Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rodney A. McLaren, Jr"'
Publikováno v:
AJOG Global Reports, Vol 4, Iss 3, Pp 100356- (2024)
BACKGROUND: Intrahepatic cholestasis of pregnancy has been linked to sudden stillbirth. The suddenness of the stillbirths in these cases have led clinicians to suspect that the pathogenesis of stillbirth in women with intrahepatic cholestasis of preg
Externí odkaz:
https://doaj.org/article/55f8246bd23d42af9d05c46f90d93b85
Autor:
Emmanuel U. Emeasoba, Rodney A. McLaren Jr., Rebecca Landau, Jeremy Weedon, Shoshana Haberman, Howard Minkoff, Jacob Shani, Nadine Montemarano
Publikováno v:
American Journal of Perinatology Reports, Vol 10, Iss 01, Pp e20-e25 (2020)
Objective This study evaluates the assessment of endothelial function and its prediction for preeclampsia among women with high-risk factors. Study Design A prospective cohort study of 107 pregnant women at 20 weeks or greater gestation with risk fac
Externí odkaz:
https://doaj.org/article/2bc2d934823c4a82a056f82b51e5820f
Autor:
Rodney A. McLaren Jr., Kate W.-C. Chang, Nana-Ama E. Ankumah, Lynda J.-S. Yang, Suneet P. Chauhan
Publikováno v:
American Journal of Perinatology Reports, Vol 09, Iss 01, Pp e1-e1 (2019)
Externí odkaz:
https://doaj.org/article/ca63156db1534912a31c63684bfdf5f6
Autor:
Rodney A. McLaren Jr., Kate W.-C. Chang, Nana-Ama E. Ankumah, Lynda J.-S. Yang, Suneet P. Chauhan
Publikováno v:
American Journal of Perinatology Reports, Vol 09, Iss 01, Pp e1-e5 (2019)
Abstract Objective Our objective was to compare persistence of neonatal brachial plexus palsy (NBPP) at 1 and 2 years in children of nulliparous versus parous women. Study Design We conducted a retrospective cohort study of children diagnosed wit
Externí odkaz:
https://doaj.org/article/c199810244e149048f8cf69eca338659
Publikováno v:
American Journal of Perinatology Reports, Vol 08, Iss 04, Pp e349-e354 (2018)
Abstract Objective This study was aimed to evaluate success rates of (1) external cephalic version (ECV) among women with one prior cesarean delivery (CD) and (2) maternal and neonatal outcomes after ECV among women with prior CD. Study Design Tw
Externí odkaz:
https://doaj.org/article/34717b44f16c4880aba1ebb37e1a280c
Autor:
Neel S. Iyer, Matthew H. Mossayebi, Tracy J. Gao, Lylach Haizler‐Cohen, Daniele Di Mascio, Rodney A. McLaren Jr, Huda B. Al‐Kouatly
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Background Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is an X‐linked recessive disorder that predisposes individuals to hemolysis due to an inborn error of metabolism. We performed a systematic literature review to evaluate G6
Externí odkaz:
https://doaj.org/article/1fa8478b3e704473b401189bfd8c3811