176 related articles for article (PubMed ID: 35887135)
1. Deep Phenotyping of Superficial Epidermolytic Ichthyosis due to a Recurrent Mutation in
Suzuki Y; Takeichi T; Tanahashi K; Muro Y; Suga Y; Ogi T; Akiyama M
Int J Mol Sci; 2022 Jul; 23(14):. PubMed ID: 35887135
[TBL] [Abstract][Full Text] [Related]
2. The first case of a mosaic superficial epidermolytic ichthyosis diagnosed by Ultra-Deep Sequence.
Li Y; Cheng R; Liang J; Yao Z; Li M
Mol Genet Genomic Med; 2020 Nov; 8(11):e1457. PubMed ID: 32881395
[TBL] [Abstract][Full Text] [Related]
3. First Case of
Diociaiuti A; Castiglia D; Corbeddu M; Rotunno R; Rossi S; Pisaneschi E; Cesario C; Condorelli AG; Zambruno G; El Hachem M
Int J Mol Sci; 2020 Oct; 21(20):. PubMed ID: 33081034
[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. Epidermolytic epidermal nevus caused by a somatic mutation in KRT2.
Mohamad J; Samuelov L; Assaf S; Vodo D; Sarig O; Sprecher E
Pediatr Dermatol; 2021 Mar; 38(2):538-540. PubMed ID: 33555633
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Superficial epidermolytic ichthyosis caused by a novel KRT2 mutation.
Akasaka E; Minakawa S; Rokunohe D; Toyomaki Y; Matsuzaki Y; Sawamura D; Nakano H
J Dermatol Sci; 2015 Jul; 79(1):86-8. PubMed ID: 25979451
[No Abstract] [Full Text] [Related]
8. Scabies in a 14-year-old girl with superficial epidermolytic ichthyosis.
Vázquez-Osorio I; Moreiras-Arias N; Pérez-Feal P; Sainz-Gaspar L; Ortiz-Cabrera NV; Hernández-Martín A
Pediatr Dermatol; 2022 Mar; 39(2):305-306. PubMed ID: 34779035
[TBL] [Abstract][Full Text] [Related]
9. [Clinical presentation and etiology of ichthyoses. Overview of the new nomenclature and classification].
Oji V
Hautarzt; 2010 Oct; 61(10):891-902; quiz 903-4. PubMed ID: 20827455
[TBL] [Abstract][Full Text] [Related]
10. Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma.
Smith FJD; Kreuser-Genis IM; Jury CS; Wilson NJ; Terron-Kwiatowski A; Zamiri M
Clin Exp Dermatol; 2019 Jul; 44(5):528-534. PubMed ID: 30288772
[TBL] [Abstract][Full Text] [Related]
11. Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literature.
Basarab T; Smith FJ; Jolliffe VM; McLean WH; Neill S; Rustin MH; Eady RA
Br J Dermatol; 1999 Apr; 140(4):689-95. PubMed ID: 10233323
[TBL] [Abstract][Full Text] [Related]
12. Clinical and genetic findings in 13 Chinese children with keratinopathic ichthyosis.
Yang Z; Xu Z; He R; Xiang X; Zhang B; Ma L
Pediatr Investig; 2023 Sep; 7(3):168-176. PubMed ID: 37736367
[TBL] [Abstract][Full Text] [Related]
13. Mutations in KRT10 in epidermolytic acanthoma.
Cheraghlou S; Atzmony L; Roy SF; McNiff JM; Choate KA
J Cutan Pathol; 2020 Jun; 47(6):524-529. PubMed ID: 32045015
[TBL] [Abstract][Full Text] [Related]
14. A glutamate to lysine mutation at the end of 2B rod domain of keratin 2e gene in ichthyosis bullosa of Siemens.
Yang JM; Lee ES; Kang HJ; Choi GS; Yoneda K; Jung SY; Park KB; Steinert PM; Lee ES
Acta Derm Venereol; 1998 Nov; 78(6):417-9. PubMed ID: 9833038
[TBL] [Abstract][Full Text] [Related]
15. Intrafamilial phenotypic heterogeneity of epidermolytic ichthyosis associated with a new missense mutation in keratin 10.
Abdul-Wahab A; Takeichi T; Liu L; Stephens C; Akiyama M; McGrath JA
Clin Exp Dermatol; 2016 Apr; 41(3):290-3. PubMed ID: 26338057
[TBL] [Abstract][Full Text] [Related]
16. Inherited ichthyosis: Non-syndromic forms.
Takeichi T; Akiyama M
J Dermatol; 2016 Mar; 43(3):242-51. PubMed ID: 26945532
[TBL] [Abstract][Full Text] [Related]
17. Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene.
Moraru R; Cserhalmi-Friedman PB; Grossman ME; Schneiderman P; Christiano AM
Clin Exp Dermatol; 1999 Sep; 24(5):412-5. PubMed ID: 10564334
[TBL] [Abstract][Full Text] [Related]
18. Infantile epidermolytic ichthyosis with prominent maternal palmoplantar keratoderma.
Austin Smith W; Cope A; Fernandez M; Parekh P
Dermatol Online J; 2016 Apr; 22(4):. PubMed ID: 27617465
[TBL] [Abstract][Full Text] [Related]
19. Epidermolytic hyperkeratosis: applied molecular genetics.
DiGiovanna JJ; Bale SJ
J Invest Dermatol; 1994 Mar; 102(3):390-4. PubMed ID: 7509838
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
