Amit A - Search Results

1

Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?

Reches A, Malcov M, Ben-Yosef D, Azem F, Amit A, Yaron Y. Reches A, et al. Among authors: amit a. Prenat Diagn. 2009 Jan;29(1):57-61. doi: 10.1002/pd.2179. Prenat Diagn. 2009. PMID: 19097038

2

Multiplex nested PCR for preimplantation genetic diagnosis of spinal muscular atrophy.

Malcov M, Schwartz T, Mei-Raz N, Yosef DB, Amit A, Lessing JB, Shomrat R, Orr-Urtreger A, Yaron Y. Malcov M, et al. Among authors: amit a. Fetal Diagn Ther. 2004 Mar-Apr;19(2):199-206. doi: 10.1159/000075151. Fetal Diagn Ther. 2004. PMID: 14764971

3

Preimplantation genetic diagnosis of Canavan disease.

Yaron Y, Schwartz T, Mey-Raz N, Amit A, Lessing JB, Malcov M. Yaron Y, et al. Among authors: amit a. Fetal Diagn Ther. 2005 Sep-Oct;20(5):465-8. doi: 10.1159/000086834. Fetal Diagn Ther. 2005. PMID: 16113575

4

Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.

Malcov M, Ben-Yosef D, Schwartz T, Mey-Raz N, Azem F, Lessing JB, Amit A, Yaron Y. Malcov M, et al. Among authors: amit a. Prenat Diagn. 2005 Dec;25(13):1200-5. doi: 10.1002/pd.1317. Prenat Diagn. 2005. PMID: 16353285

5

Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCR.

Malcov M, Naiman T, Yosef DB, Carmon A, Mey-Raz N, Amit A, Vagman I, Yaron Y. Malcov M, et al. Among authors: amit a. Reprod Biomed Online. 2007 Apr;14(4):515-21. doi: 10.1016/s1472-6483(10)60901-7. Reprod Biomed Online. 2007. PMID: 17425837

6

Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos.

Eiges R, Urbach A, Malcov M, Frumkin T, Schwartz T, Amit A, Yaron Y, Eden A, Yanuka O, Benvenisty N, Ben-Yosef D. Eiges R, et al. Among authors: amit a. Cell Stem Cell. 2007 Nov;1(5):568-77. doi: 10.1016/j.stem.2007.09.001. Cell Stem Cell. 2007. PMID: 18371394 Free article.

7

The effect of CGG repeat number on ovarian response among fragile X premutation carriers undergoing preimplantation genetic diagnosis.

Bibi G, Malcov M, Yuval Y, Reches A, Ben-Yosef D, Almog B, Amit A, Azem F. Bibi G, et al. Among authors: amit a. Fertil Steril. 2010 Aug;94(3):869-74. doi: 10.1016/j.fertnstert.2009.04.047. Epub 2009 May 29. Fertil Steril. 2010. PMID: 19481741 Free article.

8

Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia.

Malcov M, Reches A, Ben-Yosef D, Cohen T, Amit A, Dgany O, Tamary H, Yaron Y. Malcov M, et al. Among authors: amit a. Prenat Diagn. 2010 Mar;30(3):207-11. doi: 10.1002/pd.2437. Prenat Diagn. 2010. PMID: 20049848

9

[Preimplantation genetic diagnosis (PGD) for cancer predisposition syndromes].

Malcov M, Ben-Yosef D, Amit A, Yaron Y. Malcov M, et al. Among authors: amit a. Harefuah. 2011 Jun;150(6):496-501, 553. Harefuah. 2011. PMID: 21800485 Hebrew.

10

Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype.

Malcov M, Gold V, Peleg S, Frumkin T, Azem F, Amit A, Ben-Yosef D, Yaron Y, Reches A, Barda S, Kleiman SE, Yogev L, Hauser R. Malcov M, et al. Among authors: amit a. Reprod Biol Endocrinol. 2017 Apr 26;15(1):31. doi: 10.1186/s12958-017-0247-4. Reprod Biol Endocrinol. 2017. PMID: 28446182 Free PMC article.

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