Halle D - Search Results

1

High frequency of BRCA1 and BRCA2 germline mutations in Ashkenazi Jewish ovarian cancer patients, regardless of family history.

Beller U, Halle D, Catane R, Kaufman B, Hornreich G, Levy-Lahad E. Beller U, et al. Among authors: halle d. Gynecol Oncol. 1997 Nov;67(2):123-6. doi: 10.1006/gyno.1997.4844. Gynecol Oncol. 1997. PMID: 9367693

2

Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families.

Levy-Lahad E, Catane R, Eisenberg S, Kaufman B, Hornreich G, Lishinsky E, Shohat M, Weber BL, Beller U, Lahad A, Halle D. Levy-Lahad E, et al. Among authors: halle d. Am J Hum Genet. 1997 May;60(5):1059-67. Am J Hum Genet. 1997. PMID: 9150153 Free PMC article.

3

Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes.

Friedman E, Bar-Sade Bruchim R, Kruglikova A, Risel S, Levy-Lahad E, Halle D, Bar-On E, Gershoni-Baruch R, Dagan E, Kepten I, Peretz T, Lerer I, Wienberg N, Shushan A, Abeliovich AD. Friedman E, et al. Among authors: halle d. Am J Hum Genet. 1998 Oct;63(4):1224-7. doi: 10.1086/302040. Am J Hum Genet. 1998. PMID: 9758598 Free PMC article. No abstract available.

4

A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families.

Yakobson E, Eisenberg S, Isacson R, Halle D, Levy-Lahad E, Catane R, Safro M, Sobolev V, Huot T, Peters G, Ruiz A, Malvehy J, Puig S, Chompret A, Avril MF, Shafir R, Peretz H, Bressac-de Paillerets B. Yakobson E, et al. Among authors: halle d. Eur J Hum Genet. 2003 Apr;11(4):288-96. doi: 10.1038/sj.ejhg.5200961. Eur J Hum Genet. 2003. PMID: 12700603

5

High prevalence of complement C7 deficiency among healthy blood donors of Moroccan Jewish ancestry.

Halle D, Elstein D, Geudalia D, Sasson A, Shinar E, Schlesinger M, Zimran A. Halle D, et al. Am J Med Genet. 2001 Apr 1;99(4):325-7. doi: 10.1002/ajmg.1183. Am J Med Genet. 2001. PMID: 11252001

6

Primary hyperoxaluria type I: a model for multiple mutations in a monogenic disease within a distinct ethnic group.

Rinat C, Wanders RJ, Drukker A, Halle D, Frishberg Y. Rinat C, et al. Among authors: halle d. J Am Soc Nephrol. 1999 Nov;10(11):2352-8. doi: 10.1681/ASN.V10112352. J Am Soc Nephrol. 1999. PMID: 10541294

7

Genetic polymorphisms of the renin-angiotensin system and the outcome of focal segmental glomerulosclerosis in children.

Frishberg Y, Becker-Cohen R, Halle D, Feigin E, Eisenstein B, Halevy R, Lotan D, Juabeh I, Ish-Shalom N, Magen D, Shvil Y, Sinai-Treiman L, Drukker A. Frishberg Y, et al. Among authors: halle d. Kidney Int. 1998 Dec;54(6):1843-9. doi: 10.1046/j.1523-1755.1998.00218.x. Kidney Int. 1998. PMID: 9853248 Free article.

8

[Androgen receptor and male infertility].

Eldar-Geva T, Milatiner D, Halle D. Eldar-Geva T, et al. Among authors: halle d. Harefuah. 2004 Jun;143(6):432-9, 461. Harefuah. 2004. PMID: 15524101 Review. Hebrew.

9

Genetic polymorphism in paraoxonase is a risk factor for childhood focal segmental glomerulosclerosis.

Frishberg Y, Toledano H, Becker-Cohen R, Feigin E, Halle D. Frishberg Y, et al. Among authors: halle d. Am J Kidney Dis. 2000 Dec;36(6):1253-61. doi: 10.1053/ajkd.2000.19842. Am J Kidney Dis. 2000. PMID: 11096050

10

C7 complement deficiency in an Israeli Arab village.

Behar D, Schlesinger M, Halle D, Ben-Ami H, Edoute Y, Shahar E, Kasis I, Shihab S, Elstein D, Zimran A, Mandel H. Behar D, et al. Among authors: halle d. Am J Med Genet. 2002 Jun 1;110(1):25-9. doi: 10.1002/ajmg.10393. Am J Med Genet. 2002. PMID: 12116267

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

47 results

Search Page

Filters