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 *

88 related articles for article (PubMed ID: 3925074)

  • 21. 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]  

  • 22. Dyschromatosis symmetrica hereditaria: a case report from Turkey, a new association and a novel gene mutation.
    Bilen N; Aktürk AŞ; Kawaguchi M; Salman S; Erçin C; Hozumi Y; Suzuki T
    J Dermatol; 2012 Oct; 39(10):857-8. PubMed ID: 22594859
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Identification of two novel mutations in Chinese patients with Dyschromatosis symmetrica hereditaria.
    Li M; Li C; Hua H; Zhu W; Lu Y; Yang L
    Arch Dermatol Res; 2005 Nov; 297(5):196-200. PubMed ID: 16215765
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria.
    Kono M; Akiyama M; Kondo T; Suzuki T; Suganuma M; Wataya-Kaneda M; Lam J; Shibaki A; Tomita Y
    J Dermatol; 2012 Sep; 39(9):819-21. PubMed ID: 23336285
    [No Abstract]   [Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family.
    Bukhari IA; El-Harith EA; Stuhrmann M
    J Eur Acad Dermatol Venereol; 2006 May; 20(5):628-9. PubMed ID: 16684309
    [No Abstract]   [Full Text] [Related]  

  • 30. A new mutation of the double-stranded RNA-specific adenosine deaminase gene in a family with dyschromatosis symmetrica hereditaria.
    Liu Y; Xiao S; Peng Z; Chu Y; Wang J; Li X; Zhou S
    Dermatology; 2006; 213(3):200-3. PubMed ID: 17033168
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation.
    Nuber UA; Tinschert S; Mundlos S; Hauber I
    Am J Med Genet A; 2004 Mar; 125A(3):261-6. PubMed ID: 14994234
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dyschromatosis universalis hereditaria.
    Sethuraman G; Srinivas CR; D'Souza M; Thappa DM; Smiles L
    Clin Exp Dermatol; 2002 Sep; 27(6):477-9. PubMed ID: 12372090
    [TBL] [Abstract][Full Text] [Related]  

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

  • 36. Dyschromatosis symmetrica hereditaria with neurological abnormalities.
    Dutta A; Ghosh SK; Mandal RK
    Indian J Dermatol Venereol Leprol; 2014; 80(6):549-51. PubMed ID: 25382520
    [No Abstract]   [Full Text] [Related]  

  • 37. Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation.
    Tojo K; Sekijima Y; Suzuki T; Suzuki N; Tomita Y; Yoshida K; Hashimoto T; Ikeda S
    Mov Disord; 2006 Sep; 21(9):1510-3. PubMed ID: 16817193
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Patient with dyschromatosis symmetrica hereditaria treated with miniature punch grafting, followed by excimer light therapy.
    Kawakami T; Otaguchi R; Kyoya M; Soma Y; Suzuki T
    J Dermatol; 2013 Sep; 40(9):771-2. PubMed ID: 23803141
    [No Abstract]   [Full Text] [Related]  

  • 39. Genetical studies on skin diseases. I. Ephelides, dyschromatosis symmetrica hereditaria and xeroderma pigmentosum.
    ITO M
    Tohoku J Exp Med; 1950 Dec; 53(1/2):69-76. PubMed ID: 14828625
    [No Abstract]   [Full Text] [Related]  

  • 40. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China.
    He PP; He CD; Cui Y; Yang S; Xu HH; Li M; Yuan WT; Gao M; Liang YH; Li CR; Xu SJ; Chen JJ; Chen HD; Huang W; Zhang XJ
    Br J Dermatol; 2004 Apr; 150(4):633-9. PubMed ID: 15099357
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.