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Functional analysis of the classical, alternative, and MBL pathways of the complement system: standardization and validation of a simple ELISA

Journal of immunological methods, 2005, Vol.296 (1), p.187-198

2005

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What Makes an Enterohemorrhagic Escherichia coli?

Clinical infectious diseases, 2006-11, Vol.43 (9), p.1168-1169

2006

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Complement component 5 deficiency (C5D) in South Africa

Molecular immunology, 2011-08, Vol.48 (14), p.1683-1683

2011

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The Yeast Candida albicans Binds Complement Regulators Factor H and FHL-1

Infection and Immunity, 2002-09, Vol.70 (9), p.5185-5192

2002

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The CCP6-8 and CCP19-20 ‘heparin’-binding regions of complement factor H have different and tissue-specific glycosaminoglycan-binding properties

Molecular immunology, 2011-08, Vol.48 (14), p.1716-1717

2011

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Streptococcal inhibitor of complement (SIC) inhibits the membrane attack complex by preventing uptake of C567 onto cell membranes

Immunology, 2001-07, Vol.103 (3), p.390-398

2001

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Screening for Aspergillus spp. using polymerase chain reaction of whole blood samples from patients with haematological malignancies

British journal of haematology, 2001-04, Vol.113 (1), p.180-184

2001

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Complement escape of human pathogenic bacteria by acquisition of complement regulators

Molecular Immunology, 2006, Vol.43 (1), p.31-44

2006

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Utilization and impact of European immunization week to increase measles, mumps, rubella vaccine uptake in Austria in 2016

Vaccine, 2017-09, Vol.35 (37), p.4836-4839

2017

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The Shiga toxin genotype rather than the amount of Shiga toxin or the cytotoxicity of Shiga toxin in vitro correlates with the appearance of the hemolytic uremic syndrome

Diagnostic microbiology and infectious disease, 2007-11, Vol.59 (3), p.235-242

2007

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Long-Term Cytomegalovirus Infection Leads to Significant Changes in the Composition of the CD8+ T-Cell Repertoire, Which May Be the Basis for an Imbalance in the Cytokine Production Profile in Elderly Persons

Journal of Virology, 2005-03, Vol.79 (6), p.3675-3683

2005

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Membranous nephropathy in a patient with hereditary complete complement C4 deficiency

Nephrology, dialysis, transplantation, 2004-04, Vol.19 (4), p.990-993

2004

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Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa

SAMJ: South African Medical Journal, 2012-06, Vol.102 (6), p.525-527

2012

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Immune evasion by acquisition of complement inhibitors: The mould Aspergillus binds both factor H and C4b binding protein

Molecular immunology, 2008-03, Vol.45 (5), p.1485-1493

2008

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Membranoproliferative glomerulonephritis type II (dense deposit disease) : An update

Journal of the American Society of Nephrology, 2005-05, Vol.16 (5), p.1392-1403

2005

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Human Immunodeficiency Virus Type 1 gp160 and gp41 Binding to Candida albicans Selectively Enhances Candidal Virulence In Vitro

The Journal of infectious diseases, 1998-04, Vol.177 (4), p.1057-1063

1998

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Deficiencies of the complement MAC II gene cluster (C6, C7, C9): is subtotal C6 deficiency of particular evolutionary benefit?

Clinical and experimental immunology, 2003-08, Vol.133 (2), p.156-159

Wurzner, R

2003

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Decay‐accelerating factor (CD55) protects human immunodeficiency virus type 1 from inactivation by human complement

European journal of immunology, 1995-01, Vol.25 (1), p.285-290

1995

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Sorbitol-fermenting Shiga toxin-producing Escherichia coli O157: indications for an animal reservoir

Epidemiology and infection, 2006-08, Vol.134 (4), p.719-723

2006

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Compound heterozygous mutations in the C6-gene in a child with relapsing bacterial and viral infections

Molecular immunology, 2013-12, Vol.56 (3), p.298-298

2013

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Evasion of pathogens by avoiding recognition or eradication by complement, in part via molecular mimicry

Molecular Immunology, 1999-03, Vol.36 (4), p.249-260

Wuerzner, R

1999

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Modulation of complement membrane attack by local C7 synthesis

Clinical and experimental immunology, 2000-07, Vol.121 (1), p.8-10

Wurzner, R

2000

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Variability in tellurite resistance and the ter gene cluster among Shiga toxin-producing Escherichia coli isolated from humans, animals and food

Research in microbiology, 2007-03, Vol.158 (2), p.105-111

2007

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The supportive role of complement in HIV pathogenesis

Immunological reviews, 2001-04, Vol.180 (1), p.168-176

2001

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Glomerular deposition of mannose-binding lectin in human glomerulonephritis

Nephrology, dialysis, transplantation, 1999-04, Vol.14 (4), p.881-886

1999

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Functional analysis of the classical, alternative, and MBL pathways of the complement system: standardization and validation of a simple ELISA

What Makes an Enterohemorrhagic Escherichia coli?

Complement component 5 deficiency (C5D) in South Africa

The Yeast Candida albicans Binds Complement Regulators Factor H and FHL-1

The CCP6-8 and CCP19-20 ‘heparin’-binding regions of complement factor H have different and tissue-specific glycosaminoglycan-binding properties

Streptococcal inhibitor of complement (SIC) inhibits the membrane attack complex by preventing uptake of C567 onto cell membranes

Screening for Aspergillus spp. using polymerase chain reaction of whole blood samples from patients with haematological malignancies

Complement escape of human pathogenic bacteria by acquisition of complement regulators

Utilization and impact of European immunization week to increase measles, mumps, rubella vaccine uptake in Austria in 2016

The Shiga toxin genotype rather than the amount of Shiga toxin or the cytotoxicity of Shiga toxin in vitro correlates with the appearance of the hemolytic uremic syndrome

Long-Term Cytomegalovirus Infection Leads to Significant Changes in the Composition of the CD8+ T-Cell Repertoire, Which May Be the Basis for an Imbalance in the Cytokine Production Profile in Elderly Persons

Membranous nephropathy in a patient with hereditary complete complement C4 deficiency

Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa

Immune evasion by acquisition of complement inhibitors: The mould Aspergillus binds both factor H and C4b binding protein

Membranoproliferative glomerulonephritis type II (dense deposit disease) : An update

Human Immunodeficiency Virus Type 1 gp160 and gp41 Binding to Candida albicans Selectively Enhances Candidal Virulence In Vitro

Deficiencies of the complement MAC II gene cluster (C6, C7, C9): is subtotal C6 deficiency of particular evolutionary benefit?

Decay‐accelerating factor (CD55) protects human immunodeficiency virus type 1 from inactivation by human complement

Sorbitol-fermenting Shiga toxin-producing Escherichia coli O157: indications for an animal reservoir

Compound heterozygous mutations in the C6-gene in a child with relapsing bacterial and viral infections

Evasion of pathogens by avoiding recognition or eradication by complement, in part via molecular mimicry

Modulation of complement membrane attack by local C7 synthesis

Variability in tellurite resistance and the ter gene cluster among Shiga toxin-producing Escherichia coli isolated from humans, animals and food

The supportive role of complement in HIV pathogenesis

Glomerular deposition of mannose-binding lectin in human glomerulonephritis

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