Abeliovich D - Search Results

1

Genetics of cerebrotendinous xanthomatosis (CTX): an autosomal recessive trait with high gene frequency in Sephardim of Moroccan origin.

Berginer VM, Abeliovich D. Berginer VM, et al. Among authors: abeliovich d. Am J Med Genet. 1981;10(2):151-7. doi: 10.1002/ajmg.1320100209. Am J Med Genet. 1981. PMID: 7315872

2

Klinefelter's and Takayasu's syndromes in one patient--a pure coincidence?

Berginer VM, Paran E, Hirsch M, Abeliovich D. Berginer VM, et al. Among authors: abeliovich d. Angiology. 1983 Mar;34(3):170-5. doi: 10.1177/000331978303400302. Angiology. 1983. PMID: 6131629

3

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: abeliovich d. 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.

4

Genetic screening in patients with Retinoblastoma in Israel.

Sagi M, Frenkel A, Eilat A, Weinberg N, Frenkel S, Pe'er J, Abeliovich D, Lerer I. Sagi M, et al. Among authors: abeliovich d. Fam Cancer. 2015 Sep;14(3):471-80. doi: 10.1007/s10689-015-9794-z. Fam Cancer. 2015. PMID: 25754945

5

Lynch Syndrome in high risk Ashkenazi Jews in Israel.

Goldberg Y, Kedar I, Kariiv R, Halpern N, Plesser M, Hubert A, Kaduri L, Sagi M, Lerer I, Abeliovich D, Hamburger T, Nissan A, Goldshmidt H, Solar I, Geva R, Strul H, Rosner G, Baris H, Levi Z, Peretz T. Goldberg Y, et al. Among authors: abeliovich d. Fam Cancer. 2014 Mar;13(1):65-73. doi: 10.1007/s10689-013-9675-2. Fam Cancer. 2014. PMID: 23990280

6

Carrier frequency of two BBS2 mutations in the Ashkenazi population.

Fedick A, Jalas C, Abeliovich D, Krakinovsky Y, Ekstein J, Ekstein A, Treff NR. Fedick A, et al. Among authors: abeliovich d. Clin Genet. 2014 Jun;85(6):578-82. doi: 10.1111/cge.12231. Epub 2013 Jul 28. Clin Genet. 2014. PMID: 23829372

7

Complex chromosomal rearrangement in a girl with psychomotor-retardation and a de novo inversion: inv(2)(p15;q24.2).

Granot-Hershkovitz E, Raas-Rothschild A, Frumkin A, Granot D, Silverstein S, Abeliovich D. Granot-Hershkovitz E, et al. Among authors: abeliovich d. Am J Med Genet A. 2011 Aug;155A(8):1825-32. doi: 10.1002/ajmg.a.33952. Epub 2011 Jul 7. Am J Med Genet A. 2011. PMID: 21739571

8

ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia.

Glaser B, Blech I, Krakinovsky Y, Ekstein J, Gillis D, Mazor-Aronovitch K, Landau H, Abeliovich D. Glaser B, et al. Among authors: abeliovich d. Genet Med. 2011 Oct;13(10):891-4. doi: 10.1097/GIM.0b013e31821fea33. Genet Med. 2011. PMID: 21716120 Free article.

9

Interstitial insertion of RARα gene into PML gene in a patient with acute promyelocytic leukemia (APL) lacking the classic t(15;17).

Goldschmidt N, Yehuda-Gafni O, Abeliovich D, Slyusarevsky E, Rund D. Goldschmidt N, et al. Among authors: abeliovich d. Hematology. 2010 Oct;15(5):332-7. doi: 10.1179/102453310X12647083621083. Hematology. 2010. PMID: 20863428

10

An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC.

Goldberg Y, Porat RM, Kedar I, Shochat C, Galinsky D, Hamburger T, Hubert A, Strul H, Kariiv R, Ben-Avi L, Savion M, Pikarsky E, Abeliovich D, Bercovich D, Lerer I, Peretz T. Goldberg Y, et al. Among authors: abeliovich d. Fam Cancer. 2010 Jun;9(2):141-50. doi: 10.1007/s10689-009-9298-9. Fam Cancer. 2010. PMID: 19851887

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