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1.685 Aktuelle Fachpublikationen aus der Branche Diagnostik
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16.01.2018 | S. Schwartz, M. Kohan, R. Pasion, P.R. Papenhausen, L.D. Platt, Prenatal Diagnosis, 2018
Abstract Objective Screening via non‐invasive prenatal testing (NIPT) involving the analysis of cell‐free DNA (cfDNA) from plasma has become readily available to screen for chromosomal and DNA aberrations through maternal blood. This report reviews a laboratory's experience with follow‐up of ...
16.01.2018 | Alexander Kucherov, Jessica Atrio, Zev Williams, Prenatal Diagnosis, 2018
Abstract Objective To determine how frequently and effectively products of conception can be obtained among women pursuing medical management of early pregnancy loss. Methods This pilot study was conducted to assess products of conception recovery outcomes for participants opting for ...
15.01.2018 | Kun Sun, Fiona M.F. Lun, Tak Y. Leung, Rossa W.K. Chiu, Y.M. Dennis Lo, Hao Sun, Prenatal Diagnosis, 2018
Abstract Objective During human pregnancy, the DNA methylation of placental tissue is highly relevant to the normal growth and development of the fetus, therefore methylomic analysis of the placental tissue possesses high research and clinical value in prenatal testing and monitoring. Thus ...
12.01.2018 | Kevin G. Friedman, Lynn A. Sleeper, Raina N. Fichorova, Taylor Weilnau, Wayne Tworetzky, Louise E. Wilkins‐Haug, Prenatal Diagnosis, 2018
Abstract Objective Fetal aortic stenosis (AS) imposes pressure load on the developing left ventricle (LV) and leads to derangements in myocardial structure and function via mechanisms that are not well characterized. Methods We compared amniotic fluid NT‐BNP and troponin levels in ...
12.01.2018 | Hagit Daum, Israela Lerer, Ayala Frumkin, Daniel Rosenak, Nili Yanai, Shay Porat, Simcha Yagel, Vardiella Meiner, Prenatal Diagnosis, 2018
Abstract Objectives Chromosomal microarray (CMA) analysis is effectively applied prenatally to detect copy number changes. SNP probes included in the microarray platform can detect regions of excessive homozygosity (ROH) and identical‐by‐descent genomic stretches. The utility of the latter ...
12.01.2018 | Hagit Daum, Israela Lerer, Ayala Frumkin, Daniel Rosenak, Nili Yanai, Shay Porat, Simcha Yagel, Vardiella Meiner, Prenatal Diagnosis, 2018
Abstract Objectives Chromosomal microarray (CMA) analysis is effectively applied prenatally to detect copy number changes. SNP probes included in the microarray platform can detect regions of excessive homozygosity (ROH) and identical‐by‐descent genomic stretches. The utility of the latter ...
10.01.2018 | Adam J. Wolfberg, Prenatal Diagnosis, 2018
Abstract Authors of policy statements from the American College of Obstetrics and Gynecology and from the Society for Maternal‐Fetal Medicine do not acknowledge the potential for their clinical income to influence their opinions, or the positions of the societies they represent. These policy ...
09.01.2018 | Sara B. Hay, Trilochan Sahoo, Mary K. Travis, Karine Hovanes, Natasa Dzidic, Charles Doherty, Michelle N. Strecker, Prenatal Diagnosis, 2018
Abstract Objective The American College of Obstetricians and Gynecologists (ACOG) and Society for Maternal‐Fetal Medicine (SMFM) recommend chromosomal microarray analysis (CMA) for prenatal diagnosis in cases with one or more fetal structural abnormalities. For patients who elect prenatal ...
05.01.2018 | Sharon Perlman, Lucia Roitman, Danny Lotan, Zvi Kivilevitch, Benjamin Dekel, Naomi Pode‐Shakked, Ben Pode‐Shakked, R ..., Prenatal Diagnosis, 2018
Abstract Objective To focus on fetuses diagnosed with severe hydronephrosis and correlate pre‐natal sonographic characteristics with post‐natal outcome. Methods Cases presenting prenatally with severe hydronephrosis (APRPD) >15 mm) were collected retrospectively over a period of 11 ...
05.01.2018 | Eunice Ka Long Chiu, Winnie Wai In Hui, Rossa Wai Kwun Chiu, Prenatal Diagnosis, 2018
Abstract Cell‐free fetal DNA analysis for non‐invasive prenatal screening of fetal chromosomal aneuploidy has been widely adopted for clinical use. Fetal monogenic diseases have also been shown to be amenable to non‐invasive detection by maternal plasma DNA analysis. A number of recent ...
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