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31. [Double C2 and C7 deficiency in the same subject: study of complement and HL-A system]. Lehner-Netsch G; Simard J; Prochazka E; Brun G; Delage JM Union Med Can; 1978 Oct; 107(10):928-32. PubMed ID: 705955 [No Abstract] [Full Text] [Related]
32. Inherited deficiency of the third component of complement associated with recurrent pyogenic infections, circulating immune complexes, and vasculitis in a Dutch family. Roord JJ; Daha M; Kuis W; Verbrugh HA; Verhoef J; Zegers BJ; Stoop JW Pediatrics; 1983 Jan; 71(1):81-7. PubMed ID: 6848983 [TBL] [Abstract][Full Text] [Related]
33. Serum complement C2 levels in patients suffering from cystic fibrosis (CF). László A; Füst G; Pánya A; Gyurkovits K Acta Paediatr Hung; 1988-1989; 29(3-4):289-92. PubMed ID: 3269267 [TBL] [Abstract][Full Text] [Related]
34. Prevalence of the type I complement C2 deficiency gene in Swedish systemic lupus erythematosus patients. Truedsson L; Sturfelt G; Nived O Lupus; 1993 Oct; 2(5):325-7. PubMed ID: 8305927 [TBL] [Abstract][Full Text] [Related]
35. Hereditary C2 deficiency: Genetic studies and association with the HL-A system. Day NK; L'Esperance R; Good RA; Michael AF; Hansen JA; Dupont B; Jersild C J Exp Med; 1975 Jun; 141(6):1464-9. PubMed ID: 1127385 [TBL] [Abstract][Full Text] [Related]
36. Hereditary deficiency of C2 in association with linear scleroderma 'en coup de sabre'. Hulsmans RF; Asghar SS; Siddiqui AH; Cormane RH Arch Dermatol; 1986 Jan; 122(1):76-9. PubMed ID: 3942410 [TBL] [Abstract][Full Text] [Related]
37. [Hypocomplementemia resulting from heterozygous C2 deficiency, polyarthritis and urticaria - comparison to Mac Duffie's syndrome]. Peltier AP; Vial MC; Kuntz D; Allegre P Nouv Presse Med; 1980 Feb; 9(6):382-3. PubMed ID: 7383911 [No Abstract] [Full Text] [Related]
38. Complementing the patient: a complement component deficiency in a patient with recurrent infections and glomerulonephritis. Sinclair D; Wilde G; Bex S; Peters S Clin Lab; 2005; 51(9-10):505-7. PubMed ID: 16285472 [TBL] [Abstract][Full Text] [Related]
39. Complement factor 2 deficiency: a clinical and serological family study. D'Cruz D; Taylor J; Ahmed T; Asherson R; Khamashta M; Hughes GR Ann Rheum Dis; 1992 Nov; 51(11):1254-6. PubMed ID: 1361318 [TBL] [Abstract][Full Text] [Related]
40. Major histocompatibility complex genes in a Mexican family with deficiency of the second component of the complement system. Melín-Aldana H; Reyes P; Vargas-Alarcón G; Yamamoto-Furusho JK; Granados J Rev Invest Clin; 1996; 48(4):307-9. PubMed ID: 8966394 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]