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Items: 1 to 20 of 78

1.

Maternal-fetal vitamin D receptor polymorphisms significantly associated with preterm birth.

Rosenfeld T, Salem H, Altarescu G, Grisaru-Granovsky S, Tevet A, Birk R.

Arch Gynecol Obstet. 2017 Aug;296(2):215-222. doi: 10.1007/s00404-017-4412-y. Epub 2017 Jun 13.

PMID:
28612095
2.

Children with type 1 Gaucher disease: Changing profiles in the 21st century.

Elstein D, Altarescu G, Abrahamov A, Zimran A.

Blood Cells Mol Dis. 2016 Dec 19. pii: S1079-9796(16)30141-3. doi: 10.1016/j.bcmd.2016.12.009. [Epub ahead of print]

PMID:
28185830
3.

Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem Cells.

Cohen-Hadad Y, Altarescu G, Eldar-Geva T, Levi-Lahad E, Zhang M, Rogaeva E, Gotkine M, Bartok O, Ashwal-Fluss R, Kadener S, Epsztejn-Litman S, Eiges R.

Stem Cell Reports. 2016 Nov 8;7(5):927-940. doi: 10.1016/j.stemcr.2016.09.011. Epub 2016 Oct 20.

4.

Prevention is the Best Therapy: The Geneticist's Approach.

Altarescu G.

Pediatr Endocrinol Rev. 2016 Jun;13 Suppl 1:649-54.

PMID:
27491212
5.

Maternal and neonatal leptin and leptin receptor polymorphisms associated with preterm birth.

Salem H, Rosenfeld T, Altarescu G, Grisaru-Granovsky S, Birk R.

Gene. 2016 Oct 10;591(1):209-13. doi: 10.1016/j.gene.2016.07.014. Epub 2016 Jul 5.

PMID:
27393653
6.

Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis.

Epsztejn-Litman S, Cohen-Hadad Y, Aharoni S, Altarescu G, Renbaum P, Levy-Lahad E, Schonberger O, Eldar-Geva T, Zeligson S, Eiges R.

PLoS One. 2015 Oct 16;10(10):e0138893. doi: 10.1371/journal.pone.0138893. eCollection 2015.

7.

Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations.

Zeevi DA, Altarescu G, Weinberg-Shukron A, Zahdeh F, Dinur T, Chicco G, Herskovitz Y, Renbaum P, Elstein D, Levy-Lahad E, Rolfs A, Zimran A.

J Clin Invest. 2015 Oct 1;125(10):3757-65. doi: 10.1172/JCI79322. Epub 2015 Aug 31.

8.

Preimplantation genetic risk reduction: a new dilemma in the era of chromosomal microarrays and exome sequencing.

Altarescu G, Beeri R, Lazer-Derbeko G, Eldar-Geva T, Steinberg A, Levy-Lahad E, Renbaum P.

Reprod Biomed Online. 2015 Nov;31(5):706-10. doi: 10.1016/j.rbmo.2015.07.002. Epub 2015 Jul 17.

PMID:
26380867
9.

Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells.

Yanovsky-Dagan S, Avitzour M, Altarescu G, Renbaum P, Eldar-Geva T, Schonberger O, Mitrani-Rosenbaum S, Levy-Lahad E, Birnbaum RY, Gepstein L, Epsztejn-Litman S, Eiges R.

Stem Cell Reports. 2015 Aug 11;5(2):221-31. doi: 10.1016/j.stemcr.2015.06.003. Epub 2015 Jul 16.

10.

Developmental neuropsychological assessment of 4- to 5-year-old children born following Preimplantation Genetic Diagnosis (PGD): A pilot study.

Sacks GC, Altarescu G, Guedalia J, Varshaver I, Gilboa T, Levy-Lahad E, Eldar-Geva T.

Child Neuropsychol. 2016;22(4):458-71. doi: 10.1080/09297049.2015.1014900. Epub 2015 Mar 16.

