Peretz T - Search Results

1

Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.

Baris HN, Barnes-Kedar I, Toledano H, Halpern M, Hershkovitz D, Lossos A, Lerer I, Peretz T, Kariv R, Cohen S, Half EE, Magal N, Drasinover V, Wimmer K, Goldberg Y, Bercovich D, Levi Z. Baris HN, et al. Among authors: peretz t. Pediatr Blood Cancer. 2016 Mar;63(3):418-27. doi: 10.1002/pbc.25818. Epub 2015 Nov 6. Pediatr Blood Cancer. 2016. PMID: 26544533

2

The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women.

Abeliovich D, Kaduri L, Lerer I, Weinberg N, Amir G, Sagi M, Zlotogora J, Heching N, Peretz T. Abeliovich D, et al. Among authors: peretz t. Am J Hum Genet. 1997 Mar;60(3):505-14. Am J Hum Genet. 1997. PMID: 9042909 Free PMC article.

3

Cisplatin-induced non-convulsive encephalopathy.

Lyass O, Lossos A, Hubert A, Gips M, Peretz T. Lyass O, et al. Among authors: peretz t. Anticancer Drugs. 1998 Jan;9(1):100-4. doi: 10.1097/00001813-199801000-00013. Anticancer Drugs. 1998. PMID: 9491799

4

Genetic testing of breast and ovarian cancer patients: clinical characteristics and hormonal risk modifiers.

Kaduri L, Gibs M, Hubert A, Sagi M, Heching N, Lerer I, Uziely B, Weinberg N, Abeliovich D, Peretz T. Kaduri L, et al. Among authors: peretz t. Eur J Obstet Gynecol Reprod Biol. 1999 Jul;85(1):75-80. doi: 10.1016/s0301-2115(98)00286-3. Eur J Obstet Gynecol Reprod Biol. 1999. PMID: 10428326

5

[Brief preoperative radiotherapy reduces local recurrences and improves survival in rectal cancer].

Peretz T, Weshler Z, Goldberg Y, Durst AL, Freund HR. Peretz T, et al. Harefuah. 2000 Jan 16;138(2):96-9, 175. Harefuah. 2000. PMID: 10883067 Hebrew.

6

A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: a possible role of the Alu-polyA tail in the evolution of the deletion.

Wang T, Lerer I, Gueta Z, Sagi M, Kadouri L, Peretz T, Abeliovich D. Wang T, et al. Among authors: peretz t. Genes Chromosomes Cancer. 2001 May;31(1):91-5. doi: 10.1002/gcc.1110. Genes Chromosomes Cancer. 2001. PMID: 11284040

7

A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi Jews.

Rennert H, Bercovich D, Hubert A, Abeliovich D, Rozovsky U, Bar-Shira A, Soloviov S, Schreiber L, Matzkin H, Rennert G, Kadouri L, Peretz T, Yaron Y, Orr-Urtreger A. Rennert H, et al. Among authors: peretz t. Am J Hum Genet. 2002 Oct;71(4):981-4. doi: 10.1086/342775. Epub 2002 Jul 23. Am J Hum Genet. 2002. PMID: 12145743 Free PMC article.

8

A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer.

Kadouri L, Bercovich D, Elimelech A, Lerer I, Sagi M, Glusman G, Shochat C, Korem S, Hamburger T, Nissan A, Abu-Halaf N, Badrriyah M, Abeliovich D, Peretz T. Kadouri L, et al. Among authors: peretz t. BMC Cancer. 2007 Jan 18;7:14. doi: 10.1186/1471-2407-7-14. BMC Cancer. 2007. PMID: 17233897 Free PMC article.

9

Mutation spectrum in HNPCC in the Israeli population.

Goldberg Y, Porat RM, Kedar I, Shochat C, Sagi M, Eilat A, Mendelson S, Hamburger T, Nissan A, Hubert A, Kadouri L, Pikarski E, Lerer I, Abeliovich D, Bercovich D, Peretz T. Goldberg Y, et al. Among authors: peretz t. Fam Cancer. 2008;7(4):309-17. doi: 10.1007/s10689-008-9191-y. Epub 2008 Apr 4. Fam Cancer. 2008. PMID: 18389388

10

Vincristine-induced paralytic ileus in Parkinson's disease.

Leker RR, Peretz T, Hubert A, Lossos A. Leker RR, et al. Among authors: peretz t. Parkinsonism Relat Disord. 1997 Apr;3(2):109-10. doi: 10.1016/s1353-8020(97)00008-4. Parkinsonism Relat Disord. 1997. PMID: 18591064

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