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.
107 related articles for article (PubMed ID: 10776791)
1. Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey. Berkel AI; Birben E; Oner C; Oner R; Loos M; Petry F Immunobiology; 2000 Jan; 201(3-4):347-55. PubMed ID: 10776791 [TBL] [Abstract][Full Text] [Related]
2. Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis. Petry F; Berkel AI; Loos M Hum Genet; 1997 Jul; 100(1):51-6. PubMed ID: 9225968 [TBL] [Abstract][Full Text] [Related]
3. Hereditary C1q deficiency: a new family with C1qA deficiency. Sun-Tan C; Ozgür TT; Kilinç G; Topaloğlu R; Gököz O; Ersoy-Evans S; Sanal O Turk J Pediatr; 2010; 52(2):184-6. PubMed ID: 20560256 [TBL] [Abstract][Full Text] [Related]
5. Homozygosity for a novel mutation in the C1q C chain gene in a Turkish family with hereditary C1q deficiency. Gulez N; Genel F; Atlihan F; Gullstrand B; Skattum L; Schejbel L; Garred P; Truedsson L J Investig Allergol Clin Immunol; 2010; 20(3):255-8. PubMed ID: 20635792 [TBL] [Abstract][Full Text] [Related]
6. Molecular basis of hereditary C1q deficiency. Petry F Immunobiology; 1998 Aug; 199(2):286-94. PubMed ID: 9777412 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family. Topaloglu R; Bakkaloglu A; Slingsby JH; Mihatsch MJ; Pascual M; Norsworthy P; Morley BJ; Saatci U; Schifferli JA; Walport MJ Kidney Int; 1996 Aug; 50(2):635-42. PubMed ID: 8840296 [TBL] [Abstract][Full Text] [Related]
9. New C1q mutation in a Tunisian family. Jlajla H; Sellami MK; Sfar I; Laadhar L; Zerzeri Y; Abdelmoula MS; Gorgi Y; Dridi MF; Makni S Immunobiology; 2014 Mar; 219(3):241-6. PubMed ID: 24331529 [TBL] [Abstract][Full Text] [Related]
10. Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infections. van Schaarenburg RA; Daha NA; Schonkeren JJ; Nivine Levarht EW; van Gijlswijk-Janssen DJ; Kurreeman FA; Roos A; van Kooten C; Koelman CA; Ernst-Kruis MR; Toes RE; Huizinga TW; Lankester AC; Trouw LA Immunobiology; 2015 Mar; 220(3):422-7. PubMed ID: 25454803 [TBL] [Abstract][Full Text] [Related]
11. Identification of novel coding mutation in C1qA gene in an African-American pedigree with lupus and C1q deficiency. Namjou B; Keddache M; Fletcher D; Dillon S; Kottyan L; Wiley G; Gaffney PM; Wakeland BE; Liang C; Wakeland EK; Scofield RH; Kaufman K; Harley JB Lupus; 2012 Sep; 21(10):1113-8. PubMed ID: 22472776 [TBL] [Abstract][Full Text] [Related]
12. Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutations. Schejbel L; Skattum L; Hagelberg S; Åhlin A; Schiller B; Berg S; Genel F; Truedsson L; Garred P Genes Immun; 2011 Dec; 12(8):626-34. PubMed ID: 21654842 [TBL] [Abstract][Full Text] [Related]
13. Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families. Slingsby JH; Norsworthy P; Pearce G; Vaishnaw AK; Issler H; Morley BJ; Walport MJ Arthritis Rheum; 1996 Apr; 39(4):663-70. PubMed ID: 8630118 [TBL] [Abstract][Full Text] [Related]
14. Analysis of C1q polymorphisms suggests association with systemic lupus erythematosus, serum C1q and CH50 levels and disease severity. Martens HA; Zuurman MW; de Lange AH; Nolte IM; van der Steege G; Navis GJ; Kallenberg CG; Seelen MA; Bijl M Ann Rheum Dis; 2009 May; 68(5):715-20. PubMed ID: 18504288 [TBL] [Abstract][Full Text] [Related]
15. Common silent mutations in all types of hereditary complement C1q deficiencies. Petry F; Loos M Immunogenetics; 2005 Sep; 57(8):566-71. PubMed ID: 16086173 [TBL] [Abstract][Full Text] [Related]
17. Family study of natural killer cell activity in C1q-deficient patients with systemic lupus erythematosus-like syndrome: association between impaired natural killer cell function and C1q deficiency. Tóth J; Starsia Z; Buc M; Stefanovic J Immunobiology; 1989 Nov; 180(1):47-54. PubMed ID: 2625354 [TBL] [Abstract][Full Text] [Related]
18. C1q deficiency in an Inuit family: identification of a new class of C1q disease-causing mutations. Marquart HV; Schejbel L; Sjoholm A; Martensson U; Nielsen S; Koch A; Svejgaard A; Garred P Clin Immunol; 2007 Jul; 124(1):33-40. PubMed ID: 17513176 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]