104 related articles for article (PubMed ID: 27189830)
1. 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]
2. Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome.
Lai-Cheong JE; Sethuraman G; Ramam M; Stone K; Simpson MA; McGrath JA
Br J Dermatol; 2012 Aug; 167(2):440-2. PubMed ID: 22835024
[TBL] [Abstract][Full Text] [Related]
3. Expanding the Phenotypic Spectrum of Olmsted Syndrome.
Wilson NJ; Cole C; Milstone LM; Kiszewski AE; Hansen CD; O'Toole EA; Schwartz ME; Irwin McLean WH; Smith FJD
J Invest Dermatol; 2015 Nov; 135(11):2879-2883. PubMed ID: 26067147
[No Abstract] [Full Text] [Related]
4. Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations.
Duchatelet S; Guibbal L; de Veer S; Fraitag S; Nitschké P; Zarhrate M; Bodemer C; Hovnanian A
Br J Dermatol; 2014 Sep; 171(3):675-8. PubMed ID: 24606194
[No Abstract] [Full Text] [Related]
5. Novel p.Ala675Thr missense mutation in TRPV3 in Olmsted syndrome.
Chiu FP; Salas-Alanis JC; Amaya-Guerra M; Cepeda-Valdes R; McGrath JA; Hsu CK
Clin Exp Dermatol; 2020 Aug; 45(6):796-798. PubMed ID: 32410213
[No Abstract] [Full Text] [Related]
6. Olmsted syndrome caused by a homozygous recessive mutation in TRPV3.
Eytan O; Fuchs-Telem D; Mevorach B; Indelman M; Bergman R; Sarig O; Goldberg I; Adir N; Sprecher E
J Invest Dermatol; 2014 Jun; 134(6):1752-1754. PubMed ID: 24463422
[No Abstract] [Full Text] [Related]
7. 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]
8. Identification of a heterozygous p.Gly568Val missense mutation in the TRPV3 gene in a Japanese patient with Olmsted syndrome: In silico analysis of TRPV3.
Nagai H; Takaoka Y; Sugano A; Nakamachi Y; Kawano S; Nishigori C
J Dermatol; 2017 Sep; 44(9):1059-1062. PubMed ID: 28391651
[TBL] [Abstract][Full Text] [Related]
9. Olmsted syndrome in an Iranian boy with a new de novo mutation in TRPV3.
Kariminejad A; Barzegar M; Abdollahimajd F; Pramanik R; McGrath JA
Clin Exp Dermatol; 2014 Jun; 39(4):492-5. PubMed ID: 24758389
[TBL] [Abstract][Full Text] [Related]
10. Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in TRPV3 Gene.
Choi JY; Kim SE; Lee SE; Kim SC
Yonsei Med J; 2018 Mar; 59(2):341-344. PubMed ID: 29436206
[TBL] [Abstract][Full Text] [Related]
11. Two familial cases of Olmsted-like syndrome with a G573V mutation of the TRPV3 gene.
Zhi YP; Liu J; Han JW; Huang YP; Gao ZQ; Yang Y; Wu RN
Clin Exp Dermatol; 2016 Jul; 41(5):510-3. PubMed ID: 27273692
[TBL] [Abstract][Full Text] [Related]
12. Olmsted syndrome in an Indian male with a new de novo mutation in TRPV3.
Agarwala MK; George R; Pramanik R; McGrath JA
Br J Dermatol; 2016 Jan; 174(1):209-11. PubMed ID: 25989441
[No Abstract] [Full Text] [Related]
13. Use of Epidermal Growth Factor Receptor Inhibitor Erlotinib to Treat Palmoplantar Keratoderma in Patients With Olmsted Syndrome Caused by TRPV3 Mutations.
Greco C; Leclerc-Mercier S; Chaumon S; Doz F; Hadj-Rabia S; Molina T; Boucheix C; Bodemer C
JAMA Dermatol; 2020 Feb; 156(2):191-195. PubMed ID: 31895432
[TBL] [Abstract][Full Text] [Related]
14. Mutation in TRPV3 causes painful focal plantar keratoderma.
Peters F; Kopp J; Fischer J; Tantcheva-Poór I
J Eur Acad Dermatol Venereol; 2020 Oct; 34(10):e620-e622. PubMed ID: 32314439
[No Abstract] [Full Text] [Related]
15. TRPV3 mutants causing Olmsted Syndrome induce impaired cell adhesion and nonfunctional lysosomes.
Yadav M; Goswami C
Channels (Austin); 2017 May; 11(3):196-208. PubMed ID: 27754757
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness.
Sevior KB; Hatamochi A; Stewart IA; Bykhovskaya Y; Allen-Powell DR; Fischel-Ghodsian N; Maw MA
Am J Med Genet; 1998 Jan; 75(2):179-85. PubMed ID: 9450881
[TBL] [Abstract][Full Text] [Related]
17. A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome.
Ni C; Yan M; Zhang J; Cheng R; Liang J; Deng D; Wang Z; Li M; Yao Z
Sci Rep; 2016 Feb; 6():21815. PubMed ID: 26902751
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Olmsted syndrome: exploration of the immunological phenotype.
Danso-Abeam D; Zhang J; Dooley J; Staats KA; Van Eyck L; Van Brussel T; Zaman S; Hauben E; Van de Velde M; Morren MA; Renard M; Van Geet C; Schaballie H; Lambrechts D; Tao J; Franckaert D; Humblet-Baron S; Meyts I; Liston A
Orphanet J Rare Dis; 2013 May; 8():79. PubMed ID: 23692804
[TBL] [Abstract][Full Text] [Related]
20. [Analysis of clinical feature and genetic basis of a rare case with Olmsted syndrome].
Lu J; Hu R; Liu L; Ding H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jul; 38(7):674-677. PubMed ID: 34247376
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
