311 related articles for article (PubMed ID: 17635506)
21. Assessment of melanin distribution in epidermolysis bullosa simplex with mottled pigmentation: A case report.
Chao JP; Lin JY; Chiang CY; Hsieh TS; Lin SJ; Hong JB
J Dermatol; 2022 Feb; 49(2):e63-e64. PubMed ID: 34873742
[No Abstract] [Full Text] [Related]
22. Novel de novo mutation in KRT14 underlies a localized form of epidermolysis bullosa simplex.
Ołdak M; Przybylska D; Kosińska J; Federowicz A; Woźniak K; Płoski R; Kowalewski C
Eur J Dermatol; 2013; 23(3):404-6. PubMed ID: 23774754
[No Abstract] [Full Text] [Related]
23. Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.
Müller FB; Küster W; Wodecki K; Almeida H; Bruckner-Tuderman L; Krieg T; Korge BP; Arin MJ
Hum Mutat; 2006 Jul; 27(7):719-20. PubMed ID: 16786515
[TBL] [Abstract][Full Text] [Related]
24. A novel homozygous keratin 14 mutation in a patient with autosomal recessive epidermolysis bullosa simplex and squamous cell carcinoma of the tongue.
Baek JO; Lee HY; Oh SW; Lee JS; Kim SC; Lee JR; Roh JY
Br J Dermatol; 2010 Apr; 162(4):880-2. PubMed ID: 20096008
[No Abstract] [Full Text] [Related]
25. Novel keratin 14 hotspot mutation in Dowling-Meara type of epidermolysis bullosa simplex: strategy to avoid KRT14 pseudogene amplification by a simple approach.
Ołdak M; Kowalewski C; Maksym RB; Woźniak K; Pollak A; Podgórska M; Wnorowski A; Kosińska J; Płoski R
J Dermatol Sci; 2010 Jan; 57(1):69-70. PubMed ID: 19854623
[No Abstract] [Full Text] [Related]
26. Epidermolysis bullosa simplex in Japanese and Korean patients: genetic studies in 19 cases.
Yasukawa K; Sawamura D; Goto M; Nakamura H; Jung SY; Kim SC; Shimizu H
Br J Dermatol; 2006 Aug; 155(2):313-7. PubMed ID: 16882168
[TBL] [Abstract][Full Text] [Related]
27. [Epidermolysis bullosa simplex Dowling-Meara].
Frangu M; Gedde-Dahl T; Verder H
Ugeskr Laeger; 2006 Nov; 168(48):4222-4. PubMed ID: 17147951
[TBL] [Abstract][Full Text] [Related]
28. A new mutation in the linker 12 domain of keratin 5 in a Chinese family with Weber-Cockayne epidermolysis bullosa simplex.
Li JG; Feng J; Xiao SX; Ai YL; Wang JM; Peng ZH
Clin Exp Dermatol; 2004 Sep; 29(5):539-41. PubMed ID: 15347343
[TBL] [Abstract][Full Text] [Related]
29. Digenic inheritance of KRT5 and KRT14 mutations in a family with epidermolysis bullosa simplex.
Yu Y; Mi Z; Fu X; Wang Z; Sun L; Liu H; Zhang F
Australas J Dermatol; 2020 May; 61(2):e267-e269. PubMed ID: 31919841
[No Abstract] [Full Text] [Related]
30. Digenic inheritance in epidermolysis bullosa simplex.
Padalon-Brauch G; Ben Amitai D; Vodo D; Harel A; Sarig O; Sprecher E; Mashiah J
J Invest Dermatol; 2012 Dec; 132(12):2852-4. PubMed ID: 22832485
[No Abstract] [Full Text] [Related]
31. Epidermolysis bullosa simplex with mottled pigmentation: a family report and review.
Echeverría-García B; Vicente A; Hernández Á; Mascaró JM; Colmenero I; Terrón A; Escámez MJ; del Río M; González-Enseñat MA; Torrelo A
Pediatr Dermatol; 2013; 30(6):e125-31. PubMed ID: 22640275
[TBL] [Abstract][Full Text] [Related]
32. Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia: identification of a recurrent p.P25L mutation in KRT5 in four affected family members.
Nagai H; Oiso N; Tomida S; Sakai K; Fujiwara S; Nakamachi Y; Kawano S; Kawada A; Nishio K; Nishigori C
Br J Dermatol; 2016 Mar; 174(3):633-5. PubMed ID: 26286811
[No Abstract] [Full Text] [Related]
33. Association of Epidermolysis Bullosa Simplex With Mottled Pigmentation and EXPH5 Mutations.
Turcan I; Pasmooij AM; Van den Akker PC; Lemmink H; Sinke RJ; Jonkman MF
JAMA Dermatol; 2016 Oct; 152(10):1137-1141. PubMed ID: 27384765
[TBL] [Abstract][Full Text] [Related]
34. Novel keratin 5 and 14 gene mutations in patients with epidermolysis bullosa simplex from Poland.
Hamada T; Kawano Y; Szczecinska W; Wozniak K; Yasumoto S; Kowalewski C; Hashimoto T
Arch Dermatol Res; 2005 Jun; 296(12):577-9. PubMed ID: 15827748
[TBL] [Abstract][Full Text] [Related]
35. Digenic inheritance in epidermolysis bullosa simplex involving two novel mutations in KRT5 and KRT14.
Kim E; Harris A; Hyland V; Murrell DF
Br J Dermatol; 2017 Jul; 177(1):262-264. PubMed ID: 27611893
[No Abstract] [Full Text] [Related]
36. Autosomal recessive epidermolysis bullosa simplex due to KRT14 mutation: two large Palestinian families and literature review.
Diociaiuti A; Castiglia D; Naim M; Condorelli AG; Zambruno G; El Hachem M
J Eur Acad Dermatol Venereol; 2018 Apr; 32(4):e149-e151. PubMed ID: 29024068
[No Abstract] [Full Text] [Related]
37. Utilization of a cryptic noncanonical donor splice site in the KRT14 gene causes a mild form of epidermolysis bullosa simplex.
Han S; Cooper DN; Bowden PE
Br J Dermatol; 2006 Jul; 155(1):201-3. PubMed ID: 16792776
[No Abstract] [Full Text] [Related]
38. Epidermolysis bullosa simplex with mottled pigmentation: a case report.
Andres C; Chen W; Hofmann H; Ring J; Schnopp C
Int J Dermatol; 2009 Jul; 48(7):753-4. PubMed ID: 19570085
[No Abstract] [Full Text] [Related]
39. Missense mutation at the helix termination region in the 2B domain of keratin 14 in a Japanese family with epidermolysis bullosa simplex, generalized, other.
Kaneko S; Hamada T; Kawano Y; Hashimoto T; Morita E
Int J Dermatol; 2011 Apr; 50(4):436-8. PubMed ID: 21413954
[No Abstract] [Full Text] [Related]
40. Mutation screening of entire keratin 5 and keratin 14 genes and identification of a novel mutation in a Chinese family with epidermolysis bullosa simplex Dowling-Meara.
Yuan H; Liu F; Xiao B; He Y; Liang Y; Liu J
J Eur Acad Dermatol Venereol; 2008 Dec; 22(12):1510-2. PubMed ID: 18384561
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
