176 related articles for article (PubMed ID: 24096702)
1. Extensive postzygotic mosaicism for a novel keratin 10 mutation in epidermolytic ichthyosis.
Kiritsi D; Nanda A; Kohlhase J; Bernhard C; Bruckner-Tuderman L; Happle R; Has C
Acta Derm Venereol; 2014 May; 94(3):346-8. PubMed ID: 24096702
[No Abstract] [Full Text] [Related]
2. Extensive Post-zygotic Mosaicism of KRT1 or KRT10 Mutation Mimicking Classical Epider-molytic Ichthyosis.
Severino-Freire M; Jonca N; Pichery M; Tournier E; Chassaing N; Mazereeuw-Hautier J
Acta Derm Venereol; 2017 Mar; 97(3):387-388. PubMed ID: 27722766
[No Abstract] [Full Text] [Related]
3. Epidermolytic Ichthyosis Sine Epidermolysis.
Eskin-Schwartz M; Drozhdina M; Sarig O; Gat A; Jackman T; Isakov O; Shomron N; Samuelov L; Malchin N; Peled A; Vodo D; Hovnanian A; Ruzicka T; Koshkin S; Harmon RM; Koetsier JL; Green KJ; Paller AS; Sprecher E
Am J Dermatopathol; 2017 Jun; 39(6):440-444. PubMed ID: 28121638
[TBL] [Abstract][Full Text] [Related]
4. Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis.
Hotz A; Oji V; Bourrat E; Jonca N; Mazereeuw-Hautier J; Betz RC; Blume-Peytavi U; Stieler K; Morice-Picard F; Schönbuchner I; Markus S; Schlipf N; Fischer J
Acta Derm Venereol; 2016 May; 96(4):473-8. PubMed ID: 26581228
[TBL] [Abstract][Full Text] [Related]
5. Mild phenotype of epidermolytic hyperkeratosis mimicking ichthyosis bullosa of Siemens is related to specific mutation in 2B domain of KRT1.
Sung JY; Oh SW; Kim SE; Kim SC
J Dermatol Sci; 2013 Jun; 70(3):220-2. PubMed ID: 23623204
[No Abstract] [Full Text] [Related]
6. Generalized and naevoid epidermolytic ichthyosis in Denmark: clinical and mutational findings.
Bygum A; Virtanen M; Brandrup F; GĂ„nemo A; Sommerlund M; Strauss G; Vahlquist A
Acta Derm Venereol; 2013 May; 93(3):309-13. PubMed ID: 22930352
[TBL] [Abstract][Full Text] [Related]
7. Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation location.
Vodo D; Sarig O; Peled A; Samuelov L; Malchin N; Grafi-Cohen M; Sprecher E
Clin Exp Dermatol; 2018 Mar; 43(2):187-190. PubMed ID: 29277919
[TBL] [Abstract][Full Text] [Related]
8. Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis.
Takemoto K; Makino T; Mizawa M; Kubo Y; Shimizu T
Eur J Dermatol; 2019 Apr; 29(2):227-228. PubMed ID: 31106763
[No Abstract] [Full Text] [Related]
9. [Generalized skin change in a newborn infant: infectious, genetic or autoimmune cause? Epidermolytic ichthyosis].
Jaeger J; Andres C; Grosber M; Suarez IL; Zirbs M; Ring J; Brockow K
MMW Fortschr Med; 2013 Mar; 155(4):5, 72. PubMed ID: 23614180
[No Abstract] [Full Text] [Related]
10. Generalized epidermolytic hyperkeratosis in two unrelated children from parents with localized linear form, and prenatal diagnosis.
Chassaing N; Kanitakis J; Sportich S; Cordier-Alex MP; Titeux M; Calvas P; Claudy A; Berbis P; Hovnanian A
J Invest Dermatol; 2006 Dec; 126(12):2715-7. PubMed ID: 16990804
[No Abstract] [Full Text] [Related]
11. Epidermolytic Acanthoma of the Genitalia Does Not Show Mutations in KRT1 or KRT10.
Egozi-Reinman E; Avitan-Hersh E; Barzilai A; Indelman M; Bergman R
Am J Dermatopathol; 2016 Feb; 38(2):164-5. PubMed ID: 26825163
[No Abstract] [Full Text] [Related]
12. R156C mutation of keratin 10 causes mild form of epidermolytic hyperkeratosis.
Haruna K; Suga Y; Mizuno Y; Hasegawa T; Kourou K; Matsuba S; Muramatsu S; Ikeda S
J Dermatol; 2007 Aug; 34(8):545-8. PubMed ID: 17683385
[TBL] [Abstract][Full Text] [Related]
13. Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10.
Covaciu C; Castori M; De Luca N; Ghirri P; Nannipieri A; Ragone G; Zambruno G; Castiglia D
Br J Dermatol; 2010 Jun; 162(6):1384-7. PubMed ID: 20302579
[TBL] [Abstract][Full Text] [Related]
14. Localized linear epidermolytic epidermal nevus of male genitalia with a recurrent keratin 10 mutation, p.Arg156His.
Uchiyama K; Nakanishi G; Fujimoto N; Takikita M; Tanaka T
Eur J Dermatol; 2013; 23(4):557-8. PubMed ID: 24001792
[No Abstract] [Full Text] [Related]
15. Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia.
Yamamoto M; Tsuda T; Otaki Y; Nakanishi T; Yamanishi K
J Dermatol; 2012 Aug; 39(8):716-8. PubMed ID: 22035476
[No Abstract] [Full Text] [Related]
16. A case of epidermolytic ichthyosis showing a very mild phenotype due to a novel tail extension mutation in KRT10.
Kono M; Fukai K; Omura R; Sugawara K; Tsuruta D; Sugiura K; Akiyama M
J Eur Acad Dermatol Venereol; 2017 Feb; 31(2):e68-e69. PubMed ID: 27225831
[No Abstract] [Full Text] [Related]
17. Ichthyosis with Confetti Inherited from a Mosaic Father.
Pallesen KAU; Clemmensen O; Fischer J; Hertz JM; Bygum A
Acta Derm Venereol; 2018 Jan; 98(1):130-131. PubMed ID: 29135017
[No Abstract] [Full Text] [Related]
18. Epidcermolytic hyperkeratosis: a case report.
Achar A; Naskar B; Laha R; Ray S
J Indian Med Assoc; 2009 Mar; 107(3):171-2. PubMed ID: 19810387
[TBL] [Abstract][Full Text] [Related]
19. Superficial epidermolytic ichthyosis: a report of two families.
Cervantes T; Pham C; Browning JC
Pediatr Dermatol; 2013; 30(4):469-72. PubMed ID: 22612346
[TBL] [Abstract][Full Text] [Related]
20. A case of epidermolytic hyperkeratosis with no facial involvement associated with mutation in keratin 10.
Ishii N; Hamada T; Yasumoto S; Hashimoto T
Clin Exp Dermatol; 2008 May; 33(3):353-4. PubMed ID: 18261139
[No Abstract] [Full Text] [Related]
[Next] [New Search]