196 related articles for article (PubMed ID: 33289110)
21. Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene.
Liu W; Wei XX; Liu JW; Habulieti X; Yang ZY; Qian YT; Ma DL
Clin Exp Dermatol; 2021 Mar; 46(2):347-348. PubMed ID: 32593192
[No Abstract] [Full Text] [Related]
22. Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsy.
Jones HF; Stoll M; Ho G; O'Neill D; Han VX; Paget S; Stewart K; Lewis J; Kothur K; Troedson C; Crow YJ; Dale RC; Mohammad SS
Brain Dev; 2022 Feb; 44(2):153-160. PubMed ID: 34702576
[TBL] [Abstract][Full Text] [Related]
23. A novel nonsense mutation of ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria.
Wu QY; Li WW; Li N; Li TF; Zhang C; Ni T; Cui YX; Li XJ; Xia XY
J Eur Acad Dermatol Venereol; 2014 Dec; 28(12):1832-3. PubMed ID: 24673593
[No Abstract] [Full Text] [Related]
24. Dyschromatosis symmetrica hereditaria.
Hayashi M; Suzuki T
J Dermatol; 2013 May; 40(5):336-43. PubMed ID: 22974014
[TBL] [Abstract][Full Text] [Related]
25. Mutations in the ADAR1 gene in Chinese families with dyschromatosis symmetrica hereditaria.
Zhang GL; Shi HJ; Shao MH; Li M; Mu HJ; Gu Y; Du XF; Xie P
Genet Mol Res; 2013 Jan; 12(3):2794-9. PubMed ID: 23315877
[TBL] [Abstract][Full Text] [Related]
26. Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.
Suzuki N; Suzuki T; Inagaki K; Ito S; Kono M; Fukai K; Takama H; Sato K; Ishikawa O; Abe M; Shimizu H; Kawai M; Horikawa T; Yoshida K; Matsumoto K; Terui T; Tsujioka K; Tomita Y
J Invest Dermatol; 2005 Jun; 124(6):1186-92. PubMed ID: 15955093
[TBL] [Abstract][Full Text] [Related]
27. Identification of two novel splice mutations of the ADAR1 gene in two Chinese families with dyschromatosis symmetrica hereditaria.
Liu H; Fu XA; Yu YX; Yu GQ; Yan XX; Liu HX; Tian HQ; Zhang FR
Clin Exp Dermatol; 2011 Oct; 36(7):797-9. PubMed ID: 21933234
[TBL] [Abstract][Full Text] [Related]
28. A novel deletion mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria.
Li WW; Wu QY; Li N; Deng DQ; Zhang RS; Cui YX; Li XJ; Xia XY
J Genet; 2014 Aug; 93(2):523-5. PubMed ID: 25189252
[No Abstract] [Full Text] [Related]
29. Novel mutations of the ADAR1 gene in two Chinese families with dyschromatosis symmetrica hereditaria.
Lv Y; Zhao Y; Xu XG; Jiang HK; Liu CX
Int J Dermatol; 2016 Oct; 55(10):e565-8. PubMed ID: 27230815
[No Abstract] [Full Text] [Related]
30. Dyschromatosis symmetrica hereditaria with chilblains due to a novel two-amino-acid deletion in the double-stranded RNA-binding domain of ADAR1.
Kono M; Suganuma M; Shimada T; Ishikura Y; Watanabe S; Takeichi T; Muro Y; Akiyama M
J Eur Acad Dermatol Venereol; 2018 Oct; 32(10):e394-e396. PubMed ID: 29775506
[No Abstract] [Full Text] [Related]
31. [Detection of ADAR1 gene mutation in a family with dyschromatosis symmetrica hereditaria].
Chang X; Ci C; Wang J; Hang S; Ji B
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):367-9. PubMed ID: 26037352
[TBL] [Abstract][Full Text] [Related]
32. [Two novel mutations of the ADAR1 gene associated with dyschromatosis symmetrica hereditaria].
Liu Y; Zhang Z; Mu Y; Xiong F; Chen X; Yang H; Yang P; Liu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):173-6. PubMed ID: 27060309
[TBL] [Abstract][Full Text] [Related]
33. Pathogenicity of ADAR1 mutation in a Chinese family with dyschromatosis symmetrica hereditaria.
Zhang SD; Feng SJ; Nh-Tseung K; Zhao JJ
J Eur Acad Dermatol Venereol; 2017 Nov; 31(11):e483-e484. PubMed ID: 28502085
[No Abstract] [Full Text] [Related]
34. A novel missense mutation in ADAR1 gene causing dyschromatosis symmetrica hereditaria in a Chinese patient.
Li ZL; Zhang GY; Hui Y; Yu RX; Li Q; Xu HX; Li CR
Indian J Dermatol Venereol Leprol; 2015; 81(3):327. PubMed ID: 25900931
[No Abstract] [Full Text] [Related]
35. Novel ADAR1 mutations in three cases of psoriasis coexisting with dyschromatosis symmetrica hereditaria.
Weng HY; Wu RW; Chen YT; Lin YF; Liu YM; Tsai SF; Chang CH
J Eur Acad Dermatol Venereol; 2022 Jan; 36(1):e54-e57. PubMed ID: 34418169
[No Abstract] [Full Text] [Related]
36. A novel frameshift mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria and the dermoscopic features.
Chi C; Luo Y; Liu J
J Eur Acad Dermatol Venereol; 2017 Nov; 31(11):e484-e485. PubMed ID: 28502110
[No Abstract] [Full Text] [Related]
37. Eleven novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria.
Kawaguchi M; Hayashi M; Murata I; Hozumi Y; Suzuki N; Ishii Y; Wataya-Kaneda M; Funasaka Y; Kawakami T; Fukai K; Ochiai T; Nishigori C; Mitsuhashi Y; Suzuki T
J Dermatol Sci; 2012 Jun; 66(3):244-5. PubMed ID: 22336994
[No Abstract] [Full Text] [Related]
38. Two novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria successfully treated with fractional CO2 laser.
Xu XG; Lv Y; Zhai JL; Li YH; Gao XH; Chen HD
J Eur Acad Dermatol Venereol; 2016 Jun; 30(6):1035-8. PubMed ID: 25763870
[No Abstract] [Full Text] [Related]
39. Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.
Liu Q; Wang Z; Wu Y; Cao L; Tang Q; Xing X; Ma H; Zhang S; Luo Y
BMC Med Genet; 2014 Jun; 15():69. PubMed ID: 24950769
[TBL] [Abstract][Full Text] [Related]
40. Dyschromatosis symmetrica hereditaria associated with neurological disorders.
Kondo T; Suzuki T; Ito S; Kono M; Negoro T; Tomita Y
J Dermatol; 2008 Oct; 35(10):662-6. PubMed ID: 19017046
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]