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Journal Abstract Search
268 related items for PubMed ID: 2237185
1. [Lupus and protein deficiencies of the classical complement pathway]. Weiss L, Maillet F, Kazatchkine M. Rev Prat; 1990 Sep 21; 40(21):1937-40. PubMed ID: 2237185 [Abstract] [Full Text] [Related]
2. Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4. Hartmann D, Fremeaux-Bacchi V, Weiss L, Meyer A, Blouin J, Hauptmann G, Kazatchkine M, Uring-Lambert B. J Clin Immunol; 1997 Mar 21; 17(2):176-84. PubMed ID: 9083894 [Abstract] [Full Text] [Related]
3. Which complement assays and typings are necessary for the diagnosis of complement deficiency in patients with lupus erythematosus? A study of 25 patients. Boeckler P, Meyer A, Uring-Lambert B, Goetz J, Cribier B, Hauptmann G, Lipsker D. Clin Immunol; 2006 Nov 21; 121(2):198-202. PubMed ID: 16987709 [Abstract] [Full Text] [Related]
5. Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE). Dragon-Durey MA, Rougier N, Clauvel JP, Caillat-Zucman S, Remy P, Guillevin L, Liote F, Blouin J, Ariey F, Lambert BU, Kazatchkine MD, Weiss L. Clin Exp Immunol; 2001 Jan 21; 123(1):133-9. PubMed ID: 11168010 [Abstract] [Full Text] [Related]
6. Relationship between the component and regulatory proteins of the classical pathway C3 convertase. Welch TR, Forristal J, Beischel L. J Lab Clin Med; 1986 Jun 21; 107(6):529-33. PubMed ID: 3635565 [Abstract] [Full Text] [Related]
7. Complete deficiencies of complement C4A and C4B including 2-bp insertion in codon 1213 are genetic risk factors of systemic lupus erythematosus in Thai populations. Ittiprasert W, Kantachuvesiri S, Pavasuthipaisit K, Verasertniyom O, Chaomthum L, Totemchokchyakarn K, Kitiyanant Y. J Autoimmun; 2005 Aug 21; 25(1):77-84. PubMed ID: 15998580 [Abstract] [Full Text] [Related]
15. 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 Sep 21; 13(2):104-11. PubMed ID: 9063702 [Abstract] [Full Text] [Related]
16. Partial C4 deficiency in two children with systemic lupus erythematosus. Bakkaloğlu A, Pascual M, Schifferli JA, Ozen S, Beşbaş N, Saatçi U. Turk J Pediatr; 1995 Sep 21; 37(2):147-51. PubMed ID: 7597765 [Abstract] [Full Text] [Related]
17. Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility. Fielder AH, Walport MJ, Batchelor JR, Rynes RI, Black CM, Dodi IA, Hughes GR. Br Med J (Clin Res Ed); 1983 Feb 05; 286(6363):425-8. PubMed ID: 6401549 [Abstract] [Full Text] [Related]