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Preexisting autoantibodies as predictor of immune related adverse events (irAEs) for advanced solid tumors treated with immune checkpoint inhibitors (ICIs)

Oncoimmunology, 2023-12, Vol.12 (1), p.2204754-2204754

2023

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Atypical haemolytic uraemic syndrome and mutations in complement regulator genes

Seminars in immunopathology, 2005-11, Vol.27 (3), p.359-374

2005

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Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome

Journal of the American Society of Nephrology, 2005-02, Vol.16 (2), p.555-563

2005

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Clinical significance of anti-Ro52 (TRIM21) antibodies non-associated with anti-SSA 60 kDa antibodies: Results of a multicentric study

Autoimmunity reviews, 2011-07, Vol.10 (9), p.509-513

2011

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Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

Journal of medical genetics, 2004-06, Vol.41 (6), p.e84-e84

2004

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Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: Report and genetic analysis of 16 cases

Journal of the American Society of Nephrology, 2004-03, Vol.15 (3), p.787-795

2004

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The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts

Journal of medical genetics, 2005-11, Vol.42 (11), p.852-856

2005

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Y402H complement factor H polymorphism associated with exudative age-related macular degeneration in the French population

Molecular vision, 2005-12, Vol.11, p.1135-1140

2005

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Targeting renin-angiotensin system in malignant hypertension in atypical hemolytic uremic syndrome

Indian journal of nephrology, 2017-03, Vol.27 (2), p.136-140

2017

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Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4‐deficient patients with systemic lupus erythematosus (SLE)

Clinical and experimental immunology, 2001-01, Vol.123 (1), p.133-139

2001

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Eculizumab for atypical hemolytic-uremic syndrome in India: First report from India and the challenges faced

Indian journal of nephrology, 2017-01, Vol.27 (1), p.58-61

2017

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Molecular characterization and clinical history of a homozygous functional C1q abnormality

Molecular immunology, 2011-08, Vol.48 (14), p.1722-1722

2011

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Factor H and MCP haplotypes don’t confer susceptibility for C3 glomerulopathy

Molecular immunology, 2011-08, Vol.48 (14), p.1724-1724

2011

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Prevalence of monoclonal gammopathy in patients presenting with acquired angioedema type 2

The American journal of medicine, 2002-08, Vol.113 (3), p.194-199

2002

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Structure-Function-Disease map for the genetic abnormalities in the central complement component C3

Molecular immunology, 2011-08, Vol.48 (14), p.1674-1674

2011

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Anti-factor H auto-antibodies in C3 glomerulopathy

Molecular immunology, 2011-08, Vol.48 (14), p.1724-1724

2011

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High prevalence of hybrid genes involving CFH and CFHR1 in atypical Hemolytic Uremic Syndrome

Molecular immunology, 2011-08, Vol.48 (14), p.1666-1666

2011

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Molecular Basis of a Selective C1s Deficiency Associated with Early Onset Multiple Autoimmune Diseases

The Journal of immunology (1950), 2001-06, Vol.166 (12), p.7612-7616

2001

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Restricted genetic defects underlie human complement C6 deficiency

Clinical and experimental immunology, 2003-04, Vol.132 (1), p.87-91

2003

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Hereditary angio-oedema: effective treatment with the progestogen-only pill in a young woman

British journal of dermatology (1951), 2004-09, Vol.151 (3), p.713-714

2004

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Mutations in complement C3 predispose to development of atypical haemolytic uraemic syndrome

Molecular immunology, 2007-09, Vol.44 (16), p.3923-3923

2007

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Non-Hodgkin's lymphomas and myeloid disorders : deletions associated with t(2;5) and t(3;5) detected by FISH

Leukemia, 1998-07, Vol.12 (7), p.1159-1162

1998

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Expression of low-affinity Fc gamma receptor by a human metastatic melanoma line

Immunology letters, 2000-12, Vol.75 (1), p.1-8

2000

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Quality and best practice in medical laboratories: specific requests for autoimmunity testing

Autoimmunity highlights, 2020-09, Vol.11 (1), p.12, Article 12

2020

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Preexisting autoantibodies as predictor of immune related adverse events (irAEs) for advanced solid tumors treated with immune checkpoint inhibitors (ICIs)

Atypical haemolytic uraemic syndrome and mutations in complement regulator genes

Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome

Clinical significance of anti-Ro52 (TRIM21) antibodies non-associated with anti-SSA 60 kDa antibodies: Results of a multicentric study

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: Report and genetic analysis of 16 cases

The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts

Y402H complement factor H polymorphism associated with exudative age-related macular degeneration in the French population

Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement

Targeting renin-angiotensin system in malignant hypertension in atypical hemolytic uremic syndrome

Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4‐deficient patients with systemic lupus erythematosus (SLE)

Eculizumab for atypical hemolytic-uremic syndrome in India: First report from India and the challenges faced

Molecular characterization and clinical history of a homozygous functional C1q abnormality

Factor H and MCP haplotypes don’t confer susceptibility for C3 glomerulopathy

Prevalence of monoclonal gammopathy in patients presenting with acquired angioedema type 2

Structure-Function-Disease map for the genetic abnormalities in the central complement component C3

Anti-factor H auto-antibodies in C3 glomerulopathy

High prevalence of hybrid genes involving CFH and CFHR1 in atypical Hemolytic Uremic Syndrome

Molecular Basis of a Selective C1s Deficiency Associated with Early Onset Multiple Autoimmune Diseases

Restricted genetic defects underlie human complement C6 deficiency

Hereditary angio-oedema: effective treatment with the progestogen-only pill in a young woman

Mutations in complement C3 predispose to development of atypical haemolytic uraemic syndrome

Non-Hodgkin's lymphomas and myeloid disorders : deletions associated with t(2;5) and t(3;5) detected by FISH

Expression of low-affinity Fc gamma receptor by a human metastatic melanoma line

Quality and best practice in medical laboratories: specific requests for autoimmunity testing

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