These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 18331298)

  • 41. First report of the coexistence of dyschromatosis symmetrica hereditaria and psoriasis: one novel TCT to A mutation in the double-RNA-specific adenosine deaminase gene.
    Shi BJ; Xue M; Liu Y; Jiang Y; Diao QC
    J Eur Acad Dermatol Venereol; 2012 May; 26(5):657-8. PubMed ID: 21564324
    [No Abstract]   [Full Text] [Related]  

  • 42. Dyschromatosis symmetrica hereditaria: report of a sporadic case.
    Consigli J; Zanni MS; Ragazzini L; Danielo C
    Int J Dermatol; 2010 Aug; 49(8):918-20. PubMed ID: 21128916
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. 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]  

  • 45. Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes.
    Kondo T; Suzuki T; Mitsuhashi Y; Ito S; Kono M; Komine M; Akita H; Tomita Y
    J Dermatol; 2008 Jul; 35(7):395-406. PubMed ID: 18705826
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Eight Novel Mutations of the ADAR1 Gene in Chinese Patients with Dyschromatosis Symmetrica Hereditaria.
    Tang ZL; Wang S; Tu C; Wang T; Ma CW; Liu Y; Xiao SX; Wang XP
    Genet Test Mol Biomarkers; 2018 Feb; 22(2):104-108. PubMed ID: 29185800
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Mutation analysis of the ADAR1 gene in a Chinese Family with dyschromatosis symmetrica hereditaria.
    Huang Y; Zhao X; Mei Q; Cheng B; Zhao Y; Shangguan Z
    Australas J Dermatol; 2014 Feb; 55(1):92-3. PubMed ID: 24433377
    [No Abstract]   [Full Text] [Related]  

  • 48. 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]  

  • 49. Novel de novo heterozygous frameshift mutation of the ADAR1 gene in heavy dyschromatosis symmetrica hereditaria.
    Li CR; Li H; Yu RX; Li ZL; Li Q; Gong JQ
    Cutis; 2016 Sep; 98(3):E16-E18. PubMed ID: 27814417
    [No Abstract]   [Full Text] [Related]  

  • 50. Dermoscopic features in a case of dyschromatosis symmetrica hereditaria.
    Oiso N; Murata I; Hayashi M; Amatsu A; Yoshida M; Suzuki T; Kawada A
    J Dermatol; 2011 Jan; 38(1):91-3. PubMed ID: 21175763
    [No Abstract]   [Full Text] [Related]  

  • 51. A novel complex insertion-deletion mutation in ADAR1 gene in a Chinese family with dyschromatosis symmetrica hereditaria.
    Li M; Jin C; Yang L; Lai M; Yao Z
    J Eur Acad Dermatol Venereol; 2011 Jun; 25(6):743-6. PubMed ID: 20586835
    [No Abstract]   [Full Text] [Related]  

  • 52. Dyschromatosis symmetrica hereditaria--a histochemical and ultrastructural study.
    Sheu HM; Yu HS
    Taiwan Yi Xue Hui Za Zhi; 1985 Feb; 84(2):238-49. PubMed ID: 3925074
    [No Abstract]   [Full Text] [Related]  

  • 53. Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family.
    Sandhu K; Saraswat A; Kanwar AJ
    J Eur Acad Dermatol Venereol; 2004 Nov; 18(6):702-4. PubMed ID: 15482301
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Acral dyschromatosis with developmental regression and dystonia in a seven-year-old child: dyschromatosis symmetrica hereditaria variant or a new syndrome?
    Kaliyadan F; Vinayan KP; Fernandes B; Jayasree MG
    Indian J Dermatol Venereol Leprol; 2009; 75(4):412-4. PubMed ID: 19584476
    [No Abstract]   [Full Text] [Related]  

  • 55. Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9.
    Kono M; Miyamura Y; Matsunaga J; Tomita Y
    J Dermatol Sci; 2000 Feb; 22(2):88-95. PubMed ID: 10674821
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Dyschromatosis symmetrica hereditaria.
    Hayashi M; Suzuki T
    J Dermatol; 2013 May; 40(5):336-43. PubMed ID: 22974014
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?
    Kono M; Akiyama M; Suganuma M; Tomita Y; Sanchez-Valle A
    Int J Dermatol; 2013 Dec; 52(12):1582-4. PubMed ID: 24261734
    [No Abstract]   [Full Text] [Related]  

  • 58. A novel splice site mutation in the ADAR gene leading to exon skipping and dyschromatosis symmetrica hereditaria in a Japanese patient.
    Ansai O; Shigehara Y; Ito A; Abe R; Shimomura Y
    Clin Exp Dermatol; 2016 Dec; 41(8):933-934. PubMed ID: 27747905
    [No Abstract]   [Full Text] [Related]  

  • 59. [The c.3463C>T mutation of the ADAR1 gene in patients with dyschromatosis symmetrical hereditaria].
    Song J; Zhou H; Lu RQ; Zhang LP; Sun H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):576-8. PubMed ID: 20931541
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Genetics of pigmentary disorders.
    Tomita Y; Suzuki T
    Am J Med Genet C Semin Med Genet; 2004 Nov; 131C(1):75-81. PubMed ID: 15452859
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.