Peretz H - Search Results

1

Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosis.

Ben Assayag E, Shenhar-Tsarfaty S, Bova I, Berliner S, Usher S, Peretz H, Shapira I, Bornstein NM. Ben Assayag E, et al. Among authors: peretz h. Thromb Res. 2009 Sep;124(4):458-62. doi: 10.1016/j.thromres.2009.04.008. Epub 2009 May 9. Thromb Res. 2009. PMID: 19428053

2

Gender differences in the expression of erythrocyte aggregation in relation to B beta-fibrinogen gene polymorphisms in apparently healthy individuals.

Ben Assayag E, Bova I, Berliner S, Peretz H, Usher S, Shapira I, Bornstein NM. Ben Assayag E, et al. Among authors: peretz h. Thromb Haemost. 2006 Mar;95(3):428-33. doi: 10.1160/TH05-08-0578. Thromb Haemost. 2006. PMID: 16525569

3

Triggered C-reactive protein (CRP) concentrations and the CRP gene -717A>G polymorphism in acute stroke or transient ischemic attack.

Ben-Assayag E, Shenhar-Tsarfaty S, Bova I, Berliner S, Shopin L, Peretz H, Usher S, Shapira I, Bornstein NM. Ben-Assayag E, et al. Among authors: peretz h. Eur J Neurol. 2007 Mar;14(3):315-20. doi: 10.1111/j.1468-1331.2006.01661.x. Eur J Neurol. 2007. PMID: 17355554

4

Glycohaemoglobin as a determinant of increased fibrinogen concentrations and low-grade inflammation in apparently healthy nondiabetic individuals.

Rogowski O, Shapira I, Peretz H, Berliner S. Rogowski O, et al. Among authors: peretz h. Clin Endocrinol (Oxf). 2008 Feb;68(2):182-9. doi: 10.1111/j.1365-2265.2007.03017.x. Epub 2007 Sep 4. Clin Endocrinol (Oxf). 2008. PMID: 17803696

5

Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews.

Peretz H, Salomon O, Mor-Cohen R, Usher S, Zucker M, Zivelin A, Seligsohn U. Peretz H, et al. J Thromb Haemost. 2013 Apr;11(4):724-30. doi: 10.1111/jth.12137. J Thromb Haemost. 2013. PMID: 23332144 Free article.

6

Increased fibrosis progression rates in hepatitis C patients carrying the prothrombin G20210A mutation.

Maharshak N, Halfon P, Deutsch V, Peretz H, Berliner S, Fishman S, Zelber-Sagi S, Rozovski U, Leshno M, Oren R. Maharshak N, et al. Among authors: peretz h. World J Gastroenterol. 2011 Dec 7;17(45):5007-13. doi: 10.3748/wjg.v17.i45.5007. World J Gastroenterol. 2011. PMID: 22174551 Free PMC article.

7

Current strategy for genetic analysis of haemophilia A families.

Dardik R, Peretz H, Usher S, Seligsohn U, Martinowitz U. Dardik R, et al. Among authors: peretz h. Haemophilia. 1996 Jan;2(1):11-7. doi: 10.1111/j.1365-2516.1996.tb00003.x. Haemophilia. 1996. PMID: 27213899

8

Screening for tumour suppressor p16(CDKN2A) germline mutations in Israeli melanoma families.

Yakobson EA, Zlotogorski A, Shafir R, Cohen M, Icekson M, Landau M, Brenner S, Usher S, Peretz H. Yakobson EA, et al. Among authors: peretz h. Clin Chem Lab Med. 1998 Aug;36(8):645-8. doi: 10.1515/CCLM.1998.114. Clin Chem Lab Med. 1998. PMID: 9806478

9

Enzyme analysis of amniotic fluid for prenatal diagnosis of cystic fibrosis in high-risk pregnancies.

Peretz H, Chemke J, Usher S, Legum C, Graff E. Peretz H, et al. Clin Chem. 1988 Dec;34(12):2401-5. Clin Chem. 1988. PMID: 2904307

10

An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming belt.

Peretz H, Korostishevsky M, Steinberg DM, Kabha M, Usher S, Krause I, Shalev H, Landau D, Levartovsky D. Peretz H, et al. JIMD Rep. 2019 Dec 5;51(1):45-52. doi: 10.1002/jmd2.12077. eCollection 2020 Jan. JIMD Rep. 2019. PMID: 32071838 Free PMC article.

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