PMID:
25774437
11.

Screening for Gaucher disease: new challenges.

Zimran A, Altarescu G, Elstein D.

Isr Med Assoc J. 2014 Nov;16(11):723-4. No abstract available.

12.

Protease-activated-receptor 1 polymorphisms correlate with risk for unexplained recurrent pregnancy loss: a pilot study querying an association beyond coagulation.

Grisaru-Granovsky S, Salah Z, Maoz M, Tevet A, Margalioth E, Samueloff A, Altarescu G, Bar-Shavit R.

Eur J Obstet Gynecol Reprod Biol. 2015 Feb;185:13-8. doi: 10.1016/j.ejogrb.2014.11.021. Epub 2014 Nov 25.

PMID:
25496845
13.

FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells.

Avitzour M, Mor-Shaked H, Yanovsky-Dagan S, Aharoni S, Altarescu G, Renbaum P, Eldar-Geva T, Schonberger O, Levy-Lahad E, Epsztejn-Litman S, Eiges R.

Stem Cell Reports. 2014 Nov 11;3(5):699-706. doi: 10.1016/j.stemcr.2014.09.001. Epub 2014 Oct 3.

14.

α-Synuclein rs356219 polymorphisms in patients with Gaucher disease and Parkinson disease.

Altarescu G, Ioscovich D, Alcalay RN, Zimran A, Elstein D.

Neurosci Lett. 2014 Sep 19;580:104-7. doi: 10.1016/j.neulet.2014.07.051. Epub 2014 Aug 8.

PMID:
25111979
15.

An intronic haplotype in α galactosidase A is associated with reduced mRNA expression in males with cryptogenic stroke.

Zeevi DA, Hakam-Spector E, Herskovitz Y, Beeri R, Elstein D, Altarescu G.

Gene. 2014 Oct 10;549(2):275-9. doi: 10.1016/j.gene.2014.08.004. Epub 2014 Aug 4.

PMID:
25101867
16.

Neonatal outcome after preimplantation genetic diagnosis.

Eldar-Geva T, Srebnik N, Altarescu G, Varshaver I, Brooks B, Levy-Lahad E, Bromiker R, Schimmel MS.

Fertil Steril. 2014 Oct;102(4):1016-21. doi: 10.1016/j.fertnstert.2014.06.023. Epub 2014 Jul 23.

PMID:
25064409
17.

Vitamin D receptor polymorphism FokI is associated with spontaneous idiopathic preterm birth in an Israeli population.

Manzon L, Altarescu G, Tevet A, Schimmel MS, Elstein D, Samueloff A, Grisaru-Granovsky S.

Eur J Obstet Gynecol Reprod Biol. 2014 Jun;177:84-8. doi: 10.1016/j.ejogrb.2014.03.008. Epub 2014 Mar 15.

PMID:
24702903
18.

Anesthetic management for oocyte retrieval: An exploratory analysis comparing outcome in in vitro fertilization cycles with and without pre-implantation genetic diagnosis.

Ioscovich A, Eldar-Geva T, Weitman M, Altarescu G, Rivilis A, Elstein D.

J Hum Reprod Sci. 2013 Oct;6(4):263-6. doi: 10.4103/0974-1208.126303.

19.

Achievement of therapeutic goals with low-dose imiglucerase in Gaucher disease: a single-center experience.

Tukan I, Hadas-Halpern I, Altarescu G, Abrahamov A, Elstein D, Zimran A.

Adv Hematol. 2013;2013:151506. doi: 10.1155/2013/151506. Epub 2013 Oct 28.

20.

Angiotensinogen promoter and angiotensinogen II receptor type 1 gene polymorphisms and incidence of ischemic stroke and neurologic phenotype in Fabry disease.

Altarescu G, Haim S, Elstein D.

Biomarkers. 2013 Nov;18(7):595-600. doi: 10.3109/1354750X.2013.836244. Epub 2013 Sep 10.

PMID:
24020479

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