222 related articles for article (PubMed ID: 26902751)
21. Genotype‒Phenotype Correlation of TRPV3-Related Olmsted Syndrome.
Zhong W; Hu L; Cao X; Zhao J; Zhang X; Lee M; Wang H; Zhang J; Chen Q; Feng C; Duo L; Wang X; Tang L; Lin Z; Yang Y
J Invest Dermatol; 2021 Mar; 141(3):545-554. PubMed ID: 32795529
[TBL] [Abstract][Full Text] [Related]
22. Olmsted syndrome--congenital palmoplantar and periorificial keratoderma.
Poulin Y; Perry HO; Muller SA
J Am Acad Dermatol; 1984 Apr; 10(4):600-10. PubMed ID: 6232300
[TBL] [Abstract][Full Text] [Related]
23. SMARCAD1 Haploinsufficiency Underlies Huriez Syndrome and Associated Skin Cancer Susceptibility.
Günther C; Lee-Kirsch MA; Eckhard J; Matanovic A; Kerscher T; Rüschendorf F; Klein B; Berndt N; Zimmermann N; Flachmeier C; Thuß T; Lucas N; Marenholz I; Esparza-Gordillo J; Hübner N; Traupe H; Delaporte E; Lee YA
J Invest Dermatol; 2018 Jun; 138(6):1428-1431. PubMed ID: 29409814
[No Abstract] [Full Text] [Related]
24. Nonmutilating palmoplantar and periorificial kertoderma: a variant of Olmsted syndrome or a distinct entity?
Nofal A; Assaf M; Nassar A; Nofal E; Shehab M; El-Kabany M
Int J Dermatol; 2010 Jun; 49(6):658-65. PubMed ID: 20618471
[TBL] [Abstract][Full Text] [Related]
25. Olmsted syndrome: mutilating palmoplantar keratoderma with periorificial keratotic plaques.
Mevorah B; Goldberg I; Sprecher E; Bergman R; Metzker A; Luria R; Gat A; Brenner S
J Am Acad Dermatol; 2005 Nov; 53(5 Suppl 1):S266-72. PubMed ID: 16227106
[No Abstract] [Full Text] [Related]
26. Palmoplantar keratoderma and perioral keratotic plaques with hypotrichosis in a child.
Zhang LW; Wang WJ; Chen T; Fu LX; Lu YH
Pediatr Dermatol; 2019 Nov; 36(6):942-943. PubMed ID: 31778560
[No Abstract] [Full Text] [Related]
27. Recent advances in intraepidermal blistering diseases.
Devries DT; Warren SJ
Adv Dermatol; 2002; 18():203-45. PubMed ID: 12528407
[No Abstract] [Full Text] [Related]
28. [Progressive symmetric erythrokeratodermia of Darier-Gottron].
Ott H; Lehmann S; Poblete-Gutiérrez P; Frank J
Hautarzt; 2004 Oct; 55(10):994-6. PubMed ID: 15340705
[TBL] [Abstract][Full Text] [Related]
29. Olmsted syndrome: report of two new cases and literature review.
Larrègue M; Callot V; Kanitakis J; Suau AM; Foret M
J Dermatol; 2000 Sep; 27(9):557-68. PubMed ID: 11052230
[TBL] [Abstract][Full Text] [Related]
30. [Familial palmo-plantar keratoderma with epidermolytic hyperkeratosis (author's transl)].
Moulin G; Bouchet R
Ann Dermatol Venereol; 1977 Jan; 104(1):38-44. PubMed ID: 14586
[TBL] [Abstract][Full Text] [Related]
31. Semidominant Inheritance in Olmsted Syndrome.
Cao X; Wang H; Li Y; Lee M; Jiang L; Zhou Y; Feng C; Lin Z; Yang Y
J Invest Dermatol; 2016 Aug; 136(8):1722-1725. PubMed ID: 27189830
[No Abstract] [Full Text] [Related]
32. Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes.
Song Z; Chen X; Zhao Q; Stanic V; Lin Z; Yang S; Chen T; Chen J; Yang Y
J Invest Dermatol; 2021 Aug; 141(8):1964-1974. PubMed ID: 33675791
[TBL] [Abstract][Full Text] [Related]
33. Olmsted Syndrome in a Family.
Konathan R; Alur SK
Int J Trichology; 2016; 8(4):168-170. PubMed ID: 28442872
[TBL] [Abstract][Full Text] [Related]
34. A novel missense mutation of the ATP2A2 gene in a Chinese family with Darier's disease.
Yang S; Sun LD; Liu HS; Wang JY; He PP; Li M; Gao M; Liu JB; Yang J; Wang ZX; Zhu YY; Lin D; Zhang XJ
Arch Dermatol Res; 2004 Jun; 296(1):21-4. PubMed ID: 15095095
[TBL] [Abstract][Full Text] [Related]
35. Focal palmoplantar and gingival keratosis: a distinct palmoplantar ectodermal dysplasia with epidermolytic alterations but lack of mutations in known keratins.
Kolde G; Hennies HC; Bethke G; Reichart PA
J Am Acad Dermatol; 2005 Mar; 52(3 Pt 1):403-9. PubMed ID: 15761417
[TBL] [Abstract][Full Text] [Related]
36. Novel VPS33B mutation in a patient with autosomal recessive keratoderma-ichthyosis-deafness syndrome.
Alter S; Hotz A; Jahn A; Di Donato N; Schröck E; Smitka M; von der Hagen M; Schallner J; Menschikowski M; Gillitzer C; Laass MW; Fischer J; Tzschach A
Am J Med Genet A; 2018 Dec; 176(12):2862-2866. PubMed ID: 30561130
[TBL] [Abstract][Full Text] [Related]
37. Olmsted syndrome with squamous cell carcinoma of extremities and adenocarcinoma of the lung: failure to detect loricrin gene mutation.
Ogawa F; Udono M; Murota H; Shimizu K; Takahashi H; Ishida-Yamamoto A; Iizuka H; Katayama I
Eur J Dermatol; 2003; 13(6):524-8. PubMed ID: 14721769
[TBL] [Abstract][Full Text] [Related]
38. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression from mutations of R75W and R75Q in the GJB2 gene.
Birkenhäger R; Lüblinghoff N; Prera E; Schild C; Aschendorff A; Arndt S
Am J Med Genet A; 2010 Jul; 152A(7):1798-802. PubMed ID: 20583176
[TBL] [Abstract][Full Text] [Related]
39. [Familial coexistence of erythrokeratodermia variabilis and keratosis palmoplantaris transgrediens et progrediens].
Wollina U; Knopf B; Schaaschmidt H; Frille I
Hautarzt; 1989 Mar; 40(3):169-72. PubMed ID: 2523877
[TBL] [Abstract][Full Text] [Related]
40. A novel 5-bp deletion mutation in AAGAB gene in a Chinese family with punctate palmoplantar keratoderma.
Li M; Dai X; Cheng R; Yang L; Yao Z; Liu J
Acta Derm Venereol; 2014 May; 94(3):339-40. PubMed ID: 24162853
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
