Similar articles for PMID: 21654842

Year	Number of Results
1982	1
1987	1
1989	2
1993	2
1994	1
1996	2
1997	4
1998	2
2000	4
2001	1
2002	1
2004	3
2005	1
2006	4
2007	5
2008	4
2009	4
2010	8
2011	6
2012	4
2013	3
2014	2
2015	4
2017	2
2018	2
2019	3
2022	1
2024	0

1

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. Schejbel L, et al. Genes Immun. 2011 Dec;12(8):626-34. doi: 10.1038/gene.2011.39. Epub 2011 Jun 9. Genes Immun. 2011. PMID: 21654842

2

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. Sun-Tan C, et al. Turk J Pediatr. 2010 Mar-Apr;52(2):184-6. Turk J Pediatr. 2010. PMID: 20560256

3

Molecular basis of hereditary C1q deficiency.

Petry F. Petry F. Immunobiology. 1998 Aug;199(2):286-94. doi: 10.1016/S0171-2985(98)80033-8. Immunobiology. 1998. PMID: 9777412 Review.

4

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. Gulez N, et al. J Investig Allergol Clin Immunol. 2010;20(3):255-8. J Investig Allergol Clin Immunol. 2010. PMID: 20635792 Free article.

5

Hereditary C1q deficiency and systemic lupus erythematosus.

Bowness P, Davies KA, Norsworthy PJ, Athanassiou P, Taylor-Wiedeman J, Borysiewicz LK, Meyer PA, Walport MJ. Bowness P, et al. QJM. 1994 Aug;87(8):455-64. QJM. 1994. PMID: 7922299 Review.

6

Clinical variability and characteristic autoantibody profile in primary C1q complement deficiency.

Vassallo G, Newton RW, Chieng SE, Haeney MR, Shabani A, Arkwright PD. Vassallo G, et al. Rheumatology (Oxford). 2007 Oct;46(10):1612-4. doi: 10.1093/rheumatology/kem207. Rheumatology (Oxford). 2007. PMID: 17890276

7

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. Jlajla H, et al. Immunobiology. 2014 Mar;219(3):241-6. doi: 10.1016/j.imbio.2013.10.010. Epub 2013 Nov 6. Immunobiology. 2014. PMID: 24331529 Review.

8

Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey.

Berkel AI, Birben E, Oner C, Oner R, Loos M, Petry F. Berkel AI, et al. Immunobiology. 2000 Jan;201(3-4):347-55. doi: 10.1016/S0171-2985(00)80089-3. Immunobiology. 2000. PMID: 10776791

9

Deficiency of the first component of human complement.

Reid KB. Reid KB. Immunodefic Rev. 1989;1(3):247-60. Immunodefic Rev. 1989. PMID: 2561058 Review.

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. van Schaarenburg RA, et al. Immunobiology. 2015 Mar;220(3):422-7. doi: 10.1016/j.imbio.2014.10.005. Epub 2014 Oct 18. Immunobiology. 2015. PMID: 25454803

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