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Transfusion-associated circulatory overload in Ireland: a review of cases reported to the National Haemovigilance Office 2000 to 2010

Transfusion (Philadelphia, Pa.), 2015-06, Vol.55 (6), p.1223-1230

2015

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Innate immune genes synergize to predict increased risk of chronic disease in hepatitis C virus infection

Proceedings of the National Academy of Sciences - PNAS, 2011-04, Vol.108 (14), p.5736-5741

2011

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Long-Term Evolution of the Hypervariable Region of Hepatitis C Virus in a Common-Source-Infected Cohort

Journal of Virology, 1998-06, Vol.72 (6), p.4893-4905

1998

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Additive effects of HLA alleles and innate immune genes determine viral outcome in HCV infection

Gut, 2015-05, Vol.64 (5), p.813-819

2015

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Distinct MHC class I and II alleles are associated with hepatitis C viral clearance, originating from a single source

Hepatology (Baltimore, Md.), 2004-07, Vol.40 (1), p.108-114

2004

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Outcome of an optional HCV screening program for blood transfusion recipients in Ireland

Transfusion (Philadelphia, Pa.), 2002-11, Vol.42 (11), p.1501-1506

2002

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Transfusion Associated Circulatory Overload (TACO) Incidence and Risk Factors

Blood, 2009-11, Vol.114 (22), p.3157-3157

2009

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The origin of hepatitis C virus genotypes

Journal of general virology, 1997-02, Vol.78 (2), p.321-328

1997

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Chronic hepatitis C infection and sicca syndrome: a clear association with HLA DQB102

European journal of gastroenterology & hepatology, 2007-06, Vol.19 (6), p.493-498

2007

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The value of autofluorescence as a diagnostic feature of acute promyelocytic leukemia

Haematologica (Roma), 2006-03, Vol.91 (3), p.417-418

2006

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The MHC is a major determinant of viral status, but not fibrotic stage, in individuals infected with hepatitis C

Gastroenterology (New York, N.Y. 1943), 2000-06, Vol.118 (6), p.1124-1130

2000

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Modelling infectious disease transmission with complex exposure pattern and sparse outcome data

Statistics in medicine, 2004-10, Vol.23 (19), p.3013-3032

2004

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Haemovigilance

Vox sanguinis, 2006-04, Vol.90 (3), p.207-241

2006

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Clinical Outcomes after Hepatitis C Infection from Contaminated Anti-D Immune Globulin

The New England journal of medicine, 1999-09, Vol.341 (10), p.762-763

1999

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Variation of hepatitis C virus following serial transmission: multiple mechanisms of diversification of the hypervariable region and evidence for convergent genome evolution

Journal of general virology, 1999-03, Vol.80 (3), p.717-725

1999

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Hepatitis C infection from anti-D immunoglobulin

The Lancet (British edition), 1995-08, Vol.346 (8971), p.372-373

1995

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Association of celiac disease with microsatellite polymorphisms close to the tumor necrosis factor genes

Human immunology, 1996, Vol.45 (1), p.24-31

1996

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Setting Up the Hemovigilance Scheme in Ireland

Transfusion alternatives in tranfusion medicine, 2003-04, Vol.5 (1), p.266-271

2003

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A Second Outbreak of Hepatitis C Virus Infection from Anti–D Immunoglobulin in Ireland

Vox sanguinis, 1999-03, Vol.76 (3), p.175-180

1999

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An Outbreak of Hepatitis A among Irish Haemophiliacs

International journal of epidemiology, 1995-08, Vol.24 (4), p.821-828

1995

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A Second Outbreak of Hepatitis C Virus Infection from Anti-D Immunoglobulin in Ireland

Vox sanguinis, 1999-04, Vol.76 (3), p.175-180

1999

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Non-toxic DNA extraction in a clinical setting

Leukemia research, 1994-06, Vol.18 (6), p.469-471

1994

Volltextzugriff (PDF)

Non‐radioactive detection of immunoglobulin and T cell receptor gene rearrangement in acute lymphoblastic leukaemia

British journal of haematology, 1991-11, Vol.79 (3), p.516-519

1991

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Megakaryoblastic Leukemia Presenting as Acute Myelofibrosis—A Study of Four Cases With the Platelet-Peroxidase Reaction

Blood, 1981-08, Vol.58 (2), p.206-213

1981

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A new human plasma cell line, Karpas 620, with translocations involving chromosomes 1, 11 and 14

British journal of haematology, 1990-01, Vol.74 (1), p.70-76

1990

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Transfusion-associated circulatory overload in Ireland: a review of cases reported to the National Haemovigilance Office 2000 to 2010

Innate immune genes synergize to predict increased risk of chronic disease in hepatitis C virus infection

Long-Term Evolution of the Hypervariable Region of Hepatitis C Virus in a Common-Source-Infected Cohort

Additive effects of HLA alleles and innate immune genes determine viral outcome in HCV infection

Distinct MHC class I and II alleles are associated with hepatitis C viral clearance, originating from a single source

Outcome of an optional HCV screening program for blood transfusion recipients in Ireland

Transfusion Associated Circulatory Overload (TACO) Incidence and Risk Factors

The origin of hepatitis C virus genotypes

Chronic hepatitis C infection and sicca syndrome: a clear association with HLA DQB102

The value of autofluorescence as a diagnostic feature of acute promyelocytic leukemia

The MHC is a major determinant of viral status, but not fibrotic stage, in individuals infected with hepatitis C

Modelling infectious disease transmission with complex exposure pattern and sparse outcome data

Haemovigilance

Clinical Outcomes after Hepatitis C Infection from Contaminated Anti-D Immune Globulin

Variation of hepatitis C virus following serial transmission: multiple mechanisms of diversification of the hypervariable region and evidence for convergent genome evolution

Hepatitis C infection from anti-D immunoglobulin

Association of celiac disease with microsatellite polymorphisms close to the tumor necrosis factor genes

Setting Up the Hemovigilance Scheme in Ireland

A Second Outbreak of Hepatitis C Virus Infection from Anti–D Immunoglobulin in Ireland

An Outbreak of Hepatitis A among Irish Haemophiliacs

A Second Outbreak of Hepatitis C Virus Infection from Anti-D Immunoglobulin in Ireland

Non-toxic DNA extraction in a clinical setting

Non‐radioactive detection of immunoglobulin and T cell receptor gene rearrangement in acute lymphoblastic leukaemia

Megakaryoblastic Leukemia Presenting as Acute Myelofibrosis—A Study of Four Cases With the Platelet-Peroxidase Reaction

A new human plasma cell line, Karpas 620, with translocations involving chromosomes 1, 11 and 14

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