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5. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system. Venneker GT; van Meegen M; de Kok-Nazaruk M; Hulsmans RF; de Waall LP; Bos JD; Asghar SS Exp Clin Immunogenet; 1996; 13(2):104-11. PubMed ID: 9063702 [TBL] [Abstract][Full Text] [Related]
6. [Familial Sjögren's syndrome, pseudolymphoma and selective C4 deficiency associated with cryoglobulinemia]. Batlle Fondrodona J; Cordero Sánchez M; Martínez López de Letona J; López Borrasca A Rev Clin Esp; 1980 Sep; 158(6):321-5. PubMed ID: 7209029 [No Abstract] [Full Text] [Related]
7. A shared cryoglobulin antigen in familial cryoglobulinemia. Nightingale SD; Pelley RP Am J Hum Genet; 1981 Sep; 33(5):722-34. PubMed ID: 6794362 [TBL] [Abstract][Full Text] [Related]
8. C4 polymorphism and HLA linkage: studies in a family with hereditary C4 deficiency. Ballow M; McLean RH; Yunis EJ; Awdeh ZL; O'Neill GJ; Einarson M; Alper CA Clin Immunol Immunopathol; 1981 Sep; 20(3):354-60. PubMed ID: 7341033 [No Abstract] [Full Text] [Related]
9. [IgG-IgM cryoglobulinemia with a purpura-arthralgia-nephritis syndrome]. Fontana A; Doll B; Joller H Schweiz Med Wochenschr; 1982 Jan; 112(1):7-13. PubMed ID: 7058315 [TBL] [Abstract][Full Text] [Related]
14. Renal involvement in essential mixed cryoglobulinemia. Perez GO; Pardo V; Fletcher M Am J Kidney Dis; 1987 Oct; 10(4):276-80. PubMed ID: 3310617 [TBL] [Abstract][Full Text] [Related]
15. Hereditary C4 deficiency--genetic studies and linkage to HLA. Ballow M; McLean RH; Einarson M; Martin S; Yunis EJ; Dupont B; O'Neill GJ Transplant Proc; 1979 Dec; 11(4):1710-2. PubMed ID: 531924 [No Abstract] [Full Text] [Related]
16. HLA typing of cultured amniotic cells for the prenatal diagnosis of complement C4 deficiency. Pollack MS; Ochs HD; Dupont B Clin Genet; 1980 Sep; 18(3):197-200. PubMed ID: 7438500 [No Abstract] [Full Text] [Related]
17. [Systemic lupus erythematosus in hereditary complement 4 deficiency]. Klein G; Tappeiner G; Hintner H; Scholz S; Wolff K Hautarzt; 1984 Jan; 35(1):27-32. PubMed ID: 6706571 [TBL] [Abstract][Full Text] [Related]
18. Relationship of tissue deposits of cryoglobulin to clinical features of mixed cryoglobulinemia. Feiner HD Hum Pathol; 1983 Aug; 14(8):710-5. PubMed ID: 6223875 [TBL] [Abstract][Full Text] [Related]
19. Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein. Donohoue PA; van Dop C; McLean RH; White PC; Jospe N; Migeon CJ J Clin Endocrinol Metab; 1986 May; 62(5):995-1002. PubMed ID: 3007562 [TBL] [Abstract][Full Text] [Related]
20. Molecular heterogeneity of second and fourth components of complement and their genes in systemic sclerosis and association of HLA alleles A1, B8 and DR3 with limited and DR5 with diffuse systemic sclerosis. Venneker GT; van den Hoogen FH; van Meegen M; de Kok-Nazaruk M; Hulsmans RF; Boerbooms AM; de Waal LP; Bos JD; Asghar SS Exp Clin Immunogenet; 1998; 15(2):90-9. PubMed ID: 9691203 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]