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 *

115 related articles for article (PubMed ID: 3809028)

  • 1. A case of xeroderma pigmentosum with clinical appearance of dyschromatosis symmetrica hereditaria.
    Nishigori C; Miyachi Y; Takebe H; Imamura S
    Pediatr Dermatol; 1986 Nov; 3(5):410-3. PubMed ID: 3809028
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Useful applications of DNA repair tests for differential diagnosis of atypical dyschromatosis symmetrica hereditaria from xeroderma pigmentosum.
    Ohtoshi E; Matsumura Y; Nishigori C; Toda KI; Horiguchi Y; Ikenaga M; Miyachi Y
    Br J Dermatol; 2001 Jan; 144(1):162-8. PubMed ID: 11167700
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report.
    Patrizi A; Manneschi V; Pini A; Baioni E; Ghetti P
    Acta Derm Venereol; 1994 Mar; 74(2):135-7. PubMed ID: 7911621
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dyschromatosis.
    Urabe K; Hori Y
    Semin Cutan Med Surg; 1997 Mar; 16(1):81-5. PubMed ID: 9125769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Localized form of dyschromatosis universalis hereditaria in a 14-year-old girl.
    Dhar S; Malakar S
    Pediatr Dermatol; 1999; 16(4):336. PubMed ID: 10515773
    [No Abstract]   [Full Text] [Related]  

  • 6. Sunlight is merely a temporary modifier of dyschromatosis symmetrica hereditaria.
    Kono M; Miyamura Y; Tomita Y; Akiyama M
    Eur J Dermatol; 2018 Apr; 28(2):251-252. PubMed ID: 29400290
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. [Xeroderma pigmentosum and pigmented xerodermoid. Clinical and molecular biological studies].
    Jung EG; Schnyder UW
    Schweiz Med Wochenschr; 1970 Oct; 100(41):1718-26. PubMed ID: 5480540
    [No Abstract]   [Full Text] [Related]  

  • 9. Clinical and photobiological differences between dyschromatosis symmetrica hereditaria and xeroderma pigmentosum.
    Satoh Y; Yoshida M
    J Dermatol; 1980 Oct; 7(5):317-22. PubMed ID: 7009681
    [No Abstract]   [Full Text] [Related]  

  • 10. Hyper- and hypopigmented macules over palms and soles since birth--a case of dyschromatosis symmetrica hereditaria.
    Hemmati I; Lam J
    Dermatol Online J; 2009 Nov; 15(11):5. PubMed ID: 19951641
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Xeroderma pigmentosum variant heterozygotes show reduced levels of recovery of replicative DNA synthesis in the presence of caffeine after ultraviolet irradiation.
    Itoh T; Linn S; Kamide R; Tokushige H; Katori N; Hosaka Y; Yamaizumi M
    J Invest Dermatol; 2000 Dec; 115(6):981-5. PubMed ID: 11121129
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Universal dyschromatosis: a familial case].
    Schoenlaub P; Leroy JP; Dupré D; Chaboche C; Plantin P
    Ann Dermatol Venereol; 1998 Oct; 125(10):700-4. PubMed ID: 9835959
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A simple method for diagnosing xeroderma pigmentosum variant.
    Itoh T; Ono T; Yamaizumi M
    J Invest Dermatol; 1996 Sep; 107(3):349-53. PubMed ID: 8751969
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reticulate acropigmentation of dohi: a case report with insight into genodermatoses with mottled pigmentation.
    Mohana D; Verma U; Amar AJ; Choudhary RK
    Indian J Dermatol; 2012 Jan; 57(1):42-4. PubMed ID: 22470208
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [A case of idiopathic brain calcification associated with dyschromatosis symmetrica hereditaria, aplasia of dental root, and aortic valve sclerosis].
    Tojyo K; Hattori T; Sekijima Y; Yoshida K; Ikeda S
    Rinsho Shinkeigaku; 2001 Jun; 41(6):299-305. PubMed ID: 11771159
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and photobiological characteristics of xeroderma pigmentosum complementation group F: a review of cases from Japan.
    Yamamura K; Ichihashi M; Hiramoto T; Ogoshi M; Nishioka K; Fujiwara Y
    Br J Dermatol; 1989 Oct; 121(4):471-80. PubMed ID: 2696553
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of melanoma in xeroderma pigmentosum.
    Rao TN; Bhagyalaxmi A; Ahmed K; Mohana Rao TS; Venkatachalam K
    Indian J Pathol Microbiol; 2009; 52(4):524-6. PubMed ID: 19805962
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Group D xeroderma pigmentosum: a case with a number of nevocellular nevi.
    Inoue Y; Yamaizumi M; Ono T
    J Dermatol; 1995 May; 22(5):360-4. PubMed ID: 7673558
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.