Peretz H - Search Results

1

Role of CYP2D6 polymorphism in predicting liver fibrosis progression rate in Caucasian patients with chronic hepatitis C.

Fishman S, Lurie Y, Peretz H, Morad T, Grynberg E, Blendis LM, Leshno M, Brazowski E, Rosner G, Halpern Z, Oren R. Fishman S, et al. Among authors: peretz h. Liver Int. 2006 Apr;26(3):279-84. doi: 10.1111/j.1478-3231.2005.01236.x. Liver Int. 2006. PMID: 16584388

2

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.

3

Apolipoprotein-E genotype and the risk of developing cholelithiasis following bariatric surgery: a clue to prevention of routine prophylactic cholecystectomy.

Abu Abeid S, Szold A, Gavert N, Goldiner I, Grynberg E, Peretz H, Konikoff FM. Abu Abeid S, et al. Among authors: peretz h. Obes Surg. 2002 Jun;12(3):354-7. doi: 10.1381/096089202321087850. Obes Surg. 2002. PMID: 12087994

4

Cys 618 Arg mutation in the RET proto-oncogene associated with familial medullary thyroid carcinoma and maternally transmitted Hirschsprung's disease suggesting a role for imprinting.

Peretz H, Luboshitsky R, Baron E, Biton A, Gershoni R, Usher S, Grynberg E, Yakobson E, Graff E, Lapidot M. Peretz H, et al. Hum Mutat. 1997;10(2):155-9. doi: 10.1002/(SICI)1098-1004(1997)10:2<155::AID-HUMU7>3.0.CO;2-J. Hum Mutat. 1997. PMID: 9259198

5

Cytokine network in nonresponding chronic hepatitis C patients with genotype 1: role of triple therapy with interferon alpha, ribavirin, and ursodeoxycholate.

Neuman MG, Blendis LM, Shear NH, Malkiewicz IM, Ibrahim A, Katz GG, Sapir D, Halpern Z, Brill S, Peretz H, Magazinik S, Konikoff FM. Neuman MG, et al. Among authors: peretz h. Clin Biochem. 2001 May;34(3):183-8. doi: 10.1016/s0009-9120(01)00213-2. Clin Biochem. 2001. PMID: 11408015 Clinical Trial.

6

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

7

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

8

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

9

Detection of the Glanzmann's thrombasthenia mutations in Arab and Iraqi-Jewish patients by polymerase chain reaction and restriction analysis of blood or urine samples.

Peretz H, Seligsohn U, Zwang E, Coller BS, Newman PJ. Peretz H, et al. Thromb Haemost. 1991 Oct 1;66(4):500-4. Thromb Haemost. 1991. PMID: 1796402

10

A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene.

Zivelin A, Rosenberg N, Faier S, Kornbrot N, Peretz H, Mannhalter C, Horellou MH, Seligsohn U. Zivelin A, et al. Among authors: peretz h. Blood. 1998 Aug 15;92(4):1119-24. Blood. 1998. PMID: 9694698 Free article.

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