Lin Z - Search Results

1

Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratoderma.

Liu J, Chen Z, Hu L, Song Z, Mo R, Tsang LS, Liu Y, Huang X, Gong Z, Xiang R, Lin Z, Yang Y. Liu J, et al. Among authors: lin z. Br J Dermatol. 2022 Dec;187(6):1043-1045. doi: 10.1111/bjd.21835. Epub 2022 Sep 7. Br J Dermatol. 2022. PMID: 35976164 No abstract available.

2

Dispersion of atrial repolarization in patients with paroxysmal atrial fibrillation.

Li Z, Hertervig E, Yuan S, Yang Y, Lin Z, Olsson SB. Li Z, et al. Among authors: lin z. Europace. 2001 Oct;3(4):285-91. doi: 10.1053/eupc.2001.0183. Europace. 2001. PMID: 11678386

3

A case of primary erythermalgia with prurigo.

Li Y, Lin Z, Ma Z, Yang Y. Li Y, et al. Among authors: lin z. Clin Exp Dermatol. 2009 Oct;34(7):e313-4. doi: 10.1111/j.1365-2230.2009.03265.x. Epub 2009 May 18. Clin Exp Dermatol. 2009. PMID: 19456783 No abstract available.

4

New mutations in the transglutaminase 1 gene in three families with lamellar ichthyosis.

Cao X, Lin Z, Yang H, Bu D, Tu P, Chen L, Wu H, Yang Y. Cao X, et al. Among authors: lin z. Clin Exp Dermatol. 2009 Dec;34(8):904-9. doi: 10.1111/j.1365-2230.2009.03288.x. Epub 2009 May 22. Clin Exp Dermatol. 2009. PMID: 19486042

5

A case of Hailey-Hailey disease in an infant with a new ATP2C1 gene mutation.

Xu Z, Zhang L, Xiao Y, Li L, Lin Z, Yang Y, Ma L. Xu Z, et al. Among authors: lin z. Pediatr Dermatol. 2011 Mar-Apr;28(2):165-8. doi: 10.1111/j.1525-1470.2010.01088.x. Pediatr Dermatol. 2011. PMID: 20403116

6

Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia.

Lin Z, Chen Q, Shi L, Lee M, Giehl KA, Tang Z, Wang H, Zhang J, Yin J, Wu L, Xiao R, Liu X, Dai L, Zhu X, Li R, Betz RC, Zhang X, Yang Y. Lin Z, et al. Am J Hum Genet. 2012 Nov 2;91(5):906-11. doi: 10.1016/j.ajhg.2012.08.029. Epub 2012 Oct 11. Am J Hum Genet. 2012. PMID: 23063621 Free PMC article.

7

Mutation in AQP5, encoding aquaporin 5, causes palmoplantar keratoderma Bothnia type.

Cao X, Yin J, Wang H, Zhao J, Zhang J, Dai L, Zhang J, Jiang H, Lin Z, Yang Y. Cao X, et al. Among authors: lin z. J Invest Dermatol. 2014 Jan;134(1):284-287. doi: 10.1038/jid.2013.302. Epub 2013 Jul 18. J Invest Dermatol. 2014. PMID: 23867895 Free article. No abstract available.

8

New and recurrent SERPINB7 mutations in seven Chinese patients with Nagashima-type palmoplantar keratosis.

Yin J, Xu G, Wang H, Zhao J, Duo L, Cao X, Tang Z, Lin Z, Yang Y. Yin J, et al. Among authors: lin z. J Invest Dermatol. 2014 Aug;134(8):2269-2272. doi: 10.1038/jid.2014.80. Epub 2014 Feb 10. J Invest Dermatol. 2014. PMID: 24514002 Free article. No abstract available.

9

ITGB4-associated junctional epidermolysis bullosa without pylori atresia but profound genito-urinary involvement.

Lee M, Chen Q, Wang H, Zhang J, Lin Z, Yang Y. Lee M, et al. Among authors: lin z. Acta Derm Venereol. 2015 Jan;95(1):112-3. doi: 10.2340/00015555-1888. Acta Derm Venereol. 2015. PMID: 24807042 Free article. No abstract available.

10

Compound heterozygous PLEC mutations in a patient of consanguineous parentage with epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia.

Yin J, Ren Y, Lin Z, Wang H, Zhou Y, Yang Y. Yin J, et al. Among authors: lin z. Int J Dermatol. 2015 Feb;54(2):185-7. doi: 10.1111/ijd.12655. Epub 2014 Sep 10. Int J Dermatol. 2015. PMID: 25209331

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