Barroso S, Rieubland C, Jose alvarez A, Lopez-Trascasa M, Bart P, Nunez-Roldan A
Immunology. 2006; 118(2):257-60.
PMID: 16771861
PMC: 1782290.
DOI: 10.1111/j.1365-2567.2006.02364.x.
Suankratay C, Mold C, Zhang Y, Potempa L, Lint T, Gewurz H
Clin Exp Immunol. 1998; 113(3):353-9.
PMID: 9737662
PMC: 1905066.
DOI: 10.1046/j.1365-2249.1998.00663.x.
Schifferli J, Morris S, Dash A, PETERS D
Clin Exp Immunol. 1981; 46(3):557-64.
PMID: 7337980
PMC: 1536306.
Zeitz H, Gewurz A, JONASSON O, Geis W, Gewurz H
Clin Exp Immunol. 1981; 46(2):420-4.
PMID: 7039890
PMC: 1536388.
Sakurai T, Fujita T, Kono I, Kabashima T, Yamane K, Tamura N
Clin Exp Immunol. 1982; 48(1):37-42.
PMID: 6979449
PMC: 1536587.
Determination of serum bactericidal activity with the aid of luminous bacteria.
Barak M, Ulitzur S, Merzbach D
J Clin Microbiol. 1983; 18(2):248-53.
PMID: 6619281
PMC: 270786.
DOI: 10.1128/jcm.18.2.248-253.1983.
Inherited deficiency of C8 in a patient with recurrent meningococcal infections: further evidence for a dysfunctional C8 molecule and nonlinkage to the HLA system.
Densen P, Brown E, ONEILL G, Tedesco F, Clark R, Frank M
J Clin Immunol. 1983; 3(1):90-9.
PMID: 6186685
DOI: 10.1007/BF00919144.
Terminal complement component deficiencies and rheumatic disease: development of a rheumatic syndrome and anticomplementary activity in a patient with complete C6 deficiency.
Wisnieski J, Naff G, Pensky J, Sorin S
Ann Rheum Dis. 1985; 44(10):716-22.
PMID: 3931570
PMC: 1001750.
DOI: 10.1136/ard.44.10.716.
Inherited C8 beta subunit deficiency in a patient with recurrent meningococcal infections: in vivo functional kinetic analysis of C8.
Rao C, Minta J, Laski B, Alper C, Gelfand E
Clin Exp Immunol. 1985; 60(1):183-90.
PMID: 3924449
PMC: 1577010.
SLE-like and sicca symptoms in late component (C9) complement deficiency.
Sugimoto M, Nishikai M, Sato A, Suzuki Y, Nihei M, Uchida J
Ann Rheum Dis. 1987; 46(2):153-5.
PMID: 3827337
PMC: 1002082.
DOI: 10.1136/ard.46.2.153.
Lupus diseases associated with hereditary and acquired deficiencies of complement.
Agnello V
Springer Semin Immunopathol. 1986; 9(2-3):161-78.
PMID: 3544278
DOI: 10.1007/BF02099020.
C7 deficiency and persistent haematuria.
Sakano T, Hamasaki T, Mori M, Ohta T, Ueda K, Ishigame K
Eur J Pediatr. 1988; 147(5):516-7.
PMID: 3409927
DOI: 10.1007/BF00441978.
Formation of soluble immune complexes by complement in sera of patients with various hypocomplementemic states. Difference between inhibition of immune precipitation and solubilization.
Schifferli J, Steiger G, Hauptmann G, Spaeth P, Sjoholm A
J Clin Invest. 1985; 76(6):2127-33.
PMID: 2934406
PMC: 424324.
DOI: 10.1172/JCI112217.
Familial deficiency of the seventh component of complement associated with recurrent meningococcal infections.
Nurnberger W, Pietsch H, Seger R, Bufon T, Wahn V
Eur J Pediatr. 1989; 148(8):758-60.
PMID: 2792129
DOI: 10.1007/BF00443104.
Functionally active complement proteins C6 and C7 detected in C6- and C7-deficient individuals.
Wurzner R, Orren A, Potter P, Morgan B, Ponard D, Spath P
Clin Exp Immunol. 1991; 83(3):430-7.
PMID: 2004484
PMC: 1535307.
DOI: 10.1111/j.1365-2249.1991.tb05656.x.
Combined total deficiency of C7 and C4B with systemic lupus erythematosus (SLE).
Segurado O, Iglesias-Casarrubios P, Martinez-Laso J, Vicario J, Fontan G, Lopez-Trascasa M
Clin Exp Immunol. 1992; 87(3):410-4.
PMID: 1347491
PMC: 1554335.
DOI: 10.1111/j.1365-2249.1992.tb03011.x.
