BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

330 related articles for article (PubMed ID: 28407215)

  • 1. Updated review of genetic reticulate pigmentary disorders.
    Zhang J; Li M; Yao Z
    Br J Dermatol; 2017 Oct; 177(4):945-959. PubMed ID: 28407215
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inherited Reticulate Pigmentary Disorders.
    Lin MH; Chou PC; Lee IC; Yang SF; Yu HS; Yu S
    Genes (Basel); 2023 Jun; 14(6):. PubMed ID: 37372478
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dyschromatosis symmetrica hereditaria and reticulate acropigmentation of Kitamura: An update.
    Kono M; Akiyama M
    J Dermatol Sci; 2019 Feb; 93(2):75-81. PubMed ID: 30692041
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The spectrum of reticulate pigment disorders of the skin revisited.
    Müller CS; Tremezaygues L; Pföhler C; Vogt T
    Eur J Dermatol; 2012; 22(5):596-604. PubMed ID: 23018017
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Follicular Dowling Degos disease: a rare variant of an evolving dermatosis.
    Singh S; Khandpur S; Verma P; Singh M
    Indian J Dermatol Venereol Leprol; 2013; 79(6):802-4. PubMed ID: 24177614
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dowling-Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura.
    Kono M; Suganuma M; Takama H; Zarzoso I; Saritha M; Bodet D; Aboobacker S; Kaliaperumal K; Suzuki T; Tomita Y; Sugiura K; Akiyama M
    Br J Dermatol; 2015 Aug; 173(2):584-6. PubMed ID: 25639155
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Reticulate hyperpigmentation.
    Schnur RE; Heymann WR
    Semin Cutan Med Surg; 1997 Mar; 16(1):72-80. PubMed ID: 9125768
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Reticulate acropigmentation of Kitamura with a novel mutation in ADAM10.
    Pan Y; Zhong W; Wang H; Yang Y; Lin Z
    Clin Exp Dermatol; 2019 Aug; 44(6):700-703. PubMed ID: 30488468
    [No Abstract]   [Full Text] [Related]  

  • 11. Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura.
    Buket Basmanav F; Fritz G; Lestringant GG; Pachat D; Hoffjan S; Fischer J; Wehner M; Wolf S; Thiele H; Altmüller J; Pulimood SA; Rütten A; Kruse R; Hanneken S; Frank J; Danda S; Bygum A; Betz RC
    J Invest Dermatol; 2015 Feb; 135(2):615-618. PubMed ID: 25229252
    [No Abstract]   [Full Text] [Related]  

  • 12. Genome-wide linkage and exome sequencing analyses identify an initiation codon mutation of KRT5 in a unique Chinese family with generalized Dowling-Degos disease.
    Li M; Wang J; Zhang J; Ni C; Li X; Liang J; Cheng R; Li Z; Yao Z
    Br J Dermatol; 2016 Mar; 174(3):663-6. PubMed ID: 26440693
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Dyschromatosis Universalis Hereditaria with Oral Leukokeratosis--A Case of Mistaken Identity and Review of the Literature.
    Sorensen RH; Werner KA; Kobayashi TT
    Pediatr Dermatol; 2015; 32(6):e283-7. PubMed ID: 26269252
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Retyping and molecular pathology diagnosis of dyschromatosis universalis hereditaria.
    Zhou D; Yang P; Chen H
    Exp Dermatol; 2023 Sep; 32(9):1334-1343. PubMed ID: 37353900
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders.
    Alshaikh H; Alsaif F; Aldukhi S
    Dermatol Res Pract; 2017; 2017():3518568. PubMed ID: 29201043
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical Overlaps in Reticulate Pigmentary Disorders: A Study of Three Cases.
    Malik N; Nair RS; Reddy A; Chaurasia P; Pillai NS
    Cureus; 2024 Mar; 16(3):e56600. PubMed ID: 38646262
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Successful treatment of Dowling-Degos disease using intense pulsed light.
    Gupta A; Huilgol SC
    Australas J Dermatol; 2015 Aug; 56(3):e63-5. PubMed ID: 25495801
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.
    Kono M; Sugiura K; Suganuma M; Hayashi M; Takama H; Suzuki T; Matsunaga K; Tomita Y; Akiyama M
    Hum Mol Genet; 2013 Sep; 22(17):3524-33. PubMed ID: 23666529
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dowling-Degos disease associated with hidradenitis suppurativa: a case report.
    Arjona-Aguilera C; Linares-Barrios M; Albarrán-Planelles C; Jiménez-Gallo D
    Actas Dermosifiliogr; 2015 May; 106(4):337-8. PubMed ID: 25529465
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 17.