Search Results - "Wensley, Richard"

Molecular genetic analysis of severe protein C deficiency by Millar, David S., Johansen, Bent, Berntorp, Erik, Minford, Adrian, Bolton-Maggs, Paula, Wensley, Richard, Kakkar, Vijay, Schulman, Sam, Torres, Argimiro, Bosch, Norma, Cooper, David N.

“…Severe protein C deficiency is a rare, early onset, venous thrombotic condition that is inherited as an autosomal recessive trait. The protein C (PROC) genes…”
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Molecular genetic analysis of severe protein C deficiency by MILLAR, D. S, JOHANSEN, B, COOPER, D. N, BERNTORP, E, MINFORD, A, BOLTON-MAGGS, P, WENSLEY, R, KAKKAR, V, SCHULMAN, S, TORRES, A, BOSCH, N

“…Severe protein C deficiency is a rare, early onset, venous thrombotic condition that is inherited as an autosomal recessive trait. The protein C (PROC) genes…”
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Polymerase chain reaction amplification of two polymorphic simple repeat sequences within the von Willebrand factor gene : application to family studies in von Willebrand disease by CUMMING, A. M, ARMSTRONG, J. G, PENDRY, K, BURN, A. M, WENSLEY, R. T

“…We have used the polymerase chain reaction to amplify two variable number of tandem repeats (VNTRs) within a region of repetitive DNA located in intron 40 of…”
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Recurring mutations at CpG dinucleotides in the region of the von Willebrand factor gene encoding the glycoprotein Ib binding domain, in patients with type IIB von Willebrand's disease by Lillicrap, D, Murray, E W, Benford, K, Blanchette, V S, Rivard, G E, Wensley, R, Giles, A R

“…The mutant von Willebrand factor (vWf) molecule in type IIB von Willebrand's disease (vWd) has an increased binding affinity for the platelet receptor…”
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Liver disease in haemophiliacs: an overstated problem? by Stevens, R F, Cuthbert, A C, Perera, P R, Whitwell, H L, Haboubi, N Y, Warnes, T W, Smith, A, Craske, J, Longson, M, Wensley, R T

“…Successful percutaneous liver biopsy was carried out on 12 multi-transfused haemophiliacs from the Manchester area with persistently abnormal liver function…”
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Plasma exchange and human factor VIII concentrate in managing haemophilia A with factor VIII inhibitors by Wensley, R T, Stevens, R F, Burn, A M, Delamore, I W

“…Plasma exchanges were combined with human factor VIII concentrate therapy in the treatment of major bleeding episodes in five patients with haemophilia A and…”
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