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Titel:

Association of maternal and/or fetal factor V Leiden and G20210A prothrombin mutation with HELLP syndrome and intrauterine growth restriction.

Dokumenttyp:
Journal Article; Article
Autor(en):
Schlembach, D; Beinder, E; Zingsem, J; Wunsiedler, U; Beckmann, MW; Fischer, T
Abstract:
This study was conducted to investigate the association of maternal and/or fetal factor V Leiden (FVL) and G20210A prothrombin mutation with HELLP syndrome. FVL and G20210A prothrombin mutation were determined using PCR. Sixty-three pregnant women, 36 of them diagnosed with HELLP syndrome, were included in the study. Overall, 68 children were born as a result of these pregnancies and blood sampling was possible in 28 out of 39 children from HELLP patients and 25 out of 29 children from the contr...     »
Zeitschriftentitel:
Clin Sci (Lond)
Jahr:
2003
Band / Volume:
105
Heft / Issue:
3
Seitenangaben Beitrag:
279-85
Sprache:
eng
Volltext / DOI:
doi:10.1042/CS20030073
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/12725641
Print-ISSN:
0143-5221
TUM Einrichtung:
Fachgebiet Perinatalmedizin und Perinatalphysiologie (Prof. Schneider)
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