Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Cindy, Hörmansdörfer"'
Autor:
Cindy Hörmansdörfer, Alejandro Corral, Alexander Scharf, Bernhard Vaske, Peter Hillemanns, Peter Schmidt
Publikováno v:
Revista Española de Salud Pública, Vol 84, Iss 1, Pp 43-51 (2010)
Fundamento: En España se ofrece a todas las mujeres gestantes a partir de los 35 años un examen genético a través de un diagnóstico invasivo (indicación por edad materna (IPEM)) para detectar casos fetales de trisomía 21. En la última década
Externí odkaz:
https://doaj.org/article/7e2255bf5c6641e9a5f6bd6415a36b6e
Publikováno v:
Archives of Gynecology and Obstetrics. 283:23-26
Introduction Abnormal yolk sac size is associated with fetal miscarriage. This is a case report of two pregnancies with abnormal yolk sacs. Materials and methods In one case, a twofold sac was found; in the other case, the yolk sac was not of spheric
Publikováno v:
Prenatal diagnosis. 32(2)
A novel screening method for fetal aneuploidies was developed, in which nuchal translucency (NT), pregnancy-associated plasma protein-A (PAPP-A), and free-β human chorionic gonadotropin (free-β hCG) are placed into a three-dimensional scatter plot.
Autor:
Cindy, Hörmansdörfer, Alejandro, Corral, Alexander, Scharf, Bernhard, Vaske, Peter, Hillemanns, Peter, Schmidt
Publikováno v:
Revista espanola de salud publica. 84(1)
In Spain all pregnant women aged 35 years and older are offered genetic examination through invasive testing in order to detect fetal trisomy 21 cases (maternal age indication (MAI)). In the last decade five distinct software programs utilizing the "