Zobrazeno 1 - 10
of 140
pro vyhledávání: '"Brian L, Shaffer"'
Publikováno v:
Clinical Case Reports, Vol 7, Iss 9, Pp 1735-1740 (2019)
Abstract We describe twins with an interstitial deletion of chromosome 1 with a severe phenotype compared to previously described cases. As genetic testing is more frequently performed, it is important for clinicians to understand the spectrum of cli
Externí odkaz:
https://doaj.org/article/99b9fe2349f44cefb5fcf7f8f7a2ecff
Publikováno v:
Prenatal Diagnosis. 40:1517-1524
Objectives Cell-free fetal DNA (cfDNA) has been increasingly incorporated into prenatal aneuploidy screening paradigms given its relatively high sensitivity for Down syndrome (DS). This is often the case when fetal ultrasonographic soft markers are p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c486331ff752f3fcbedf63d62cb06ac6
https://doi.org/10.1002/pd.5803
https://doi.org/10.1002/pd.5803
Autor:
Aaron B. Caughey, Leonardo Pereira, Brendan Kelly, Allison Allen, Erin J. Madriago, Brian L Shaffer, Geske S. Bak
Publikováno v:
Bak, G S, Shaffer, B L, Madriago, E, Allen, A, Kelly, B, Caughey, A B & Pereira, L 2020, ' Detection of fetal cardiac anomalies : cost-effectiveness of increased number of cardiac views ', Ultrasound in Obstetrics and Gynecology, vol. 55, no. 6, pp. 758-767 . https://doi.org/10.1002/uog.21977
Objective To compare the recommended three-view fetal heart screening method to detect major congenital heart disease (CHD) with more elaborate screening strategies to determine the cost-effective strategy in unselected (low-risk) pregnancies. Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13a4a3bbd7ada4454c2ad046a653f753
https://doi.org/10.1002/uog.21977
https://doi.org/10.1002/uog.21977
Autor:
Sage N. Saxton, Brian L Shaffer, Rebecca E. Rdesinski, Lauren Servino, Cori Feist, Amanda J. H. Kim, Stephanie Dukhovny, Sam Bircher
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 35(25)
Congenital anomalies are increasingly diagnosed before birth, which may lead to psychological distress in expectant parents. While the presence of significant symptoms of depression and stress in these parents is established, understanding their cont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17535961a2d1b63b998b7a3761e5ca75
https://pubmed.ncbi.nlm.nih.gov/34670457
https://pubmed.ncbi.nlm.nih.gov/34670457
Publikováno v:
Prenatal diagnosisREFERENCES. 41(11)
OBJECTIVE We investigated the cost-effectiveness of three sequential prenatal cystic fibrosis (CF) carrier screening strategies: genotyping both partners, genotyping one partner then sequencing the second, and sequencing both partners. METHOD A decis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2955bda6034a0fb35e2eeb3e34ba96f7
https://pubmed.ncbi.nlm.nih.gov/34346064
https://pubmed.ncbi.nlm.nih.gov/34346064
Publikováno v:
Clinical Case Reports, Vol 7, Iss 9, Pp 1735-1740 (2019)
Clinical Case Reports
Clinical Case Reports
We describe twins with an interstitial deletion of chromosome 1 with a severe phenotype compared to previously described cases. As genetic testing is more frequently performed, it is important for clinicians to understand the spectrum of clinical fin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04bd8ab5fec25ce11c6d6c17cc6052b9
https://doaj.org/article/99b9fe2349f44cefb5fcf7f8f7a2ecff
https://doaj.org/article/99b9fe2349f44cefb5fcf7f8f7a2ecff
Autor:
Brian L Shaffer, Aaron B. Caughey, Ashley E. Skeith, Maria I. Rodriguez, Karen S. Greiner, Kimberley A. Bullard
Publikováno v:
Obstetrics & Gynecology. 131:581-590
To estimate the effect of 20-week abortion bans on maternal and consequent neonatal health outcomes and costs in the setting of fetal congenital diaphragmatic hernia.A decision-analytic model was built using TreeAge software to evaluate the effect of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd3a3cd5102c6c076e0279e7ad70ba62
https://doi.org/10.1097/aog.0000000000002483
https://doi.org/10.1097/aog.0000000000002483
Autor:
Aaron B. Caughey, Vanessa R. Lee, Brian L Shaffer, Kayli Senz, Whitney M. Humphrey, Jeffrey A. Kuller, Sarah K. Dotters-Katz
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 31:1951-1955
To describe the rate and severity of gestational hypertensive disorders (GHDs) in pregnancies complicated by trisomy 13 (T13).Retrospective cohort study of singleton deliveries in California from 2005 to 2008 using vital statistics and ICD-9 data. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::127e6ada1617835213c68e0d5385abbe
https://doi.org/10.1080/14767058.2017.1332037
https://doi.org/10.1080/14767058.2017.1332037
Publikováno v:
Obstetrics & Gynecology. 135:155S-156S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6a8522028455524a01405a85cac7ac6
https://doi.org/10.1097/01.aog.0000663744.70001.d2
https://doi.org/10.1097/01.aog.0000663744.70001.d2
Publikováno v:
J Matern Fetal Neonatal Med
Objective: Fetuses with genetic copy number variants are poorly detected through traditional prenatal screening. Microdeletions and duplications are clearly identified with diagnostic testing through chromosomal microarray, and screening of a select
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::494ec1aa40cc9a11c31161daf1664c23
https://europepmc.org/articles/PMC7000293/
https://europepmc.org/articles/PMC7000293/
