Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Lupus diseases associated with hereditary and acquired deficiencies of complement.

× No keyword cloud information.

92 in total

1. Cutaneous immunopathology: recent observations.

Authors: D L Tuffanelli
Journal: J Invest Dermatol Date: 1975-07 Impact factor: 8.551

2. Heterogeneity of the clinical syndrome in patients with systemic lupus erythematosus and genetic deficiency of the second complement component.

Authors: R I Rynes; R E Urizar; R J Pickering
Journal: Clin Exp Immunol Date: 1978-04 Impact factor: 4.330

3. Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies.

Authors: S I Rosenfeld; M E Kelly; J P Leddy
Journal: J Clin Invest Date: 1976-06 Impact factor: 14.808

4. Characterization of a non-functional form of C1q found in patients with a genetically linked deficiency of C1q activity.

Authors: K B Reid; R A Thompson
Journal: Mol Immunol Date: 1983-10 Impact factor: 4.407

5. Homozygous C2 deficiency, lupus erythematosus, and anti-Ro (SSA) antibodies.

Authors: T T Provost; F C Arnett; M Reichlin
Journal: Arthritis Rheum Date: 1983-10

6. Hereditary C2 deficiency in systemic lupus erythematosus and acquired complement abnormalities in an unusual SLE-related syndrome.

Authors: V Agnello; S Ruddy; R J Winchester; C L Christian; H G Kunkel
Journal: Birth Defects Orig Artic Ser Date: 1975

7. C2 deficient systemic lupus erythematosus: its association with anti-Ro (SSA) antibodies.

Authors: P R Vandersteen; T T Provost; R E Jordon; F C McDuffie
Journal: Arch Dermatol Date: 1982-08

8. Urticarial vasculitis: report of a case and review of the literature.

Authors: W R Gammon; C E Wheeler
Journal: Arch Dermatol Date: 1979-01

9. Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.

Authors: A H Fielder; M J Walport; J R Batchelor; R I Rynes; C M Black; I A Dodi; G R Hughes
Journal: Br Med J (Clin Res Ed) Date: 1983-02-05

10. HLA antigen studies in a family with C2 deficiency.

Authors: G Opelz; M M Glovsky
Journal: J Immunogenet Date: 1976-10

12 in total

1. Defective prevention of immune precipitation in autoimmune diseases is independent of C4A*Q0.

Authors: G J Arason; R Kolka; A B Hreidarsson; H Gudjonsson; P M Schneider; L Fry; A Arnason
Journal: Clin Exp Immunol Date: 2005-06 Impact factor: 4.330

Review 2. Urticarial vasculitis and syndromes in association with connective tissue diseases.

Authors: R A Asherson; R Sontheimer
Journal: Ann Rheum Dis Date: 1991-11 Impact factor: 19.103

3. Recurrent infections, pericarditis and renal disease in a patient with total C2 deficiency and decreased NK cell function consistent with acute rheumatic fever and systemic lupus erythematosus.

Authors: D B Bittleman; K K Maves; J A Bertolatus; S M Bonsib; P Densen; Z K Ballas; J M Weiler
Journal: Ann Rheum Dis Date: 1994-04 Impact factor: 19.103

Lupus diseases associated with hereditary and acquired deficiencies of complement.

1. Cutaneous immunopathology: recent observations.

2. Heterogeneity of the clinical syndrome in patients with systemic lupus erythematosus and genetic deficiency of the second complement component.

3. Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies.

4. Characterization of a non-functional form of C1q found in patients with a genetically linked deficiency of C1q activity.

5. Homozygous C2 deficiency, lupus erythematosus, and anti-Ro (SSA) antibodies.

6. Hereditary C2 deficiency in systemic lupus erythematosus and acquired complement abnormalities in an unusual SLE-related syndrome.

7. C2 deficient systemic lupus erythematosus: its association with anti-Ro (SSA) antibodies.

8. Urticarial vasculitis: report of a case and review of the literature.

9. Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.

10. HLA antigen studies in a family with C2 deficiency.

1. Defective prevention of immune precipitation in autoimmune diseases is independent of C4A*Q0.

Review 2. Urticarial vasculitis and syndromes in association with connective tissue diseases.

3. Recurrent infections, pericarditis and renal disease in a patient with total C2 deficiency and decreased NK cell function consistent with acute rheumatic fever and systemic lupus erythematosus.

4. Hajdu-Cheney syndrome.

5. Uniparental isodisomy 6 associated with deficiency of the fourth component of complement.

6. C4A gene deletion and HLA associations in black Americans with systemic lupus erythematosus.

7. Association of C4B deficiency (C4B*Q0) with erythema nodosum in leprosy.

8. Acquired C1 inhibitor deficiency associated with systemic lupus erythematosus affecting the central nervous system.

Review 9. Monogenic systemic lupus erythematosus: insights in pathophysiology.

10. Antigen-induced B cell apoptosis is independent of complement C4.