Zobrazeno 1 - 10
of 60
pro vyhledávání: '"M. Pruggmayer"'
Publikováno v:
Archives of Gynecology and Obstetrics. 277:155-160
To retrospectively examine the diagnostic accuracy of prenatal RhD blood type genotyping on amniotic fluid, using a combination of two polymerase chain reaction (PCR) methods in daily practice.Amniotic fluid was obtained from women undergoing amnioce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4f87d839131fa05061058602ecbd185
https://doi.org/10.1007/s00404-007-0437-y
https://doi.org/10.1007/s00404-007-0437-y
Autor:
E. Fritzer, G. Kamin, C. S. von Kaisenberg, Franz Bahlmann, M. Bielicki, H. Meyberg, C. Harris, Norbert Arnold, M. Pruggmayer, A. Kossakiewicz, A. Gasiorek-Wiens
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 12:89-94
Objective: To examine the effectiveness of screening for trisomy 21 by a combination of maternal age, fetal nuchal translucency (NT) thickness and maternal serum biochemistry using free β-human cho...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b31950027ec8f42ca6358b96e130fabf
https://doi.org/10.1080/jmf.12.2.89.94
https://doi.org/10.1080/jmf.12.2.89.94
Autor:
W. Seefried, E. Fritzer, J. Klapp, D. Sarlay, F. Bahlmann, U. Germer, H. Meyberg, P. Kuhn, S. Minderer, P. Kozlowski, C. S. von Kaisenberg, M. Bielicki, B. J. Hackelöer, G. Kamin, M. Pruggmayer, A. Kossakiewicz, S. Tercanli, A. Gasiorek-Wiens, K. T. M. Schneider
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 18:645-648
Objective To examine the effectiveness of screening for trisomy 21 by a combination of maternal age and fetal nuchal translucency thickness at 10–14 weeks of gestation in Germany, Austria and Switzerland. Methods This was a multicenter study of scr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fab794323c3230fdb620ec78a73a260
https://doi.org/10.1046/j.0960-7692.2001.00604.x
https://doi.org/10.1046/j.0960-7692.2001.00604.x
Publikováno v:
HNO. 52:258-260
Das velokardiofaziale Syndrom (VCFS) oder Shprintzen-II-Syndrom zeichnet sich v. a. durch Gaumenspalte (69%), Herzfehler (74%), charakteristische faziale Dysmorphien sowie Lernschwierigkeiten (70–90%) aus. Es weist Phanotypuberlappungen mit dem DiG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::987e46f5cdb67db1f096d8a34ed57430
https://doi.org/10.1007/s00106-003-0954-3
https://doi.org/10.1007/s00106-003-0954-3
Publikováno v:
Archives of Gynecology and Obstetrics. 254:160-163
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87d08179ba5d4ef00978a0a2f849acfd
https://doi.org/10.1007/bf02265938
https://doi.org/10.1007/bf02265938
Autor:
M. Schulte-Valentin, Wolfgang Holzgreve, H. Schütte, J. G. Van der Pol, H. Körner, G. Karkut, P. Baumann, R. Lettau, V. F. Duda, M. Pruggmayer, P. Polak, B. Eiben, M. G. J. Jahoda, H. W. Gola, R. Osmers
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 2:6-10
textabstractTo evaluate the risk of abortion after genetic amniocentesis in twin pregnancies, a retrospective study of 15 centers was performed. The spontaneous abortion rate up to 20 completed weeks of gestation was 2.3%; the abortion rate up to 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::631936f9d5af3420c0a0a06c664412fe
https://doi.org/10.1046/j.1469-0705.1992.02010006.x
https://doi.org/10.1046/j.1469-0705.1992.02010006.x
Publikováno v:
Aktuelle Neurologie. 18:216-222
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61b5fe067b6e6f6b74b4838896d681e0
https://doi.org/10.1055/s-2007-1020529
https://doi.org/10.1055/s-2007-1020529
Autor:
M. Wüstemann, Peter Hillemanns, Peter Schmidt, Alexander Scharf, M. Pruggmayer, Holger Maul, C. Sohn, P. Beier, I. Staboulidou
Publikováno v:
Geburtshilfe und Frauenheilkunde. 66
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f26d34b11463682487691695a9cc8ad
https://doi.org/10.1055/s-2006-952879
https://doi.org/10.1055/s-2006-952879
Publikováno v:
Fetal diagnosis and therapy. 21(3)
Objective: To examine the efficacy of first trimester screening for trisomy 21 using a combination of maternal age, fetal nuchal translucency (NT), maternal serum free β-human chorionic gonadotropin (free β-hCG) and pregnancy-associated plasma prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71184bb131c403d3b5bb0f9ac5ce8ba0
https://pubmed.ncbi.nlm.nih.gov/16601335
https://pubmed.ncbi.nlm.nih.gov/16601335
Publikováno v:
HNO. 52(3)
Velocardiofacial syndrome (VCFS) or Shprintzen's syndrome leads to cleft palate (69%), heart defects (74%), and characteristic facial dysmorphies as well as learning difficulties (70-90%). There is phenotypic overlap with DiGeorge syndrome (DGA). In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98563795754e8e60da8db30d09368147
https://pubmed.ncbi.nlm.nih.gov/15004686
https://pubmed.ncbi.nlm.nih.gov/15004686