438 related articles for article (PubMed ID: 19951641)
1. 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]
2. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases.
Oyama M; Shimizu H; Ohata Y; Tajima S; Nishikawa T
Br J Dermatol; 1999 Mar; 140(3):491-6. PubMed ID: 10233273
[TBL] [Abstract][Full Text] [Related]
3. A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.
Li M; Jiang YX; Liu JB; Yang S; He PP; Gao M; Wei SC; Yan KL; Huang W; Zhang XJ
Clin Exp Dermatol; 2004 Sep; 29(5):533-5. PubMed ID: 15347341
[TBL] [Abstract][Full Text] [Related]
4. Two new mutations of the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.
Li CR; Xu XL; Sun XJ; Zong WK; Sheng N; Bu J; Li M; Cui PG
Arch Dermatol Res; 2010 Aug; 302(6):477-80. PubMed ID: 20300939
[TBL] [Abstract][Full Text] [Related]
5. Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria.
Binitha MP; Thomas D; Asha LK
Indian J Dermatol Venereol Leprol; 2006; 72(4):300-2. PubMed ID: 16880579
[TBL] [Abstract][Full Text] [Related]
6. Dyschromatosis.
Urabe K; Hori Y
Semin Cutan Med Surg; 1997 Mar; 16(1):81-5. PubMed ID: 9125769
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. Five novel mutations of RNA-specific adenosine deaminase gene with dyschromatosis symmetrica hereditaria.
Hou Y; Chen J; Gao M; Zhou F; Du W; Shen Y; Yang S; Zhang XJ
Acta Derm Venereol; 2007; 87(1):18-21. PubMed ID: 17225010
[TBL] [Abstract][Full Text] [Related]
15. A novel insertion mutation in the ADAR1 gene of a Chinese family with dyschromatosis symmetrica hereditaria.
Zhu CY; Zhu KJ; Zhou Y; Fan YM
Genet Mol Res; 2013 Aug; 12(3):2858-62. PubMed ID: 24065641
[TBL] [Abstract][Full Text] [Related]
16. Dyschromatosis universalis hereditaria.
Murthy AB; Palaniappan V; Karthikeyan K; Anbarasan V
Int J Dermatol; 2023 Oct; 62(10):1218-1227. PubMed ID: 37634201
[TBL] [Abstract][Full Text] [Related]
17. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21.
Zhang XJ; Gao M; Li M; Li M; Li CR; Cui Y; He PP; Xu SJ; Xiong XY; Wang ZX; Yuan WT; Yang S; Huang W
J Invest Dermatol; 2003 May; 120(5):776-80. PubMed ID: 12713580
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
