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Range of motion measurements: reference values and a database for comparison studies

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-05, Vol.17 (3), p.500-507

2011

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Peritoneal dialysis adequacy and risk of death

Kidney international, 2000-07, Vol.58 (1), p.446-457

2000

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Prevalence of clinical hip abnormalities in haemophilia A and B: an analysis of the UDC database

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-05, Vol.19 (3), p.426-431

2013

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Incidence of inhibitors in a cohort of 838 males with hemophilia A previously treated with factor VIII concentrates

Journal of thrombosis and haemostasis, 2006-12, Vol.4 (12), p.2576-2581

2006

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The Codevelopment of Community Involvement and Generative Concern Pathways in Emerging and Young Adulthood

Developmental psychology, 2018-10, Vol.54 (10), p.1971-1976

2018

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Validation of Nijmegen–Bethesda assay modifications to allow inhibitor measurement during replacement therapy and facilitate inhibitor surveillance

Journal of thrombosis and haemostasis, 2012-06, Vol.10 (6), p.1055-1061

2012

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Familial clustering of end-stage renal disease in blacks with HIV-associated nephropathy

American journal of kidney diseases, 1999-08, Vol.34 (2), p.254-258

1999

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Comparison of clot‐based, chromogenic and fluorescence assays for measurement of factor VIII inhibitors in the US Hemophilia Inhibitor Research Study

Journal of thrombosis and haemostasis, 2013-07, Vol.11 (7), p.1300-1309

2013

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Complications of haemophilia in babies (first two years of life): a report from the Centers for Disease Control and Prevention Universal Data Collection System

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-03, Vol.23 (2), p.207-214

2017

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Prevalent inhibitors in haemophilia B subjects enrolled in the Universal Data Collection database

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-01, Vol.20 (1), p.25-31

2014

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NHF-McMaster Guideline on Care Models for Haemophilia Management

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-07, Vol.22 (S3), p.6-16

2016

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Healthcare expenditures for males with haemophilia and employer-sponsored insurance in the United States, 2008

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-03, Vol.18 (2), p.268-275

2012

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F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.375-382

2012

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Achievements, challenges and unmet needs for haemophilia patients with inhibitors: Report from a symposium in Paris, France on 20 November 2014

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-01, Vol.22 Suppl 1 (S1), p.1-24

2016

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Relation between Geographic Variability in Kidney Stones Prevalence and Risk Factors for Stones

American journal of epidemiology, 1996-03, Vol.143 (5), p.487-495

1996

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Risk Factors for Candidal Bloodstream Infections in Surgical Intensive Care Unit Patients: The NEMIS Prospective Multicenter Study

Clinical infectious diseases, 2001-07, Vol.33 (2), p.177-186

2001

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The effects of joint disease, inhibitors and other complications on health‐related quality of life among males with severe haemophilia A in the United States

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-07, Vol.23 (4), p.e287-e293

2017

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Prophylaxis use among males with haemophilia B in the United States

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-11, Vol.23 (6), p.910-917

2017

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Health care expenditures for Medicaid-covered males with haemophilia in the United States, 2008

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-03, Vol.18 (2), p.276-283

2012

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Prevalence and risk factors of cardiovascular disease (CVD) events among patients with haemophilia: experience of a single haemophilia treatment centre in the United States (US)

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-07, Vol.17 (4), p.597-604

2011

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The mediating role of cultural coping behaviours on the relationships between academic stress and positive psychosocial well‐being outcomes

International journal of psychology, 2018-10, Vol.53 (S1), p.27-36

2018

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In non‐severe hemophilia A the risk of inhibitor after intensive factor treatment is greater in older patients: a case–control study

Journal of thrombosis and haemostasis, 2010-10, Vol.8 (10), p.2224-2231

2010

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Care models in the management of haemophilia: a systematic review

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-07, Vol.22 (S3), p.31-40

2016

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Sites of initial bleeding episodes, mode of delivery and age of diagnosis in babies with haemophilia diagnosed before the age of 2 years: a report from The Centers for Disease Control and Prevention's (CDC) Universal Data Collection (UDC) project

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-11, Vol.15 (6), p.1281-1290

2009

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PSY15 COSTS OF CARE FOR PRIVATELY INSURED MALES WITH HEMOPHILIA IN THE UNITED STATES, 2008

Value in health, 2011, Vol.14 (3), p.A61-A61

2011

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Range of motion measurements: reference values and a database for comparison studies

Peritoneal dialysis adequacy and risk of death

Prevalence of clinical hip abnormalities in haemophilia A and B: an analysis of the UDC database

Incidence of inhibitors in a cohort of 838 males with hemophilia A previously treated with factor VIII concentrates

The Codevelopment of Community Involvement and Generative Concern Pathways in Emerging and Young Adulthood

Validation of Nijmegen–Bethesda assay modifications to allow inhibitor measurement during replacement therapy and facilitate inhibitor surveillance

Familial clustering of end-stage renal disease in blacks with HIV-associated nephropathy

Comparison of clot‐based, chromogenic and fluorescence assays for measurement of factor VIII inhibitors in the US Hemophilia Inhibitor Research Study

Complications of haemophilia in babies (first two years of life): a report from the Centers for Disease Control and Prevention Universal Data Collection System

Prevalent inhibitors in haemophilia B subjects enrolled in the Universal Data Collection database

NHF-McMaster Guideline on Care Models for Haemophilia Management

Healthcare expenditures for males with haemophilia and employer-sponsored insurance in the United States, 2008

F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity

Achievements, challenges and unmet needs for haemophilia patients with inhibitors: Report from a symposium in Paris, France on 20 November 2014

Relation between Geographic Variability in Kidney Stones Prevalence and Risk Factors for Stones

Risk Factors for Candidal Bloodstream Infections in Surgical Intensive Care Unit Patients: The NEMIS Prospective Multicenter Study

The effects of joint disease, inhibitors and other complications on health‐related quality of life among males with severe haemophilia A in the United States

Prophylaxis use among males with haemophilia B in the United States

Health care expenditures for Medicaid-covered males with haemophilia in the United States, 2008

Prevalence and risk factors of cardiovascular disease (CVD) events among patients with haemophilia: experience of a single haemophilia treatment centre in the United States (US)

The mediating role of cultural coping behaviours on the relationships between academic stress and positive psychosocial well‐being outcomes

In non‐severe hemophilia A the risk of inhibitor after intensive factor treatment is greater in older patients: a case–control study

Care models in the management of haemophilia: a systematic review

Sites of initial bleeding episodes, mode of delivery and age of diagnosis in babies with haemophilia diagnosed before the age of 2 years: a report from The Centers for Disease Control and Prevention's (CDC) Universal Data Collection (UDC) project

PSY15 COSTS OF CARE FOR PRIVATELY INSURED MALES WITH HEMOPHILIA IN THE UNITED STATES, 2008

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