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A family with type 2M VWD with normal VWF:RCo but reduced VWF:CB and a M1761K mutation in the A3 domain

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-01, Vol.18 (1), p.e33-e33

2012

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Comparison of an immuno-turbidometric method (STalia®d-DI) with an established enzyme linked fluorescent assay (VIDAS®) d-dimer for the exclusion of venous thromboembolism

International journal of laboratory hematology, 2008-06, Vol.30 (3), p.200-204

2008

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Ethnic variation in von Willebrand factor levels can influence the diagnosis of von Willebrand disease

Clinical and laboratory haematology, 2003-08, Vol.25 (4), p.247-249

2003

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International collaborative study to establish the World Health Organization 2nd International Standard for Fibrinogen Concentrate (09/242): communication from the SSC of the ISTH

Journal of thrombosis and haemostasis, 2016-10, Vol.14 (10), p.2068-2072

2016

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Evaluation of a novel ELISA screening test for detection of factor VIII inhibitory antibodies in haemophiliacs

Clinical and laboratory haematology, 1999-04, Vol.21 (2), p.125-128

1999

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Variation in inhibitor reactivity in acquired haemophilia A with different concentrates

Clinical and laboratory haematology, 2000-10, Vol.22 (5), p.287-290

2000

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Value assignment of the WHO 6th International Standard for blood coagulation factor VIII and von Willebrand factor in plasma (07/316)

Journal of thrombosis and haemostasis, 2011-10, Vol.9 (10), p.2100-2102

2011

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A simple inhibitor screen is more sensitive than a Bethesda assay in monitoring for the development of inhibitors in haemophilia A and B

British journal of haematology, 2005-03, Vol.128 (6), p.885-885

2005

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Diagnostic importance of the two‐stage factor VIII:C assay demonstrated by a case of mild haemophilia associated with His1954 → Leu substitution in the factor VIII A3 domain

British journal of haematology, 1999-06, Vol.105 (4), p.1123-1126

1999

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High incidence of defective high-shear platelet function among platelet donors

Transfusion (Philadelphia, Pa.), 2004-05, Vol.44 (5), p.764-770

2004

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Value assignment of the WHO 2nd International Standard von Willebrand factor, concentrate (09/182)

Journal of thrombosis and haemostasis, 2011-08, Vol.9 (8), p.1638-1640

2011

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Evaluation of the von Willebrand factor antigen (vWF-Ag) assay using an immuno-turbidimetric method (STA Liatest® vWF) automated on the MDA®180 coagulometer

Clinical and laboratory haematology, 2000-02, Vol.22 (1), p.29-32

2000

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Factor viii assays in haemophilia a patients treated with refacto

British journal of haematology, 2003-04, Vol.121 (2), p.379-380

2003

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Ethnic variation in von Willebrand factor levels can influence the diagnosis of von Willebrand disease: Ethnic variation in von Willebrand factor levels and diagnosis of von Willebrand disease

Clinical and laboratory haematology, 2003-08, Vol.25 (4), p.247-249

2003

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Diagnostic importance of the two‐stage factor VIII:C assay demonstrated by a case of mild haemophilia associated with His 1954 → Leu substitution in the factor VIII A3 domain

British journal of haematology, 1999-06, Vol.105 (4), p.1123-1126

1999

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Evaluation of the von Willebrand factor antigen (vWF-Ag) assay using an immuno-turbidimetric method (STA Liatest ® vWF) automated on the MDA ® 180 coagulometer: Automated evaluation of vWF-Ag using an immuno-turbometric method

Clinical and laboratory haematology, 2000-02, Vol.22 (1), p.29-32

2000

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P14 Variation in inhibitor reactivity in acquired haemophilia with different concentrates

Blood coagulation & fibrinolysis, 1998-11, Vol.9 (8), p.784

1998

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P11 Evaluation of a novel ELISA screening test for detection of factor VIII inhibitory antibodies in haemophiliacs

Blood coagulation & fibrinolysis, 1998-11, Vol.9 (8), p.782

1998

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Evaluation of a novel ELISA screening test for detection of factor VIII inhibitory antibodies in haemophiliacs: P.G. Martin et al

Clinical and laboratory haematology, 1999-03, Vol.21 (2), p.125-128

1999

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A family with type 2M VWD with normal VWF:RCo but reduced VWF:CB and a M1761K mutation in the A3 domain

Haemophilia : the official journal of the World Federation of Hemophilia, 2012, Vol.18 (1), p.e33-e33

2012

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Nice work

Manufacturing engineer, 1991, Vol.70 (3), p.10

Sukhu, K.A.

