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Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub‐Saharan Africa: implications for the susceptibility to meningococcal disease

Clinical and experimental immunology, 2017-08, Vol.189 (2), p.226-231

2017

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Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans

Clinical and experimental immunology, 2012-03, Vol.167 (3), p.459-471

2012

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Methotrexate, Doxorubicin, and Cisplatin (MAP) Plus Maintenance Pegylated Interferon Alfa-2b Versus MAP Alone in Patients With Resectable High-Grade Osteosarcoma and Good Histologic Response to Preoperative MAP: First Results of the EURAMOS-1 Good Response Randomized Controlled Trial

Journal of clinical oncology, 2015-07, Vol.33 (20), p.2279-2287

2015

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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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Characterization of a large genomic deletion in four Irish families with C7 deficiency

Molecular immunology, 2012-02, Vol.50 (1-2), p.57-59

2012

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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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SOUTH AFRICAN PATIENTS WITH GENETIC DEFICIENCIES OF COMPLEMENT COMPONENTS C5 AND C6 SUFFER A MARKED INCREASE IN SUSCEPTIBILITY TO MENINGOCOCCAL DISEASE

Current allergy & clinical immunology, 2015-09, Vol.28 (3), p.192-194

2015

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Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects

Clinical and experimental immunology, 2000-02, Vol.119 (2), p.255-258

Orren, A

2000

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Screening for complement deficiency

Methods in molecular biology (Clifton, N.J.), 2000, Vol.150, p.139

Orren, A

2000

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The Cambridge Companion to the United States Constitution

2018

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Vaccination against meningococcus in complement‐deficient individuals

Clinical and experimental immunology, 1998-12, Vol.114 (3), p.327-329

1998

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How do mammals distinguish between pathogens and non-self?

Trends in microbiology (Regular ed.), 1996-07, Vol.4 (7), p.254-257

Orren, Ann

1996

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Complement‐mediated lipopolysaccharide release and outer membrane damage in Escherichia coli J5: requirement for C9

Immunology, 2001-03, Vol.102 (3), p.365-372

2001

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The molecular basis of C6 deficiency in the western Cape, South Africa

Human genetics, 1998-10, Vol.103 (4), p.506-512

1998

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Elites and the Idea of Equality: A Comparison of Japan, Sweden, and the United States

1, 1990

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Meningococcal septicaemia in a C6-deficient patient and effects of plasma transfusion on lipopolysaccharide release

The Lancet (British edition), 1992-12, Vol.340 (8832), p.1379-1381

1992

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South African patients with genetic deficiencies of complement components C5 and C6 suffer a marked increase in susceptibility to meningococcal disease : invited review

Current allergy & clinical immunology, 2015-09, Vol.28 (3), p.192-194

2015

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Characterization of strains of Neisseria meningitidis recovered from complement-sufficient and complement-deficient patients in the Western Cape Province, South Africa

Journal of Clinical Microbiology, 1994-09, Vol.32 (9), p.2185-2191

1994

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C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish

Clinical and experimental immunology, 1998-12, Vol.114 (3), p.355-361

1998

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

South African medical journal, 2012-06, Vol.102 (6), p.525-527

2012

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Complement component C7 deficiency in four Irish families: The characterisation of a large genomic deletion within the C7 gene

Molecular immunology, 2009-09, Vol.46 (14), p.2870-2870

2009

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Index

The Cambridge Companion to the United States Constitution, 2018, p.489-508

Orren, Karen

2018

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The Cambridge Companion to the United States Constitution

The Cambridge Companion to the United States Constitution, 2018, p.i-ii

Orren, Karen

2018

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Contributors

The Cambridge Companion to the United States Constitution, 2018, p.vii-viii

Orren, Karen

2018

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Acknowledgments

The Cambridge Companion to the United States Constitution, 2018, p.ix-x

Orren, Karen

2018

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Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub‐Saharan Africa: implications for the susceptibility to meningococcal disease

Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans

Methotrexate, Doxorubicin, and Cisplatin (MAP) Plus Maintenance Pegylated Interferon Alfa-2b Versus MAP Alone in Patients With Resectable High-Grade Osteosarcoma and Good Histologic Response to Preoperative MAP: First Results of the EURAMOS-1 Good Response Randomized Controlled Trial

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

Characterization of a large genomic deletion in four Irish families with C7 deficiency

Complement component 5 deficiency (C5D) in South Africa

SOUTH AFRICAN PATIENTS WITH GENETIC DEFICIENCIES OF COMPLEMENT COMPONENTS C5 AND C6 SUFFER A MARKED INCREASE IN SUSCEPTIBILITY TO MENINGOCOCCAL DISEASE

Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects

Screening for complement deficiency

The Cambridge Companion to the United States Constitution

Vaccination against meningococcus in complement‐deficient individuals

How do mammals distinguish between pathogens and non-self?

Complement‐mediated lipopolysaccharide release and outer membrane damage in Escherichia coli J5: requirement for C9

The molecular basis of C6 deficiency in the western Cape, South Africa

Elites and the Idea of Equality: A Comparison of Japan, Sweden, and the United States

Meningococcal septicaemia in a C6-deficient patient and effects of plasma transfusion on lipopolysaccharide release

South African patients with genetic deficiencies of complement components C5 and C6 suffer a marked increase in susceptibility to meningococcal disease : invited review

Characterization of strains of Neisseria meningitidis recovered from complement-sufficient and complement-deficient patients in the Western Cape Province, South Africa

C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish

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

Complement component C7 deficiency in four Irish families: The characterisation of a large genomic deletion within the C7 gene

Index

The Cambridge Companion to the United States Constitution

Contributors

Acknowledgments

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