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Scholar Results 1 - 10 of about 101 related to FRIEND: Deficiency of the second component of complement (C2) with chronic vasculitis. (0.10 sec) 

Deficiency of the second component of complement (C2) with chronic vasculitis


P FRIEND, JE REPINE, Y KIM, CC Clawson, … - Annals of Internal …, 1975 - Am Coll Physicians
A patient had complete deficiency of the second component of complement associated with chronic
vasculitis and increased susceptibility to infection. We discuss here results of the complement
profile, histocompatibility typing, ...
Cited by 37 - Related articles - All 3 versions

Selective deficiency of the second component of complement in a patient with …


EW Gelfand, JE Clarkson, JO Minta - Clinical Immunology and …, 1975 - Elsevier
The serum hemolytic complement activity of a patient with a 4-yr history of anaphylactoid purpura
was markedly decreased. This abnormality was due to a selective deficiency of the second component
of complement (C2). ...
Cited by 54 - Related articles - All 2 versions

Inherited C2 deficiency and systemic lupus erythematosus: studies on a family


CK Osterland, L Espinoza, LP Parker, PH … - Annals of Internal …, 1975 - Am Coll Physicians
A patient is described in which an inherited defect in the synthesis of C2 complement component
coexisted with the disease systemic lupus erythematosus. The family studies show evidence of the
autosomal recessive nature of the ...
Cited by 48 - Related articles - All 2 versions

Deficiency of the second component of complement associated with anaphylactoid …

- nih.gov [PDF] 
M Sussman, JH Jones, JD Almeida, PJ … - Clinical and …, 1973 - pubmedcentral.nih.gov
Deficiency of the second component of complement (C2) has been described in five families
(Silverstein, 1960; Klemperer, Woodworth, Rosen & Austen, 1966; Klemperer, Austen & Rosen, 1967;
Cooper, Ten Bensel & Kohler, 1968; ...
Cited by 74 - Related articles - All 2 versions

Hereditary complement (C2) deficiency with dermatomyositis.


JP Leddy, RC Griggs, MR Klemperer, MM … - The American journal of …, 1975 - ncbi.nlm.nih.gov
A 60 year old white man in previous good health presented with a 6 month history of progressive
muscle weakness. Clinical and laboratory findings were typical of dermatomyositis. Muscle biopsy
confirmed the presence of inflammatory myopathy; deposits of immunoglobulin G (IgG), ...
Cited by 64 - Related articles

[CITATION] Lupus érythémateux aigus et déficits héréditaires en complément. A propos d'un …


G Hauptmann, E Grosshans, E Heid - Ann Derm Syph (Paris), 1974
Cited by 60 - Related articles

C2 Deficiency DEVELOPMENT OF LUPUS ERYTHEMATOSUS

- nih.gov [PDF] 
NK Day, H Geiger, R McLean, A Michael … - Journal of Clinical …, 1973 - pubmedcentral.nih.gov
A BSTRACT The study of serum from a patient with C2 deficiency is described. The patient had an
episode of pneumococcal meningitis at 5 mo of age with seizures and transient hemiparesis and
apparent purpuric skin lesions. He ...
Cited by 74 - Related articles - All 5 versions

Recurrent pyogenic infections in individuals with absence of the second …


HA Sampson, AM Walchner, PJ Baker - Journal of Clinical Immunology, 1982 - Springer
While deficiency of the terminal components of comple- ment (C3-C8) has classically been associated
with recur- rent pyogenic infections, it has become apparent that C2 deficiency is also associated
with recurrent infections in some ...
Cited by 20 - Related articles - All 3 versions

Hereditary C2 deficiency: diagnosis and HLA gene complex associations


DJ Gibson, D Glass, CB Carpenter, PH … - The Journal of …, 1976 - Am Assoc Immnol
Nine families with genetically controlled C2 deficiency have been described where the propositii and
family members are heterozygous C2 deficient. The diagnosis of hereditary C2 heterozygous deficiency
was suspected on the basis of ...
Cited by 37 - Related articles - All 2 versions

C2 deficiency in man. Genetic relationship to a mixed lymphocyte reaction …


PS Friend, BS Handwerger, Y Kim, AF Michael, EJ … - Immunogenetics, 1975 - Springer
Abstract. Three unrelated individuals with, respectively, lupus erythematosus, polyarteritis, and
membranoproliferative glomerulonephritis and totally deficient in the second component of comple-
ment are demonstrated to be ...
Cited by 23 - Related articles


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