Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Michal Feingold"'
Autor:
Lena Sagi-Dain, Idit Maya, Michal Feingold-Zadok, Shay Ben Shachar, Amihood Singer, Anat Bar-Shira, Tzipora C. Falik-Zaccai, Amir Peleg
Publikováno v:
Archives of Gynecology and Obstetrics. 304:649-656
To analyze the risk for clinically significant microarray aberrations in pregnancies with polyhydramnios. Data from all chromosomal microarray analyses (CMA) performed due to polyhydramnios between January 2013 and December 2019 were retrospectively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4847ed6aedbcb48619b0f14200452381
https://doi.org/10.1007/s00404-021-05995-y
https://doi.org/10.1007/s00404-021-05995-y
Autor:
Amihood Singer, Morad Khayat, Rachel Michaelson-Cohen, Hagit Daum, Lena Sagi-Dain, Keren Tzadikevitch Geffen, Shay Ben-Shachar, Rivka Sukenik Halevy, Michal Feingold-Zadok, Idit Maya
Publikováno v:
Archives of Gynecology and Obstetrics. 303:85-92
To investigate the prevalence of pathogenic and likely-pathogenic variants detected by chromosomal microarray analysis (CMA), among pregnancies with fetal short long bones diagnosed by ultrasound. The study cohort was based on cases of chromosomal mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a3c0131402b0b5926ab940d26230949
https://doi.org/10.1007/s00404-020-05729-6
https://doi.org/10.1007/s00404-020-05729-6
Autor:
Morad Khayat, Yael Pasternak, Rivka Sukenik Halevy, Sharon Zeligson, Shay Ben-Shachar, Amihood Singer, Lena Sagi-Dain, Michal Feingold-Zadok, Lior Greenbaum, Idit Maya
Publikováno v:
Journal of Perinatal Medicine. 48:553-558
Objectives Chromosomal microarray analysis (CMA) is the method of choice for genetic work-up in cases of fetal malformations. We assessed the detection rate of CMA in cases of abnormal fetal head circumference (HC). Methods The study cohort was based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e628d1d8437bfb3b57e9b8602f0baab
https://doi.org/10.1515/jpm-2020-0048
https://doi.org/10.1515/jpm-2020-0048
Autor:
Michal Feingold-Zadok, Lior Greenbaum, Shay Ben Shachar, Sagi Josefsberg Ben Yehoshua, Amihood Singer, Lena Sagi-Dain, Idit Maya
Publikováno v:
Obstetrics and gynecology. 137(1)
Objective To examine the risk of clinically significant chromosomal microarray analysis findings in fetuses with nuchal translucency from 3.0-3.4 mm. In addition, we aimed to define the yield of noninvasive prenatal testing (NIPT) in such pregnancies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::136e13cdd249596d9f9c06531847d2b6
https://pubmed.ncbi.nlm.nih.gov/33278279
https://pubmed.ncbi.nlm.nih.gov/33278279
Autor:
Lena, Sagi-Dain, Amihood, Singer, Tzipora, Falik-Zaccai, Amir, Peleg, Anat, Bar-Shira, Michal, Feingold-Zadok, Shay, Ben Shachar, Idit, Maya
Publikováno v:
Archives of gynecology and obstetrics. 304(3)
To analyze the risk for clinically significant microarray aberrations in pregnancies with polyhydramnios.Data from all chromosomal microarray analyses (CMA) performed due to polyhydramnios between January 2013 and December 2019 were retrospectively o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::784a88693cef9a76d3a639d4d079665f
https://pubmed.ncbi.nlm.nih.gov/33591382
https://pubmed.ncbi.nlm.nih.gov/33591382
Autor:
Lena Sagi-Dain, Rachel Michaelson-Cohen, Rivka Sukenik Halevy, Amihood Singer, Hagit Daum, Keren Tzadikevitch Geffen, Shay Ben-Shachar, Michal Feingold-Zadok, Lior Greenbaum, Idit Maya
Publikováno v:
Fetal diagnosis and therapy. 48(2)
Introduction: We evaluated the yield of chromosomal microarray analysis in pregnancies complicated with fetal growth restriction (FGR) according to specific clinical parameters. Methods: The study was based on national records from the Israeli Minist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3fba02f1e9fe74b682b5a6d9b8b6317
https://pubmed.ncbi.nlm.nih.gov/33352557
https://pubmed.ncbi.nlm.nih.gov/33352557
Autor:
Keren, Tzadikevitch Geffen, Amihood, Singer, Idit, Maya, Lena, Sagi-Dain, Morad, Khayat, Shay, Ben-Shachar, Hagit, Daum, Rachel, Michaelson-Cohen, Michal, Feingold-Zadok, Rivka, Sukenik Halevy
Publikováno v:
Archives of gynecology and obstetrics. 303(1)
To investigate the prevalence of pathogenic and likely-pathogenic variants detected by chromosomal microarray analysis (CMA), among pregnancies with fetal short long bones diagnosed by ultrasound.The study cohort was based on cases of chromosomal mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e79f749030c2ad921120b4beaf87481
https://pubmed.ncbi.nlm.nih.gov/32761367
https://pubmed.ncbi.nlm.nih.gov/32761367
Publikováno v:
Genetics in Medicine. 24:S302
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fed9957c1f05539508191d7323540687
https://doi.org/10.1016/j.gim.2022.01.608
https://doi.org/10.1016/j.gim.2022.01.608
Autor:
Amihood Singer, Ehud Kaliner, Dorit Lev, Ayala Frumkin, Lena Sagi-Dain, Tzipora C. Falik-Zaccai, Shay Ben Shachar, Hagit Yonath, Michal Feingold-Zadok, Idit Maya
Publikováno v:
European journal of obstetrics, gynecology, and reproductive biology. 222
Objective To examine the risk for clinically significant chromosomal microarray analysis (CMA) among fetuses with apparently isolated horseshoe kidney. Methods Data from all CMA analyses performed due to isolated horseshoe kidney reported to the Isra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1165bb47a6613f62f560716af7c33b88
https://pubmed.ncbi.nlm.nih.gov/29367169
https://pubmed.ncbi.nlm.nih.gov/29367169
Autor:
Michal, Feingold-Zadok, David, Chitayat, Karen, Chong, Marie, Injeyan, Patrick, Shannon, Daphne, Chapmann, Ron, Maymon, Nir, Pillar, Orit, Reish
Publikováno v:
Prenatal diagnosis. 37(2)
We studied a series of patients with fetal akinesia deformation sequence (FADS)/arthrogryposis multiplex congenita (AMC), with nemaline bodies on muscle specimens, which revealed mutations in the NEB gene.We pathologically assessed seven cases from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ecd2b1ed319f78d9e46dc3646d1499ff
https://pubmed.ncbi.nlm.nih.gov/27933661
https://pubmed.ncbi.nlm.nih.gov/27933661