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Michal Feingold

Showing results (1-10 of 15) with videos related to

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Fertility and Sterility|November 8, 2008
The clinical characteristics and sonographic findings of maternal ovarian torsion in pregnancyNoam Smorgick, Moty Pansky, Michal Feingold, et al.
JSLS : Journal of the Society of Laparoendoscopic Surgeons|August 3, 2006
Diagnostic hysteroscopy as a primary tool in a basic infertility workupMoty Pansky, Michal Feingold, Ron Sagi, et al.
Molecular Genetics and Metabolism|April 13, 2016
Terminal microdeletions of 13q34 chromosome region in patients with intellectual disability: Delineation of an emerging new microdeletion syndromeEyal Reinstein, Meytal Liberman, Michal Feingold-Zadok, et al.
Journal of Minimally Invasive Gynecology|October 20, 2009
Maternal adnexal torsion in pregnancy is associated with significant risk of recurrenceMoty Pansky, Michal Feingold, Ron Maymon, et al.
American Journal of Obstetrics and Gynecology|May 6, 2008
Can we rely on blind endometrial biopsy for detection of focal intrauterine pathology?Ran Svirsky, Noam Smorgick, Uri Rozowski, et al.
Obstetrics and Gynecology|December 5, 2020
Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mmLena Sagi-Dain, Amihood Singer, Shay Ben Shachar, et al.
Prenatal Diagnosis|December 10, 2016
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenitaMichal Feingold-Zadok, David Chitayat, Karen Chong, et al.
The Israel Medical Association Journal : IMAJ|October 17, 2023
Pregnancy with Facial Cleft: 20 Years of Experience at a Single CenterMarina Pekar-Zlotin, Natali Zilberman Sharon, Yaakov Melcer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 19, 2014
Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22Rony Cohen, Lina Basel-Vanagaite, Hadassah Goldberg-Stern, et al.
Archives of Gynecology and Obstetrics|February 16, 2021
The effect of polyhydramnios degree on chromosomal microarray results: a retrospective cohort analysis of 742 singleton pregnanciesLena Sagi-Dain, Amihood Singer, Tzipora Falik-Zaccai, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Fertility and Sterility|November 8, 2008
The clinical characteristics and sonographic findings of maternal ovarian torsion in pregnancyNoam Smorgick, Moty Pansky, Michal Feingold, et al.
JSLS : Journal of the Society of Laparoendoscopic Surgeons|August 3, 2006
Diagnostic hysteroscopy as a primary tool in a basic infertility workupMoty Pansky, Michal Feingold, Ron Sagi, et al.
Molecular Genetics and Metabolism|April 13, 2016
Terminal microdeletions of 13q34 chromosome region in patients with intellectual disability: Delineation of an emerging new microdeletion syndromeEyal Reinstein, Meytal Liberman, Michal Feingold-Zadok, et al.
Journal of Minimally Invasive Gynecology|October 20, 2009
Maternal adnexal torsion in pregnancy is associated with significant risk of recurrenceMoty Pansky, Michal Feingold, Ron Maymon, et al.
American Journal of Obstetrics and Gynecology|May 6, 2008
Can we rely on blind endometrial biopsy for detection of focal intrauterine pathology?Ran Svirsky, Noam Smorgick, Uri Rozowski, et al.
Obstetrics and Gynecology|December 5, 2020
Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mmLena Sagi-Dain, Amihood Singer, Shay Ben Shachar, et al.
Prenatal Diagnosis|December 10, 2016
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenitaMichal Feingold-Zadok, David Chitayat, Karen Chong, et al.
The Israel Medical Association Journal : IMAJ|October 17, 2023
Pregnancy with Facial Cleft: 20 Years of Experience at a Single CenterMarina Pekar-Zlotin, Natali Zilberman Sharon, Yaakov Melcer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 19, 2014
Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22Rony Cohen, Lina Basel-Vanagaite, Hadassah Goldberg-Stern, et al.
Archives of Gynecology and Obstetrics|February 16, 2021
The effect of polyhydramnios degree on chromosomal microarray results: a retrospective cohort analysis of 742 singleton pregnanciesLena Sagi-Dain, Amihood Singer, Tzipora Falik-Zaccai, et al.
Pageof 2