Search Results - "Mey-Raz N"

Preimplantation genetic diagnosis for Duchenne muscular dystrophy

Authors: Malcov, M. Mey-Raz, N. Carmon, A. et al.

Source: Fertility & Sterility. Oct2004 Supplement 1, Vol. 82, pS245-S246. 0p.

Timing embryo biopsy for PGD – before or after cryopreservation?

Authors: Shinar, S. Kornecki, N. Schwartz, T. et al.

Source: Gynecological Endocrinology. Sep2016, Vol. 32 Issue 9, p756-758. 3p.

Preimplantation genetic diagnosis for fragile X syndrome in Israel

Authors: Malcov, M. Carmon, A. Mey-Raz, N. et al.

Source: Fertility & Sterility. Oct2004 Supplement 1, Vol. 82, pS246-S247. 0p.

Interval double transfer improves treatment success in patients with repeated IVF/ET failures.

Authors: Almog, B. Levin, I. Wagman, I. et al.

Source: Journal of Assisted Reproduction & Genetics. Aug2008, Vol. 25 Issue 8, p353-357. 5p. 2 Charts.

Spindle imaging: a new marker for optimal timing of ICSI?

Authors: Cohen, Y. Malcov, M. Schwartz, T. et al.

Source: Human Reproduction. Vol. 19 Issue 3, p649-654. 6p. 1 Diagram, 4 Charts.

Time-lapse microscopic analysis to verify how blastomere biopsy for PGD affects the dynamics of embryonic development.

Authors: Ben-Yosef, D. Bar-El, L. Shwartz, T. et al.

Source: Fertility & Sterility. Sep2014, Vol. 102 Issue S, pe19-e20. 1p.

P-279: Interval double transfer improves treatment success in patients with repeated IVF/ET failures

Authors: Almog, B. Levin, I. Wagman, I. et al.

Source: Fertility & Sterility. Sep2006 Supplement, Vol. 86, pS238-S239. 0p.

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

Authors: Malcov M Naiman T Yosef DB et al.

Source: Reproductive biomedicine online [Reprod Biomed Online] 2007 Apr; Vol. 14 (4), pp. 515-21.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101122473 Publication Model: Print Cited Medium: Print ISSN: 1472-6483 (Print) Linking ISSN: 14726483 NLM ISO Abbreviation: Reprod Biomed Online Subsets: MEDLINE

Preimplantation genetic diagnosis of Canavan disease.

Authors: Yaron Y Schwartz T Mey-Raz N et al.

Source: Fetal diagnosis and therapy [Fetal Diagn Ther] 2005 Sep-Oct; Vol. 20 (5), pp. 465-8.

Publication Type: Journal Article

Journal Info: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 9107463 Publication Model: Print Cited Medium: Print ISSN: 1015-3837 (Print) Linking ISSN: 10153837 NLM ISO Abbreviation: Fetal Diagn Ther Subsets: MEDLINE

An association between embryo morphology and high concentrations of plasma anticardiolipin antibodies.

Authors: Schwartz, T. Mey-Raz, N. Geva, E. et al.

Source: Human reproduction 1998; Vol. 13 (suppl_4).

Journal Info: Publisher: Oxford University Press / USA ISSN: 0268-1161

Female sex bias in human embryonic stem cell lines.

Authors: Ben-Yosef D Amit A Malcov M et al.

Source: Stem cells and development [Stem Cells Dev] 2012 Feb 10; Vol. 21 (3), pp. 363-72. Date of Electronic Publication: 2011 Jun 24.

Publication Type: Comparative Study; Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101197107 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-8534 (Electronic) Linking ISSN: 15473287 NLM ISO Abbreviation: Stem Cells Dev Subsets: MEDLINE

Retrieval of immature oocytes after chemotherapy for Hodgkin's disease and prolonged ovarian down-regulation with gonadotropin-releasing hormone agonist.

Authors: Azem F Hasson J Cohen T et al.

Source: Fertility and sterility [Fertil Steril] 2009 Aug; Vol. 92 (2), pp. 828.e1-2. Date of Electronic Publication: 2009 Jun 13.

Publication Type: Comparative Study; Controlled Clinical Trial; Journal Article

Journal Info: Publisher: Elsevier for the American Society for Reproductive Medicine Country of Publication: United States NLM ID: 0372772 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1556-5653 (Electronic) Linking ISSN: 00150282 NLM ISO Abbreviation: Fertil Steril Subsets: MEDLINE

Detection of spinal muscular atrophy carriers by nested polymerase chain reaction of single sperm cells.

Authors: Yaron Y Cohen T Mey-Raz N et al.

Source: Genetic testing [Genet Test] 2006 Spring; Vol. 10 (1), pp. 18-23.

Publication Type: Journal Article

Journal Info: Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 9802546 Publication Model: Print Cited Medium: Print ISSN: 1090-6576 (Print) Linking ISSN: 10906576 NLM ISO Abbreviation: Genet Test Subsets: MEDLINE

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

Authors: Malcov M Ben-Yosef D Schwartz T et al.

Source: Prenatal diagnosis [Prenat Diagn] 2005 Dec; Vol. 25 (13), pp. 1200-5.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print Cited Medium: Print ISSN: 0197-3851 (Print) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE