Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sonja Krey"'
Autor:
Pier Mannuccio Mannucci, Sonja Krey, Francesco Rodeghiero, Augusto B. Federici, Rainer Zimmermann, Elke Drewke, Giancarlo Castaman, Gabi Riesen, Barbara Zieger, Ulrich Budde, Reinhard Schneppenheim
Publikováno v:
Thrombosis and Haemostasis. 83:136-140
SummaryVon Willebrand disease type 2M “Vicenza” (VWD 2M V) is characterised by autosomal dominant inheritance, low von Willebrand factor (VWF) and the presence of “supranormal” multimers in plasma. This specific phenotype has been described i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cc54880c9a6982f0904fb51af1421d8
https://doi.org/10.1055/s-0037-1613769
https://doi.org/10.1055/s-0037-1613769
Autor:
Johannes Oldenburg, Rainer Schwaab, Sonja Krey, Ulrich Budde, Elke Drewke, Frauke Bergmann, Reinhard Schneppenheim, Eberhard Lechler
Publikováno v:
Thrombosis and Haemostasis. 76:598-602
SummaryA screening program for the detection of patients with von Willebrand disease type 2N (VWD 2N) was carried out in 177 unrelated patients previously diagnosed with haemophilia A and in 199 unrelated patients with VWD type 1 in comparison. By me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11950f1d20b313b0a7084aaa118e01fc
https://doi.org/10.1055/s-0038-1650628
https://doi.org/10.1055/s-0038-1650628
Autor:
Ursula Jessat, Anton H. Sutor, Sonja Krey, Ulrich Budde, Barbara Zieger, Reinhard Schneppenheim, Kathy B. Thomas
Publikováno v:
Human genetics. 95(6)
A screening project to identify candidate molecular defects causing von Willebrand disease type IIC (VWD IIC) in a German family was carried out using polymerase chain reaction (PCR) amplification of all 52 exons of the von Willebrand factor (VWF) ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd785e4ccd9a54720896ee15b4d3f7ba
https://pubmed.ncbi.nlm.nih.gov/7789955
https://pubmed.ncbi.nlm.nih.gov/7789955
Autor:
Dietrich Bock, Frauke Bergmann, Eva Simeoni, Uwe Mittler, Klaus Olek, Günter Mertes, Sonja Krey, Reinhard Schneppenheim, Ulrich Budde, Esther Meili, Hansjörg Plendl, Malte Lange, Richard Linde
Publikováno v:
Human Genetics. 94
The genetic heterogeneity of severe von Willebrand disease (vWd) type III was estimated by analysing extended haplotypes of eleven intragenic restriction fragment length polymorphisms and one variable number of tandem repeat polymorphism in 32 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22547d0e698f77b9c2ceb6c0d044089a
https://doi.org/10.1007/bf00206958
https://doi.org/10.1007/bf00206958
Autor:
Pamela Dickinson, Michael J. Denton, Christine Duvigneau, Sonja Krey, Sigrid Bartkowski, Holger Kranich, Andreas Gal
Publikováno v:
Human molecular genetics. 2(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::675fb71cebe39397f7ef632d880a8289
https://pubmed.ncbi.nlm.nih.gov/8353500
https://pubmed.ncbi.nlm.nih.gov/8353500