homozygous nonsense mutation in CAST associated with PLACK syndrome.
Temel ŞG; Karakaş B; Şeker Ü; Turkgenç B; Zorlu Ö; Sarıcaoğlu H; Oğur Ç; Kütük Ö; Kelsell DP; Yakıcıer MC
Cell Tissue Res; 2019 Nov; 378(2):267-277. PubMed ID: 31392520
[TBL] [Abstract][Full Text] [Related]
16. Peeling skin syndrome in eight cases of four different families from India and Bangladesh.
Sarma N; Boler AK; Bhanja DC
Indian J Dermatol Venereol Leprol; 2012; 78(5):625-31. PubMed ID: 22960820
[TBL] [Abstract][Full Text] [Related]
17. The glycan-specific sulfotransferase (R77W)GalNAc-4-ST1 putatively responsible for peeling skin syndrome has normal properties consistent with a simple sequence polymorphisim.
Fiete D; Mi Y; Beranek M; Baenziger NL; Baenziger JU
Glycobiology; 2017 May; 27(5):450-456. PubMed ID: 28204496
[TBL] [Abstract][Full Text] [Related]
18. Identification of the first nonsense CDSN mutation with expression of a truncated protein causing peeling skin syndrome type B.
Mallet A; Kypriotou M; George K; Leclerc E; Rivero D; Mazereeuw-Hautier J; Serre G; Huber M; Jonca N; Hohl D
Br J Dermatol; 2013 Dec; 169(6):1322-5. PubMed ID: 23957618
[TBL] [Abstract][Full Text] [Related]
19. Increased expression of epidermal thymic stromal lymphopoietin in inflammatory peeling skin syndrome.
Wada T; Toma T; Hamaguchi Y; Yachie A
J Dermatol; 2014 May; 41(5):448-9. PubMed ID: 24628284
[No Abstract] [Full Text] [Related]
20. A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases.
Teye K; Suga Y; Numata S; Soejima M; Ishii N; Krol RP; Ohata C; Matsuda M; Honma M; Ishida-Yamamoto A; Hamada T; Koda Y; Hashimoto T
J Dermatol Sci; 2016 May; 82(2):134-7. PubMed ID: 26867961
[No Abstract] [Full Text] [Related]
[Next] [New Search]