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The diagnosis and management of factor VIII and IX inhibitors : A guideline from the UK Haemophilia Centre Doctors' Organization (UKHCDO)

British journal of haematology, 2000-10, Vol.111 (1), p.78-90

2000

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Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

Journal of thrombosis and haemostasis, 2006-10, Vol.4 (10), p.2103-2114

2006

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Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-03, Vol.16 (2), p.296-304

2010

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Down's syndrome and acute lymphoblastic leukaemia: clinical features and response to treatment

Archives of disease in childhood, 2001-10, Vol.85 (4), p.321-325

2001

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The usefulness of bone marrow aspiration in the diagnosis of Niemann–Pick disease type C in infantile liver disease

Archives of disease in childhood, 2006-10, Vol.91 (10), p.841-844

2006

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The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977–99

Journal of thrombosis and haemostasis, 2004-07, Vol.2 (7), p.1047-1054

2004

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Progressive reduction in treatment‐related deaths in Medical Research Council childhood lymphoblastic leukaemia trials from 1980 to 1997 (UKALL VIII, X and XI)

British journal of haematology, 2001-02, Vol.112 (2), p.293-299

2001

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The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma products

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-11, Vol.17 (6), p.931-937

2011

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Biomass-burning emissions and associated haze layers over Amazonia

Journal of Geophysical Research, 1988-02, Vol.93 (D2), p.1509-1527

1988

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Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-05, Vol.10 (3), p.218-231

2004

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Absence of inhibitors in previously untreated patients with severe haemophilia A after exposure to a single intermediate purity factor VIII product

Thrombosis and haemostasis, 1997-09, Vol.78 (3), p.1027-1029

1997

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The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-05, Vol.10 (3), p.199-217

2004

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Risk reduction strategies for variant Creutzfeldt-Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-03, Vol.16 (2), p.305-315

2010

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A comparison between two semi-quantitative bleeding scales for the diagnosis and assessment of bleeding severity in type 1 von Willebrand disease

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-01, Vol.17 (1), p.165-166

2011

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Epidemiology of Infection with Epstein-Barr Virus Types 1 and 2: Lessons from the Study of a T-Cell-Immunocompromised Hemophilic Cohort

Journal of Virology, 1998-05, Vol.72 (5), p.4352-4363

1998

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A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-11, Vol.16 (6), p.966-969

2010

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Long-term follow-up of the United Kingdom Medical Research Council protocols for childhood acute lymphoblastic leukaemia, 1980-1997

Leukemia, 2000-12, Vol.14 (12), p.2307-2320

2000

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A new candidate missense mutation (Leu 1657 IIe) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease family

Thrombosis and haemostasis, 2000-09, Vol.84 (3), p.369-373

2000

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Recommendations for the treatment of factor VIII inhibitors: from the UK Haemophilia Centre Directors' Organisation Inhibitor Working Party

Blood coagulation & fibrinolysis, 1996-03, Vol.7 (2), p.134-138

1996

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Carbon monoxide and methane over Canada: July–August 1990

Journal of Geophysical Research, 1994-01, Vol.99 (D1), p.1659-1669

1994

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HLA Class II Profile: A Weak Determinant of Factor VIII Inhibitor Development in Severe Haemophilia A

Thrombosis and haemostasis, 1997, Vol.77 (2), p.234-237

1997

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Third and Fourth Workshops of the European paediatric network for haemophilia management

Haemophilia, 2003-03, Vol.9 (2), p.223-228

2003

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Development of local connections in ferret somatosensory cortex

Journal of comparative neurology (1911), 1996-10, Vol.374 (2), p.259-277

1996

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The in vitro development of the pentastomid Porocephalus crotali from the infective instar to the adult stage

Parasitology, 1997-11, Vol.115 (5), p.503-512

1997

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A Mendicant Sermon Collection from Composition to Reception: The Novum opus dominicale of John Waldeby, OESA, by Yuichi Akae

The English historical review, 2017-12, Vol.132 (558), p.1301-1303

Hill, F G

2017

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The diagnosis and management of factor VIII and IX inhibitors : A guideline from the UK Haemophilia Centre Doctors' Organization (UKHCDO)

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophilia

Down's syndrome and acute lymphoblastic leukaemia: clinical features and response to treatment

The usefulness of bone marrow aspiration in the diagnosis of Niemann–Pick disease type C in infantile liver disease

The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977–99

Progressive reduction in treatment‐related deaths in Medical Research Council childhood lymphoblastic leukaemia trials from 1980 to 1997 (UKALL VIII, X and XI)

The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma products

Biomass-burning emissions and associated haze layers over Amazonia

Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

Absence of inhibitors in previously untreated patients with severe haemophilia A after exposure to a single intermediate purity factor VIII product

The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization

Risk reduction strategies for variant Creutzfeldt-Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disorders

A comparison between two semi-quantitative bleeding scales for the diagnosis and assessment of bleeding severity in type 1 von Willebrand disease

Epidemiology of Infection with Epstein-Barr Virus Types 1 and 2: Lessons from the Study of a T-Cell-Immunocompromised Hemophilic Cohort

A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation

Long-term follow-up of the United Kingdom Medical Research Council protocols for childhood acute lymphoblastic leukaemia, 1980-1997

A new candidate missense mutation (Leu 1657 IIe) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease family

Recommendations for the treatment of factor VIII inhibitors: from the UK Haemophilia Centre Directors' Organisation Inhibitor Working Party

Carbon monoxide and methane over Canada: July–August 1990

HLA Class II Profile: A Weak Determinant of Factor VIII Inhibitor Development in Severe Haemophilia A

Third and Fourth Workshops of the European paediatric network for haemophilia management

Development of local connections in ferret somatosensory cortex

The in vitro development of the pentastomid Porocephalus crotali from the infective instar to the adult stage

A Mendicant Sermon Collection from Composition to Reception: The Novum opus dominicale of John Waldeby, OESA, by Yuichi Akae

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