Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Rosemary Reiss"'
Autor:
S. Jennifer Wang, Shivi Maheswaran, Rosemary Reiss, Leah H. Portnow, Jane Brock, Lara Novak, Jessica Erdmann-Sager, Thanh U. Barbie
Publikováno v:
Case Reports in Surgery, Vol 2023 (2023)
Introduction. Pseudoangiomatous stromal hyperplasia (PASH) presenting as gigantomastia is rare in pregnancy but can result in severe clinical consequences for both mother and fetus. Case Presentation. A 43-year-old female with a history of biopsy-pro
Externí odkaz:
https://doaj.org/article/6dfae661ec0a44d5ba9f93b6b885c2ab
Publikováno v:
Infectious Diseases in Obstetrics and Gynecology, Vol 1, Iss 1, Pp 46-48 (1993)
Maternal and neonatal infections with Salmonella typhi have been well documented. There are only two previous case reports of intrauterine infection with non-typhoidal species. This paper presents a third case of maternal septicemia followed by neona
Externí odkaz:
https://doaj.org/article/b61947e656e04bb999eb4de342a969f2
Publikováno v:
Prenatal Diagnosis. 37:515-520
Objectives To assess the incidence of sex chromosome aneuploidy (SCA) predicted by noninvasive prenatal testing (NIPT), assess test performance, and compare it with nuchal translucency (NT) screening among patients seen in our prenatal diagnosis cent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96ff4feda88941f47bbf6cb25d4cba6e
https://doi.org/10.1002/pd.5039
https://doi.org/10.1002/pd.5039
Publikováno v:
Obstetrical & Gynecological Survey. 72:583-585
Objectives To assess the incidence of sex chromosome aneuploidy (SCA) predicted by noninvasive prenatal testing (NIPT), assess test performance, and compare it with nuchal translucency (NT) screening among patients seen in our prenatal diagnosis cent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11b5707277afa39153097698cc6f18be
https://doi.org/10.1097/01.ogx.0000525895.44669.3e
https://doi.org/10.1097/01.ogx.0000525895.44669.3e
Publikováno v:
Prenatal diagnosis. 37(13)
Objective To review the literature for survival and phenotypes of liveborns with autosomal monosomy to inform decisions regarding transfer of in vitro fertilization-derived embryos reported as monosomic on preimplantation genetic testing for aneuploi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cec276870cdcbe7b58f62c6b5d3f208
https://pubmed.ncbi.nlm.nih.gov/29164644
https://pubmed.ncbi.nlm.nih.gov/29164644
Autor:
Sandra A. Farrell, Berivan Baskin, Kate Gardiner, Rosanna Weksberg, Cheryl Shuman, Shoshana J. Wodak, Deborah Terespolsky, Rosemary Reiss, Susan Blaser, Peter N. Ray, David Chitayat, Shuye Pu, Sanaa Choufani
Publikováno v:
American Journal of Medical Genetics Part A. :1388-1394
Beckwith-Wiedemann syndrome (BWS) is an overgrowth disorder with variability in clinical manifestations and molecular causes. In most cases, patients with BWS have normal development. Cases with developmental delay are usually attributed to neonatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21fedf689dc2209374a7817b7db6395b
https://doi.org/10.1002/ajmg.a.35358
https://doi.org/10.1002/ajmg.a.35358
Publikováno v:
Prenatal Diagnosis. 31:299-306
Objective To assess karyotypes and outcomes of monochorionic diamniotic (MCDA) twin pregnancies discordant for markedly enlarged nuchal translucency (NT) in the first trimester. Method Brigham and Women's Hospital's ultrasound database was queried to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd207fb7eefa791ea9513f17fe6a878e
https://doi.org/10.1002/pd.2691
https://doi.org/10.1002/pd.2691
Autor:
Fabiola Quintero-Rivera, Caroline D. Robson, John B. Mulliken, Carol B. Benson, Virginia Kimonis, Deborah Levine, Rosemary Reiss
Publikováno v:
Prenatal Diagnosis. 26:966-972
Apert syndrome was diagnosed in a newborn with typical facial and digital features whose only detected prenatal abnormality had been agenesis of the corpus callosum. This prompted a review of the central nervous system findings in all cases of Apert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6991499b4948a3bd0d2cdfe8b2a6ae3b
https://doi.org/10.1002/pd.1539
https://doi.org/10.1002/pd.1539
Publikováno v:
American journal of medical genetics. Part A. (3)
A 15q26 terminal chromosomal microdeletion was associated with markedly enlarged 1st trimester nuchal translucency in three of four pregnancies of a couple seen in our prenatal diagnosis unit. Nuchal translucency was normal in the couple's fourth pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed6ed9ad3999a36a92d8487843db1279
https://pubmed.ncbi.nlm.nih.gov/25691414
https://pubmed.ncbi.nlm.nih.gov/25691414
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine. 33(4)
Objectives The purpose of this study was to determine how often a low-lying placenta, defined as a placenta ending within 2 cm of the internal cervical os but not covering it, diagnosed sonographically in the second trimester resolves before delivery
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edbe7802d728bdecb04eb00db27ba4b9
https://pubmed.ncbi.nlm.nih.gov/24658950
https://pubmed.ncbi.nlm.nih.gov/24658950