| scholarly article | Q13442814 |
| P2093 | author name string | R. A. Good | |
| Michael AF Jr | |||
| H. Gewurz | |||
| A. F. Michael | |||
| R. J. Pickering | |||
| R. C. Herdman | |||
| P2860 | cites work | Immunochemical quantitation of antigens by single radial immunodiffusion | Q28248574 |
| Clinical studies of hemolytic complement and the 11S component | Q33475391 | ||
| SERUM LEVELS OF BETA-1C GLOBULIN, A COMPLEMENT COMPONENT, IN THE NEPHRITIDES, LIPOID NEPHROSIS, AND OTHER CONDITIONS. | Q35568973 | ||
| IMMUNOLOGICAL STUDIES OF THE 11S PROTEIN COMPONENT OF THE HUMAN COMPLEMENT SYSTEM | Q36266959 | ||
| Interactions of the complement system with endotoxic lipopolysaccharide: consumption of each of the six terminal complement components | Q36269413 | ||
| Deficiency of C1r in human serum. Effects on the structure and function of macromolecular C1. | Q36270181 | ||
| Passive hemolysis by serum and cobra venom factor: a new mechanism inducing membrane damage by complement | Q37423457 | ||
| Experimental glomerulonephritis: immunological events and pathogenetic mechanisms | Q39964244 | ||
| Acute poststreptococcal glomerulonephritis: immune deposit disease | Q40328050 | ||
| Hereditary deficiency of the second component of complement (C'2) in man. | Q40328442 | ||
| Isolation and characterization of two beta1-glycoproteins of human serum | Q41943613 | ||
| Chronic glomerulonephritis associated with low serum complement activity (chronic hypocomplementemic glomerulonephritis) | Q45031766 | ||
| Inherited c'2 deficiency in man: lack of immunochemically detectable c'2 protein in serums from deficient individuals | Q47891267 | ||
| Diffuse glomerulonephritis associated with infected ventriculoatrial shunt. | Q54394894 | ||
| Methods for the separation, purification and measurement of nine components of hemolytic complement in guinea-pig serum | Q56591964 | ||
| Complement-dependent biological functions in complement deficiency in man | Q70066850 | ||
| THE BETA-1C GLOBULIN IN CHILDHOOD NEPHROTIC SYNDROME: LABORATORY DIAGNOSIS OF PROGRESSIVE GLOMERULONEPHRITIS | Q78478920 | ||
| The complement profile in acute glomerulonephritis systemic lupus erythematosus and hypocomplementemic chronic glomerulonephritis. Contrasts and experimental correlations | Q93698055 | ||
| Inherited C'2 deficiency in man. Lack of immunochemically detectable C'2 protein in serums from deficient individuals | Q95784804 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | glomerulonephritis | Q605006 |
| P304 | page(s) | 30-43 | |
| P577 | publication date | 1971-01-01 | |
| P1433 | published in | The Journal of Pediatrics | Q7743611 |
| P1476 | title | The complement system in chronic glomerulonephritis: Three newly associated aberrations | |
| P478 | volume | 78 |
| Q40344883 | An association between C1 esterase inhibitor deficiency and lupus erythematosus: report of two cases and review of the literature |
| Q93856155 | An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritis |
| Q70086721 | Atypical hypocomplementemic vasculitis syndrome in a child |
| Q34506917 | C2 deficiency. Development of lupus erythematosus |
| Q40898367 | Complement and glomerulonephritis--an update |
| Q67462750 | Complement and host defense against infection |
| Q70775616 | Complement phenotypes in glomerulonephritis: increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura |
| Q40280819 | Cutaneous infections and disorders of inflammation |
| Q93748043 | Deficiency of the second component of complement associated with anaphylactoid purpura and presence of mycoplasma in the serum |
| Q72939638 | Detection and analysis of inborn and acquired complement abnormalities |
| Q71746824 | Deviations in the complement system and chronic glomerulonephritis |
| Q40130196 | Disease States in Genetic Complement Deficiencies |
| Q45049211 | Extramembranous glomerulonephritis in childhood: Relationship to systemic lupus erythematosus |
| Q24302896 | Familial deficiency of two subunits of the first component of complement. C1r and C1s associated with a lupus erythematosus-like disease |
| Q44749349 | Genetic Independence between the HL‐A System and Deficits in the First and Sixth Components of Complement |
| Q39605266 | Genetics of complement deficiencies associated with lupus-like syndromes |
| Q24514917 | Genetics of the complement system |
| Q69375411 | Glomerulonephritis in childhood |
| Q40887620 | Hereditary C2 deficiency and systemic lupus erythematosus associated with severe glomerulonephritis |
| Q41194798 | Hereditary angio-oedema with mesangiocapillary glomerulonephritis |
| Q33837865 | Hereditary angioedema and thyroid autoimmunity |
| Q54775450 | Hereditary angioedema and “familial” lupus erythematosus in identical twin boys |
| Q43411867 | Hereditary complement (C2) deficiency with dermatomyositis |
| Q40158603 | Heterogeneity of the clinical syndrome in patients with systemic lupus erythematosus and genetic deficiency of the second complement component |
| Q40855806 | Homozygous C2 deficiency with fulminant lupus erythematosus. severe nephritis via the alternative complement pathway |
| Q70762044 | Hypocomplementemic idiopathic membranous glomerulopathy |
| Q39869252 | Hypomorphic variant of C3, arthritis, and chronic glomerulonephritis |
| Q53769947 | Immunity deficiency in pathogenesis of glomerulonephritis. |
| Q40932039 | Immunopathology of membranoproliferative glomerulonephritis with subendothelial deposits (Type I MPGN) |
| Q41676564 | Inborn Clr deficiency with a mild lupus-like syndrome |
| Q71172970 | Inherited complement component deficiencies in membranoproliferative glomerulonephritis |
| Q40118356 | Inherited deficiencies of complement proteins in man |
| Q40138807 | Inherited disorders of complement |
| Q68139403 | Long-term follow-up of non-systemic lupus erythematosus glomerulonephritis in patients with hereditary angioedema: report of four cases |
| Q39756275 | Lupus diseases associated with hereditary and acquired deficiencies of complement |
| Q37951577 | Membranous nephropathy in childhood and its treatment |
| Q70000316 | Mesangiocapillary nephritis, partial lipodystrophy, and hypocomplementaemia |
| Q33478578 | Partial H (beta 1H) deficiency and glomerulonephritis in two families |
| Q39776393 | Pathogenesis and approaches to therapy of membranoproliferative glomerulonephritis |
| Q45215996 | Pathogenesis and treatment of membranous nephropathy |
| Q48028867 | Pathways of complement activation in glomerulonephritis |
| Q47791028 | Prevalence of autoantibodies in a group of hereditary angioedema patients |
| Q41958527 | Reticulate erythema—a prodrome in hereditary angio-oedema |
| Q46173002 | Selective deficiency of the second component of complement in a patient with anaphylactoid purpura |
| Q70033141 | Skin lesions, angio-oedema, and hypocomplementaemia |
| Q47978861 | Spontaneous chemotaxis in patients with glomerulonephritis and the nephrotic syndrome |
| Q39848257 | The associations and relationships of congenital immune deficiency states and autoimmune phenomena |
| Q44038430 | The effect of anticomplementary substances on properdin in normal and C2-deficient sera |
| Q35144909 | The immunological basis of glomerulonephritis. |
| Q40894160 | The role of complement, immunoglobulin and bacterial antigen in coagulase-negative staphylococcal shunt nephritis |
| Q71777938 | [Hereditary deficiency of C1 esterase inhibitor. Lupus and glomerulonephritis] |
Search more.