Li CR - Search Results

1

[Alpha-galactosidase A gene mutation in a Chinese family with Fabry disease mimicking clinical features of hypertrophic cardiomyopathy].

Liu HJ, Cao KJ, Li CR, Dai J, Ma JZ, Yong YH, Sun W. Liu HJ, et al. Among authors: li cr. Zhonghua Xin Xue Guan Bing Za Zhi. 2006 Feb;34(2):143-7. Zhonghua Xin Xue Guan Bing Za Zhi. 2006. PMID: 16626582 Chinese.

2

A new arginine substitution mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.

Li CR, Li M, Ma HJ, Luo D, Yang LJ, Wang DG, Zhu XH, Yue XZ, Chen WQ, Zhu WY. Li CR, et al. Among authors: li m. J Dermatol Sci. 2005 Feb;37(2):95-9. doi: 10.1016/j.jdermsci.2004.11.004. Epub 2004 Dec 21. J Dermatol Sci. 2005. PMID: 15659327

3

One novel homozygous mutation of SLC39A4 gene in a Chinese patient with acrodermatitis enteropathica.

Li CR, Yan SM, Shen DB, Li Q, Shao JP, Xue CY, Cao YH. Li CR, et al. Among authors: li q. Arch Dermatol Res. 2010 May;302(4):315-7. doi: 10.1007/s00403-010-1047-2. Epub 2010 Mar 19. Arch Dermatol Res. 2010. PMID: 20300938

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. Li CR, et al. Among authors: li m. Arch Dermatol Res. 2010 Aug;302(6):477-80. doi: 10.1007/s00403-010-1037-4. Epub 2010 Mar 19. Arch Dermatol Res. 2010. PMID: 20300939

5

Identification of a novel mutation in a Chinese patient with mild Darier's disease.

Li CR, Cui PG, Jia H, Wang HS, Chen M, Zhou WQ, Gong JQ, Cao YH, Lin L. Li CR, et al. Int J Dermatol. 2010 Nov;49(11):1286-8. doi: 10.1111/j.1365-4632.2009.04159.x. Int J Dermatol. 2010. PMID: 20964649 No abstract available.

6

A novel missense mutation of the ATP2C1 gene in a Chinese patient with papular acantholytic dermatosis of the anogenital area.

Xiao X, Chen L, Wang B, Li C. Xiao X, et al. Indian J Dermatol Venereol Leprol. 2016 Jul-Aug;82(4):429-31. doi: 10.4103/0378-6323.181206. Indian J Dermatol Venereol Leprol. 2016. PMID: 27279308 Free article. No abstract available.

7

A gene locus responsible for reticulate pigmented anomaly of the flexures maps to chromosome 17p13.3.

Li CR, Xing QH, Li M, Qin W, Yue XZ, Zhang XJ, Ma HJ, Wang DG, Feng GY, Zhu WY, He L. Li CR, et al. Among authors: li m. J Invest Dermatol. 2006 Jun;126(6):1297-301. doi: 10.1038/sj.jid.5700271. J Invest Dermatol. 2006. PMID: 16575392 Free article.

8

A novel missense mutation in ADAR1 gene causing dyschromatosis symmetrica hereditaria in a Chinese patient.

Li ZL, Zhang GY, Hui Y, Yu RX, Li Q, Xu HX, Li CR. Li ZL, et al. Among authors: li cr, li q. Indian J Dermatol Venereol Leprol. 2015 May-Jun;81(3):327. doi: 10.4103/0378-6323.155560. Indian J Dermatol Venereol Leprol. 2015. PMID: 25900931 Free article. No abstract available.

9

A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling.

Jia WX, Xiao XM, Wu JB, Ma YP, Ge YP, Li Q, Mao QX, Li CR. Jia WX, et al. Among authors: li cr, li q. Ther Clin Risk Manag. 2015 Apr 21;11:635-8. doi: 10.2147/TCRM.S75544. eCollection 2015. Ther Clin Risk Manag. 2015. PMID: 25960657 Free PMC article.

10

Mal de Meleda with homozygous mutation p.G86R in SLURP-1.

Jia WX, Zhang YY, Wu YD, Li WR, Cheng P, Bu WB, Li CR. Jia WX, et al. Among authors: li cr, li wr. Int J Dermatol. 2020 Jun;59(6):751-754. doi: 10.1111/ijd.14807. Epub 2020 Feb 12. Int J Dermatol. 2020. PMID: 32048728 No abstract available.

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