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NovoSeven® (Recombinant Factor VIla) in Central Nervous System Bleeds

Pathophysiology of haemostasis and thrombosis, 1996, Vol.26 (Suppl. 1), p.131-134

1996

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Characterization of a causative mutation of hemophilia A identified in the promoter region of the factor VIII gene (F8)

Journal of thrombosis and haemostasis, 2008-01, Vol.6 (1), p.193-195

2008

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The identification and classification of 41 novel mutations in the factor VIII gene (F8C)

Human mutation, 2002-03, Vol.19 (3), p.274-278

2002

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HYPOTHYROIDISM AS A CAUSE OF ACQUIRED VON WDLLEBRAND'S DISEASE

The Lancet (British edition), 1987-05, Vol.329 (8540), p.1007-1009

1987

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A new-generation dilute Russell's viper venom time assay system for lupus anticoagulants: evaluation of detection utilising frozen reagents and controls

British journal of biomedical science, 2005-01, Vol.62 (3), p.127-132

2005

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Low frequency of elevated prothrombin times in patients with lupus anticoagulants when using a recombinant thromboplastin reagent: implications for dosing and monitoring of oral anticoagulant therapy

British journal of biomedical science, 2005-01, Vol.62 (1), p.15-18

2005

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TRANSMISSION OF NON-A, NON-B HEPATITIS BY HEAT-TREATED FACTOR VIII CONCENTRATE

The Lancet (British edition), 1985-07, Vol.326 (8445), p.1-4

1985

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2424 The role of the retinal vascular endothelium in cellular trafficking in EAU in vivo

Vision research (Oxford), 1995-10, Vol.35, p.S113

1995

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Absence of the y-Leu 427 (y) Variant in the Platelet Granular Fibrinogen Pool Supports the Role of Glycoprotein IIB IIIA in Mediating Fibrinogen Uptake into Platelets Megakaryocytes

Blood, 1992-06, Vol.79 (12), p.3394-3394

1992

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2424 The role of the retinal vascular endothelium in cellular trafficking in EAU [formula omitted]

Vision research (Oxford), 1995, Vol.35, p.S113-S113

1995

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Phast assessment of vWF:Ag multimeric distribution

Thrombosis research, 1990-07, Vol.59 (2), p.369-373

1990

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Recombinant factor VIIa (r-FVIIa) in haemophilia management

Transfusion science, 1996-09, Vol.17 (3), p.339-340

1996

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Platelet hyperggregabillity in two patients killinefelter's sundrome complicated by leg ulcers

British journal of dermatology (1951), 1989-02, Vol.120 (2), p.322-322

1989

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A new rapid semi-dry blotting technique for multimeric sizing of von willebrand factor

Thrombosis research, 1988-04, Vol.50 (2), p.345-349

1988

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HTLV-III RELATED ILLNESS AND CHRISTMAS DISEASE

The Lancet (British edition), 1986-02, Vol.327 (8478), p.447-448

1986

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Chromatography of the VIII/VWF complex on dextran sulphate sepharose

Thrombosis research, 1988-04, Vol.50 (2), p.295-304

1988

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Chromatography of vWF on dextran sulphate sepharose

Thrombosis research, 1987-12, Vol.48 (6), p.641-652

1987

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WET HEATING FOR SAFER FACTOR VIII CONCENTRATE?

The Lancet (British edition), 1985-09, Vol.326 (8457), p.721-721

1985

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Combined von Willebrand's disease and factor XII deficiency in a carrier of haemophilia B

Clinical and laboratory haematology, 1989, Vol.11 (2), p.139-141

1989

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Surgical Management of Genu Varum Complicating Haemophilic Arthropathy of the Knee

Pathophysiology of haemostasis and thrombosis, 1981, Vol.10 (Suppl. 1), p.220-220

1981

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Von Willebrand factor has more than one binding site for platelets

Thrombosis research, 1984-06, Vol.34 (5), p.361-366

1984

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An optimized radioimmunoassay of F VIII related antigen (F VIIIR:AG) in plasma and eluates

Thrombosis research, 1979-02, Vol.14 (2), p.363-376

1979

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Combination therapy of steroids and immunoglobulin in chronic refractory idiopathic thrombocytopenic purpura (ITP) enabling renal stone fragmentation by lithotripsy

Clinical and laboratory haematology, 1986-12, Vol.8 (4), p.315-319

1986

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The Effects of Amrinone on Platelet Count, Survival and Function

Clinical science (1979), 1983-02, Vol.64 (2), p.7-7P

1983

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Combined von Willebrand's disease and factor XII deficiency in a carrier of haemophilia B

Clinical & Laboratory Haematology, 1989, Vol.11 (2), p.139-141

1989

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NovoSeven® (Recombinant Factor VIla) in Central Nervous System Bleeds

Characterization of a causative mutation of hemophilia A identified in the promoter region of the factor VIII gene (F8)

The identification and classification of 41 novel mutations in the factor VIII gene (F8C)

HYPOTHYROIDISM AS A CAUSE OF ACQUIRED VON WDLLEBRAND'S DISEASE

A new-generation dilute Russell's viper venom time assay system for lupus anticoagulants: evaluation of detection utilising frozen reagents and controls

Low frequency of elevated prothrombin times in patients with lupus anticoagulants when using a recombinant thromboplastin reagent: implications for dosing and monitoring of oral anticoagulant therapy

TRANSMISSION OF NON-A, NON-B HEPATITIS BY HEAT-TREATED FACTOR VIII CONCENTRATE

2424 The role of the retinal vascular endothelium in cellular trafficking in EAU in vivo

Absence of the y-Leu 427 (y) Variant in the Platelet Granular Fibrinogen Pool Supports the Role of Glycoprotein IIB IIIA in Mediating Fibrinogen Uptake into Platelets Megakaryocytes

2424 The role of the retinal vascular endothelium in cellular trafficking in EAU [formula omitted]

Phast assessment of vWF:Ag multimeric distribution

Recombinant factor VIIa (r-FVIIa) in haemophilia management

Platelet hyperggregabillity in two patients killinefelter's sundrome complicated by leg ulcers

A new rapid semi-dry blotting technique for multimeric sizing of von willebrand factor

HTLV-III RELATED ILLNESS AND CHRISTMAS DISEASE

Chromatography of the VIII/VWF complex on dextran sulphate sepharose

Chromatography of vWF on dextran sulphate sepharose

WET HEATING FOR SAFER FACTOR VIII CONCENTRATE?

Combined von Willebrand's disease and factor XII deficiency in a carrier of haemophilia B

Surgical Management of Genu Varum Complicating Haemophilic Arthropathy of the Knee

Von Willebrand factor has more than one binding site for platelets

An optimized radioimmunoassay of F VIII related antigen (F VIIIR:AG) in plasma and eluates

Combination therapy of steroids and immunoglobulin in chronic refractory idiopathic thrombocytopenic purpura (ITP) enabling renal stone fragmentation by lithotripsy

The Effects of Amrinone on Platelet Count, Survival and Function

Combined von Willebrand's disease and factor XII deficiency in a carrier of haemophilia B

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