Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Lucy A. Bayer-Zwirello"'
Autor:
Giulio Genovese, Curtis J. Mello, Po-Ru Loh, Robert E. Handsaker, Seva Kashin, Christopher W. Whelan, Lucy A. Bayer-Zwirello, Steven A. McCarroll
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-15 (2022)
Abstract Non-invasive prenatal testing (NIPT) to detect fetal aneuploidy by sequencing the cell-free DNA (cfDNA) in maternal plasma is being broadly adopted. To detect fetal aneuploidies from maternal plasma, where fetal DNA is mixed with far-larger
Externí odkaz:
https://doaj.org/article/2dcbc97c6abe499b8de027ad8226f55c
Publikováno v:
Operative Obstetrics. :843-873
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3baff4657b8d0b80c9dc5a91ae976f29
https://doi.org/10.1017/cbo9780511580987.031
https://doi.org/10.1017/cbo9780511580987.031
Publikováno v:
Operative Obstetrics. :880-888
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::879db281b90027c74003d28019d7d2e9
https://doi.org/10.1017/cbo9780511580987.033
https://doi.org/10.1017/cbo9780511580987.033
Preclinical regulatory validation of a 3-stage amniotic mesenchymal stem cell manufacturing protocol
Autor:
Jerome Ritz, Lucy A. Bayer-Zwirello, Shaun A. Steigman, Dario O. Fauza, Myriam Armant, Grace Kao, Leslie E. Silberstein
Publikováno v:
Journal of Pediatric Surgery. 43:1164-1169
Purpose Because of the 4 to 6-month interval between a diagnostic amniocentesis and birth, clinical application of amniotic mesenchymal stem cell (AMSC)-based therapies demands a 3-stage cell manufacturing process, including isolation/primary expansi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01f0094a5e11262bdebae183dee4db35
https://doi.org/10.1016/j.jpedsurg.2008.02.052
https://doi.org/10.1016/j.jpedsurg.2008.02.052
Autor:
Camille Kanaan, Gabriel Cohn, Lucy A. Bayer-Zwirello, Rizwan Naeem, Julia Habecker-Green, R. Michael Scott
Publikováno v:
American Journal of Medical Genetics. 94:179-183
We describe a newborn boy one of triplets, whose karyotype was 46,XY,t(8;12)(q22;q21). Prenatal diagnosis of multiple craniofacial anomalies had been made. Following delivery, the patient was thought to exhibit findings consistent with a diagnosis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::591cc7e720f327064a36ec023faaa7d6
https://doi.org/10.1002/1096-8628(20000918)94:3<179::aid-ajmg1>3.0.co
https://doi.org/10.1002/1096-8628(20000918)94:3<179::aid-ajmg1>3.0.co
Successful Treatment of Dermatomyositis During Pregnancy With Intravenous Immunoglobulin Monotherapy
Publikováno v:
Obstetrics & Gynecology. 109:561-563
Background Dermatomyositis is rare during pregnancy and, if untreated, is associated with poor fetal outcome. Corticosteroids are a standard treatment for dermatomyositis in pregnancy, but they have adverse effects. Intravenous immune globulin is an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2881e47babbd07acd81581fb550fab46
https://doi.org/10.1097/01.aog.0000253244.45837.7c
https://doi.org/10.1097/01.aog.0000253244.45837.7c
Autor:
Martin L. Gimovsky, Camille Kanaan, Solveig M.V. Pflueger, John Patrick O'Grady, Lucy A. Bayer-Zwirello, Carol Tunney
Publikováno v:
Journal of Maternal-Fetal and Neonatal Medicine. 1:78-81
Chorioangiomas are common, benign placental tumors that rarely result in perinatal compli- cations unless large or strategically located. A characteristic ultrasonic appearance usually permits easy diagnosis. In the current case, an atypical chorioan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d057cac34cf798b2f55eafeffe8e1857
https://doi.org/10.3109/14767059209161894
https://doi.org/10.3109/14767059209161894
Autor:
Solveig M.V. Pflueger, John Patrick O'Grady, Martin L. Gimovsky, Lucy A. Bayer-Zwirello, Carol Tunney, Camille M. Kanaan, Thomas Carbone
Publikováno v:
Journal of Maternal-Fetal and Neonatal Medicine. 1:70-74
The Beckwith-Wiedemann syndrome (BWS) is a complex congenital disorder with omphalocele, macroglossia, and gigantism as its most common neonatal features. However, in individual cases, the phenotypic expression of this condition is variable. Antenata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54be073873a988549378fc1606e07b38
https://doi.org/10.3109/14767059209161892
https://doi.org/10.3109/14767059209161892
Publikováno v:
Operative Obstetrics ISBN: 9780521681063
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b143edcaab96285af72cda19d73d59a
https://doi.org/10.1017/cbo9780511580987.025
https://doi.org/10.1017/cbo9780511580987.025
