These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
141 related articles for article (PubMed ID: 8630118)
21. C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma. Topaloglu R; Taskiran EZ; Tan C; Erman B; Ozaltin F; Sanal O Clin Rheumatol; 2012 Jul; 31(7):1123-6. PubMed ID: 22576477 [TBL] [Abstract][Full Text] [Related]
22. Development of systemic lupus erythematosus in a patient with selective complete C1q deficiency. Berkel AI; Petry F; Sanal O; Tinaztepe K; Ersoy F; Bakkaloglu A; Loos M Eur J Pediatr; 1997 Feb; 156(2):113-5. PubMed ID: 9039514 [TBL] [Abstract][Full Text] [Related]
23. PCR-RFLP genotyping of C1q mutations and single nucleotide polymorphisms in Malaysian patients with systemic lupus erythematosus. Chew CH; Chua KH; Lian LH; Puah SM; Tan SY Hum Biol; 2008 Feb; 80(1):83-93. PubMed ID: 18505047 [TBL] [Abstract][Full Text] [Related]
25. Monogenic interferonopathies: Phenotypic and genotypic findings of CANDLE syndrome and its overlap with C1q deficient SLE. Al-Mayouf SM; AlSaleem A; AlMutairi N; AlSonbul A; Alzaid T; Alazami AM; Al-Mousa H Int J Rheum Dis; 2018 Jan; 21(1):208-213. PubMed ID: 29115062 [TBL] [Abstract][Full Text] [Related]
26. The molecular basis of complete complement C4A and C4B deficiencies in a systemic lupus erythematosus patient with homozygous C4A and C4B mutant genes. Rupert KL; Moulds JM; Yang Y; Arnett FC; Warren RW; Reveille JD; Myones BL; Blanchong CA; Yu CY J Immunol; 2002 Aug; 169(3):1570-8. PubMed ID: 12133986 [TBL] [Abstract][Full Text] [Related]
27. A patient with hereditary C1q deficiency. Ozsoylu S Turk J Pediatr; 2010; 52(6):674; author reply 674. PubMed ID: 21428208 [No Abstract] [Full Text] [Related]
28. Pediatric systemic lupus erythematosus with C1q deficiency. Kallel-Sellami M; Baili-Klila L; Zerzeri Y; Laadhar L; Blouin J; Abdelmoula MS; Zitouni M; Fremeaux-Bacchi V; Ben Dridi MF; Makni S Ann N Y Acad Sci; 2007 Jun; 1108():193-6. PubMed ID: 17893985 [TBL] [Abstract][Full Text] [Related]
29. Homozygous single nucleotide polymorphism of the complement C1QA gene is associated with decreased levels of C1q in patients with subacute cutaneous lupus erythematosus. Racila DM; Sontheimer CJ; Sheffield A; Wisnieski JJ; Racila E; Sontheimer RD Lupus; 2003; 12(2):124-32. PubMed ID: 12630757 [TBL] [Abstract][Full Text] [Related]
30. Systemic lupus erythematosus with C1q deficiency. Stone NM; Williams A; Wilkinson JD; Bird G Br J Dermatol; 2000 Mar; 142(3):521-4. PubMed ID: 10735963 [TBL] [Abstract][Full Text] [Related]
31. Clinical presentation of human C1q deficiency: How much of a lupus? Stegert M; Bock M; Trendelenburg M Mol Immunol; 2015 Sep; 67(1):3-11. PubMed ID: 25846716 [TBL] [Abstract][Full Text] [Related]
32. 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; 25(1):77-84. PubMed ID: 15998580 [TBL] [Abstract][Full Text] [Related]
33. Clinical presentations and molecular basis of complement C1r deficiency in a male African-American patient with systemic lupus erythematosus. Wu YL; Brookshire BP; Verani RR; Arnett FC; Yu CY Lupus; 2011 Oct; 20(11):1126-34. PubMed ID: 21784777 [TBL] [Abstract][Full Text] [Related]
34. C1q knock-out mice for the study of complement deficiency in autoimmune disease. Botto M Exp Clin Immunogenet; 1998; 15(4):231-4. PubMed ID: 10072632 [TBL] [Abstract][Full Text] [Related]
35. Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency. van Schaarenburg RA; Schejbel L; Truedsson L; Topaloglu R; Al-Mayouf SM; Riordan A; Simon A; Kallel-Sellami M; Arkwright PD; Åhlin A; Hagelberg S; Nielsen S; Shayesteh A; Morales A; Tam S; Genel F; Berg S; Ketel AG; Merlijn van den Berg J; Kuijpers TW; Olsson RF; Huizinga TW; Lankester AC; Trouw LA J Autoimmun; 2015 Aug; 62():39-44. PubMed ID: 26119135 [TBL] [Abstract][Full Text] [Related]
36. Systemic lupus erythematosus due to C1q deficiency with progressive encephalopathy, intracranial calcification and acquired moyamoya cerebral vasculopathy. Troedson C; Wong M; Dalby-Payne J; Wilson M; Dexter M; Rice GI; Crow YJ; Dale RC Lupus; 2013 May; 22(6):639-43. PubMed ID: 23651859 [TBL] [Abstract][Full Text] [Related]
37. Hereditary complement deficiency and lupus: report of four Tunisian cases. Kallel-Sellami M; Baili-Klila L; Zerzeri Y; Laadhar L; Blouin J; Abdelmalek R; Fremeaux-Bacchi V; Zitouni M; Makni S Ann N Y Acad Sci; 2007 Jun; 1108():197-202. PubMed ID: 17893986 [TBL] [Abstract][Full Text] [Related]
38. Association Between C1q, TRAIL, and Tim-1 Gene Polymorphisms and Systemic Lupus Erythematosus. Yu Y; Zhu C; Zhou S; Chi S Genet Test Mol Biomarkers; 2018 Sep; 22(9):546-553. PubMed ID: 30183357 [TBL] [Abstract][Full Text] [Related]
39. Molecular defects of the C7 gene in two patients with complement C7 deficiency. Barroso S; Rieubland C; José álvarez A; López-Trascasa M; Bart PA; Núñez-Roldán A; Sánchez B Immunology; 2006 Jun; 118(2):257-60. PubMed ID: 16771861 [TBL] [Abstract][Full Text] [Related]
40. [Structure and function of complement protein C1q and its role in the development of autoimmune diseases]. Smykał-Jankowiak K; Niemir ZI Postepy Hig Med Dosw (Online); 2009 Apr; 63():134-41. PubMed ID: 19373194 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]