Zobrazeno 1 - 8
of 8
pro vyhledávání: '"I C Nitu-Whalley"'
Publikováno v:
Haemophilia. 9:298-302
Determination of the closure time (CT) with the platelet function analyser (PFA-100) is a useful screening test for von Willebrand's disease (VWD) but its role in the characterization of VWD is not well established. We studied the relationship betwee
Publikováno v:
British Journal of Haematology. 108:259-264
This clinical retrospective study investigated the difficulties in diagnosing type 1 von Willebrand disease (VWD). A total of 246 patients previously diagnosed with type 1 VWD were reclassified into 'possible' type 1 VWD (patients with low levels of
Autor:
C A Lee, I C Nitu-Whalley
Publikováno v:
Haemophilia. 5:318-326
Acquired von Willebrand syndrome (AvWS) is a rare bleeding disorder with clinical and laboratory features closely resembling hereditary von Willebrand disease (vWD), arising in previously haemostatically normal individuals. We present a retrospective
Publikováno v:
British journal of haematology. 126(1)
Desmopressin [1-deamino-8-d-arginine vasopressin (DDAVP)] has been successfully used in the treatment of type 1 von Willebrand disease (VWD) and mild haemophilia A (MHA). Data suggest that DDAVP can increase factor XI (FXI) plasma levels and may repr
Autor:
Gulnaz Begum, Robert Marcus, N Duncan, P Mahendra, Sudhir Tauro, P Shankaranarayana, J. I. O. Craig, I C Nitu-Whalley, Charles Craddock
Publikováno v:
Bone marrow transplantation. 32(3)
Stem cell transplantation (SCT) may be the only curative option for patients with relapsed or refractory leukaemia, that is, high-risk (HR) leukaemia. Several salvage regimens have been used to cytoreduce disease before SCT, but disease progression o
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 9(3)
Determination of the closure time (CT) with the platelet function analyser (PFA-100) is a useful screening test for von Willebrand's disease (VWD) but its role in the characterization of VWD is not well established. We studied the relationship betwee
Autor:
I C, Nitu-Whalley, C A, Lee
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 5(5)
Acquired von Willebrand syndrome (AvWS) is a rare bleeding disorder with clinical and laboratory features closely resembling hereditary von Willebrand disease (vWD), arising in previously haemostatically normal individuals. We present a retrospective
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 5(5)
In 1997 the UK Haemophilia Centre Directors Organization published the guidelines for diagnosis and management of von Willebrand disease (vWD). The guidelines stated that desmopressin (DDAVP) should be used in type 1 and type 2N vWD, that it might be