BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 9114612)

  • 1. Dyschromatosis universalis hereditaria: an electron microscopic examination.
    Kim NS; Im S; Kim SC
    J Dermatol; 1997 Mar; 24(3):161-4. PubMed ID: 9114612
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Ultrastructural Investigations in an Autosomal Recessively Inherited Case of Dyschromatosis Universalis Hereditaria.
    Gupta A; Sharma Y; Dash KN; Verma S; Natarajan VT; Singh A
    Acta Derm Venereol; 2015 Jul; 95(6):738-40. PubMed ID: 25474346
    [No Abstract]   [Full Text] [Related]  

  • 4. Hereditary congenital hypopigmented and hyperpigmented macules.
    Westerhof W; Beemer FA; Cormane RH; Delleman JW; Faber WR; de Jong JG; van der Schaar WW
    Arch Dermatol; 1978 Jun; 114(6):931-6. PubMed ID: 666331
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Dyschromatosis universalis hereditaria in a young Nigerian female.
    Yusuf SM; Mijinyawa MS; Maiyaki MB; Mohammed AZ
    Int J Dermatol; 2009 Jul; 48(7):749-50. PubMed ID: 19570083
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Behavior of melanocytes in reticulate acropigmentation of Kitamura.
    Mizoguchi M; Kukita A
    Arch Dermatol; 1985 May; 121(5):659-61. PubMed ID: 3994414
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Three-dimensional structure analysis of melanocytes and keratinocytes in senile lentigo.
    Mizutani Y; Yamashita M; Hashimoto R; Atsugi T; Ryu A; Hayashi A; Rikimaru-Nishi Y; Ohta K
    Microscopy (Oxf); 2021 Mar; 70(2):224-231. PubMed ID: 32991711
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dyschromatosis universalis hereditaria: report of a case.
    Kao CH; Yu HS; Ko SS
    J Formos Med Assoc; 1991 Dec; 90(12):1205-10. PubMed ID: 1686890
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria.
    Liu JW; Habulieti X; Wang RR; Ma DL; Zhang X
    J Clin Lab Anal; 2021 Jun; 35(6):e23803. PubMed ID: 34028087
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Dyschromatosis universalis hereditaria: a rare entity.
    Kumar S; Mahajan BB; Singh R
    Dermatol Online J; 2011 Jul; 17(7):6. PubMed ID: 21810391
    [TBL] [Abstract][Full Text] [Related]  

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

  • 18. 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]  

  • 19. Mutations in ABCB6 cause dyschromatosis universalis hereditaria.
    Zhang C; Li D; Zhang J; Chen X; Huang M; Archacki S; Tian Y; Ren W; Mei A; Zhang Q; Fang M; Su Z; Yin Y; Liu D; Chen Y; Cui X; Li C; Yang H; Wang Q; Wang J; Liu M; Deng Y
    J Invest Dermatol; 2013 Sep; 133(9):2221-8. PubMed ID: 23519333
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.
    Liu H; Li Y; Hung KK; Wang N; Wang C; Chen X; Sheng D; Fu X; See K; Foo JN; Low H; Liany H; Irwan ID; Liu J; Yang B; Chen M; Yu Y; Yu G; Niu G; You J; Zhou Y; Ma S; Wang T; Yan X; Goh BK; Common JE; Lane BE; Sun Y; Zhou G; Lu X; Wang Z; Tian H; Cao Y; Chen S; Liu Q; Liu J; Zhang F
    PLoS One; 2014; 9(2):e87250. PubMed ID: 24498303
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.