1991

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Poor prognosis of bladder cancer patients with occult lymph node metastases treated with neoadjuvant chemotherapy

BJU international, 2018-10, Vol.122 (4), p.627-632

2018

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Rapid, robust, and sustainable antibody responses to mRNA COVID-19 vaccine in convalescent COVID-19 individuals

JCI insight, 2021-10, Vol.6 (20)

2021

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Electroporation-Facilitated Delivery of Plasmid DNA in Skeletal Muscle: Plasmid Dependence of Muscle Damage and Effect of Poloxamer 188

Molecular therapy, 2001-11, Vol.4 (5), p.407-415

2001

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A qualitative study of Latinx parents' experiences of clinical exome sequencing

Journal of genetic counseling, 2020-08, Vol.29 (4), p.574-586

2020

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A family with type 2M VWD with normal VWF:RCo but reduced VWF:CB and a M1761K mutation in the A3 domain

Comparison of an immuno-turbidometric method (STalia®d-DI) with an established enzyme linked fluorescent assay (VIDAS®) d-dimer for the exclusion of venous thromboembolism

Ethnic variation in von Willebrand factor levels can influence the diagnosis of von Willebrand disease

International collaborative study to establish the World Health Organization 2nd International Standard for Fibrinogen Concentrate (09/242): communication from the SSC of the ISTH

Evaluation of a novel ELISA screening test for detection of factor VIII inhibitory antibodies in haemophiliacs

Variation in inhibitor reactivity in acquired haemophilia A with different concentrates

Value assignment of the WHO 6th International Standard for blood coagulation factor VIII and von Willebrand factor in plasma (07/316)

A simple inhibitor screen is more sensitive than a Bethesda assay in monitoring for the development of inhibitors in haemophilia A and B

Diagnostic importance of the two‐stage factor VIII:C assay demonstrated by a case of mild haemophilia associated with His1954 → Leu substitution in the factor VIII A3 domain

High incidence of defective high-shear platelet function among platelet donors

Value assignment of the WHO 2nd International Standard von Willebrand factor, concentrate (09/182)

Evaluation of the von Willebrand factor antigen (vWF-Ag) assay using an immuno-turbidimetric method (STA Liatest® vWF) automated on the MDA®180 coagulometer

Factor viii assays in haemophilia a patients treated with refacto

Ethnic variation in von Willebrand factor levels can influence the diagnosis of von Willebrand disease: Ethnic variation in von Willebrand factor levels and diagnosis of von Willebrand disease

Diagnostic importance of the two‐stage factor VIII:C assay demonstrated by a case of mild haemophilia associated with His 1954 → Leu substitution in the factor VIII A3 domain

Evaluation of the von Willebrand factor antigen (vWF-Ag) assay using an immuno-turbidimetric method (STA Liatest ® vWF) automated on the MDA ® 180 coagulometer: Automated evaluation of vWF-Ag using an immuno-turbometric method

P14 Variation in inhibitor reactivity in acquired haemophilia with different concentrates

P11 Evaluation of a novel ELISA screening test for detection of factor VIII inhibitory antibodies in haemophiliacs

Evaluation of a novel ELISA screening test for detection of factor VIII inhibitory antibodies in haemophiliacs: P.G. Martin et al

A family with type 2M VWD with normal VWF:RCo but reduced VWF:CB and a M1761K mutation in the A3 domain

Nice work

Poor prognosis of bladder cancer patients with occult lymph node metastases treated with neoadjuvant chemotherapy

Rapid, robust, and sustainable antibody responses to mRNA COVID-19 vaccine in convalescent COVID-19 individuals

Electroporation-Facilitated Delivery of Plasmid DNA in Skeletal Muscle: Plasmid Dependence of Muscle Damage and Effect of Poloxamer 188

A qualitative study of Latinx parents' experiences of clinical exome sequencing

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