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 *

197 related articles for article (PubMed ID: 19584476)

  • 21. Dyschromatosis universalis hereditaria: a case report.
    Udayashankar C; Nath AK
    Dermatol Online J; 2011 Feb; 17(2):2. PubMed ID: 21382285
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical and genetic features of myoclonus-dystonia in 3 cases: a video presentation.
    Kock N; Kasten M; Schüle B; Hedrich K; Wiegers K; Kabakci K; Hagenah J; Pramstaller PP; Nitschke MF; Münchau A; Sperner J; Klein C
    Mov Disord; 2004 Feb; 19(2):231-4. PubMed ID: 14978685
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Dyschromatosis universalis hereditaria: a case report.
    Kumar S; Rajendra O; Prasad H
    Int J Dermatol; 2014 Mar; 53(3):342-5. PubMed ID: 24320734
    [No Abstract]   [Full Text] [Related]  

  • 24. 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]  

  • 25. Dyschromatosis universalis hereditaria: report of six cases from a family.
    Sardar SK; Das A; Bandyopadhyay DB
    Dermatol Online J; 2016 Sep; 22(9):. PubMed ID: 28329614
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dyschromatosis symmetrica hereditaria with acral hypertrophy.
    Murata T; Yagi Y; Tanioka M; Suzuki T; Miyachi Y; Morita K; Utani A
    Eur J Dermatol; 2011; 21(4):649-50. PubMed ID: 21840790
    [No Abstract]   [Full Text] [Related]  

  • 27. Dowling-Degos disease with diffuse penile pigmentation.
    Taskapan O; Gokce E; Akin O; Erkilinc AC; Demirkesen C
    J Eur Acad Dermatol Venereol; 2014 Oct; 28(10):1405-6. PubMed ID: 24422879
    [No Abstract]   [Full Text] [Related]  

  • 28. Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing.
    Liu JW; ; Sun J; Vano-Galvan S; Liu FX; Wei XX; Ma DL
    Chin Med J (Engl); 2016 Jan; 129(1):33-8. PubMed ID: 26712430
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Analysis on the mutation of ADAR gene in a pedigree with dyschromatosis symmetrical hereditaria].
    Li M; Yang LJ; Zhu XH; Zhang HP; Dai XY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):446-8. PubMed ID: 17680540
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Dyschromatosis symmetrica hereditaria in an Indian family.
    Hemanthkumar ; Thappa DM
    J Dermatol; 1999 Aug; 26(8):544-5. PubMed ID: 10487014
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. Dowling-Degos disease.
    Georgescu EF; Stănescu L; Popescu CF; Comănescu M; Georgescu I
    Rom J Morphol Embryol; 2010; 51(1):181-5. PubMed ID: 20191141
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A missense mutation c.G2747A (p.R916Q) of ADAR1 gene in dyschromatosis symmetrica hereditaria is not a novel mutation.
    Hayashi M; Suzuki T
    Arch Dermatol Res; 2010 Aug; 302(6):481-2. PubMed ID: 20169444
    [No Abstract]   [Full Text] [Related]  

  • 34. 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]  

  • 35. Novel mutations in
    Zhong WL; Wang HJ; Lin ZM; Yang Y
    Indian J Dermatol Venereol Leprol; 2019; 85(4):440. PubMed ID: 29956681
    [No Abstract]   [Full Text] [Related]  

  • 36. A novel missense mutation in DSRAD in a family with dyschromatosis symmetrica hereditaria.
    Li M; Yang LJ; Shi YX; Huang HY
    Arch Dermatol Res; 2007 Aug; 299(5-6):273-5. PubMed ID: 17569068
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel deletion mutation of the DSRAD gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria.
    Chao SC; Lee JY; Sheu HM; Yang MH
    Br J Dermatol; 2005 Nov; 153(5):1064-6. PubMed ID: 16225627
    [No Abstract]   [Full Text] [Related]  

  • 38. Dyschromatosis universalis hereditaria: two cases.
    Kenani N; Ghariani N; Denguezli M; Sriha B; Belajouza C; Nouira R
    Dermatol Online J; 2008 Feb; 14(2):16. PubMed ID: 18700119
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Dyschromatosis Universalis Hereditaria.
    Bista M; Agrawal S; Agrawal Y
    Kathmandu Univ Med J (KUMJ); 2021 Jan.-Mar; 19(73):146-147. PubMed ID: 34812175
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Hereditary dystonias].
    Hjermind LE; Sørensen SA; Werdelin LM
    Ugeskr Laeger; 2000 Sep; 162(38):5066-70. PubMed ID: 11014135
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.