Kaser EG: Genotyp-Phänotyp-Korrelation beim leichten hereditären ...

84
Narang GS, Arora S, Pahwa JS. Combined Factor VII and X Deficiency. Online J Health
Allied Scs. 2010; 9: 17
Nawroth F, Strehler E, Sterzik K, Ludwig M. Habituelle Aborte –Diagnostik und Therapie.
Frauenarzt 2006; 47: 300-304
Novo Nordisk Pharma GmbH, Online Fachinformation zu NovoSeven® 2012.
www.novonordisk.de/prodocs/Fachinfo/NovoSeven.pdf (Zugriffsdatum 12.01.2013)
O’Hara PJ, Grant FJ, Haldemann BA, Cray CL, Insley MY, Hagen FS, Murray MJ.
Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent
protein participating in blood coagulation. Proc Natl Acad Sci USA1987; 84: 5158−5162
Oldenburg J, Barthels M. Angeborene Koagulopathien am Beispiel der Hämophilie A
und B, Hemmkörperhämophilie; Hämostaseologie 2008; 28: 353−347
Perry DJ, Haemophilia Centre and Haemostasis Unit, Royal Free and University College
Medical School, London. Factor VII deficiency: Review. Br. J. Haematol. 2002; 118:
689−700
Peyvandi F, Palla R, Menegatti M, Molosio S, Universität Mailand, 2010: Rare Bleeding
Disorders. http://www.rbdd.org/image/books/German.pdf (Zugriffsdatum 30.08.2011)
Peyvandi F, Bianchi-Bonomi A, Luigi Villa Foundation, IRCSS Maggiore Hospital,
Mangiagalli and Regina Elena Foundation, University of Milan, Hemophilia and
Thrombosis Centre, 2011: Rare bleeding disorders database. http://www.rbdd.org
(Zugriffsdatum 30.08.2011)
Peyvandi F, Mannucci PM, Asti D, Abdoullahi M, Di Rocco N und Perry DJ (1997)
Clinical manifestations in 28 Italian and Iranian patients with severe Factor VII deficiency.
Haemophilia 1997; 3: 242–246