Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Shai E Elizur"'
Autor:
Shai E Elizur, Oshrit Lebovitz, Sanaz Derech-Haim, Olga Dratviman-Storobinsky, Baruch Feldman, Jehoshua Dor, Raoul Orvieto, Yoram Cohen
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e105121 (2014)
AimTo assess the role of mRNA accumulation in granulosa cells as the cause of low ovarian response among FMR1 premutation carriers undergoing pre-implantation genetic diagnosis (PGD).DesignCase control study in an academic IVF unit. Twenty-one consec
Externí odkaz:
https://doaj.org/article/e99f8137474546bb9b17c9b491fa3399
Autor:
Maya Shats, Yossi Bart, Yechiel Z. Burke, Shlomo B. Cohen, Mati Zolti, Michal Zajicek, Roy Mashiach, Elad Berkowitz, Shai E. Elizur
Publikováno v:
Fertility and Sterility. 119:1008-1015
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86febac24a8ac90e4654d283eaa9d315
https://doi.org/10.1016/j.fertnstert.2023.02.004
https://doi.org/10.1016/j.fertnstert.2023.02.004
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 107:3000-3009
Context FMR1 premutation (PM) carriers are at increased risk of ovarian impairment resulting in diminished ovarian response (DOR) to exogenous follicle-stimulating hormone (FSH) stimulation. Expanded CGG repeat transcript and RAN-associated protein (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c0e5d7d7606c471ae2bd93449b0c412
https://doi.org/10.1210/clinem/dgac536
https://doi.org/10.1210/clinem/dgac536
Autor:
Noam Domniz, Liat Ries-Levavi, Yoram Cohen, Lilach Marom-Haham, Michal Berkenstadt, Elon Pras, Anne Glicksman, Nicole Tortora, Gary J. Latham, Andrew G. Hadd, Sarah L. Nolin, Shai E. Elizur
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Introduction: Fragile X syndrome (FXS) is a common form of X-linked intellectual and developmental disability with a prevalence of 1/4000–5000 in males and 1/6000–8000 in females. Most cases of the syndrome result from expansion of a premutation
Externí odkaz:
https://doaj.org/article/85f39036183544a09bd54f90a3ea85fe
Autor:
Dorothy A. Fink, Lawrence M. Nelson, Reed Pyeritz, Josh Johnson, Stephanie L. Sherman, Yoram Cohen, Shai E. Elizur
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Abnormalities in the X-linked FMR1 gene are associated with a constellation of disorders, which have broad and profound implications for the person first diagnosed, and extended family members of all ages. The rare and pleiotropic nature of the assoc
Externí odkaz:
https://doaj.org/article/d7b1227cdcb842fea1d39eb7b5f600a7
Publikováno v:
Turkish journal of obstetrics and gynecology. 19(3)
This study aimed to examine the associations between follicular distribution pattern (FDP) in polycystic ovaries and menstrual disturbances in women with infertility.A retrospective review of patients was performed (n=73). Ultrasound images from cycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1f36056f8b2fb3406c39b3bb1962db0
https://pubmed.ncbi.nlm.nih.gov/36149262
https://pubmed.ncbi.nlm.nih.gov/36149262
Autor:
Shai E. Elizur, Adva Aizer, Michal Yonish, Tal Shavit, Raoul Orvieto, Roy Mashiach, Shlomo B. Cohen, Elad Berkowitz
Publikováno v:
Reproductive biomedicine online.
What is the outcome of fertility-preservation treatments in women with endometrioma, especially those with endometrioma larger than 4 cm?Retrospective cohort study. Women with definitive diagnosis of ovarian endometriosis (by histology or ultrasound)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b17dcc6f60ec85e95d6f76a6c77c376a
https://pubmed.ncbi.nlm.nih.gov/36564221
https://pubmed.ncbi.nlm.nih.gov/36564221
Publikováno v:
SN Comprehensive Clinical Medicine. 3:2127-2133
Endometriosis is a gynaecological disease in which cell tissue that lines inside of the uterine cavity (the endometrium) flourishes outside of the uterus. This leads to inflammation in the surrounding tissue and causes the main symptoms of endometrio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d2739a77284360d10fa7eaa6e434697
https://doi.org/10.1007/s42399-021-00983-4
https://doi.org/10.1007/s42399-021-00983-4
Autor:
Shai E. Elizur, Noam Domniz, Yoram Cohen, Shay Ben-Shachar, Liat Ries Levavi, Hila Raanani, Michal Berkenstadt, Elon Pras, Yuval Yaron, Dana Brabbing Goldstein
Publikováno v:
Genetics in Medicine. 23:1023-1027
PURPOSE To evaluate whether ethnicity affects the risk of full mutation expansion among females heterozygous for FMR1 premutation. METHODS Women who carry the FMR1 premutation alelle of Jewish origin who underwent fragile X prenatal diagnosis between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d087fb8cf4a7c3c95c6a9654733230a
https://doi.org/10.1038/s41436-020-01089-3
https://doi.org/10.1038/s41436-020-01089-3
Autor:
Noam Domniz, R. Orvieto, Hila Raanani, Moran Friedman-Gohas, Yoram Cohen, Shai E. Elizur, Michal Kirshenbaum, A Michaeli
Publikováno v:
J Assist Reprod Genet
PURPOSE: While FMR1 premutation carriers (CGG 55–200) were shown to have reduced success with IVF treatment (lower oocyte yield), studies reporting on the association between the number of CGG repeats and patients’ response to controlled ovarian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d752bdafa5f903fa74f6014cc03a063a
https://doi.org/10.1007/s10815-020-01701-0
https://doi.org/10.1007/s10815-020-01701-0