Truedsson L - Search Results

1

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. Among authors: truedsson l. J Investig Allergol Clin Immunol. 2010;20(3):255-8. J Investig Allergol Clin Immunol. 2010. PMID: 20635792 Free article.

2

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. Among authors: truedsson l. Genes Immun. 2011 Dec;12(8):626-34. doi: 10.1038/gene.2011.39. Epub 2011 Jun 9. Genes Immun. 2011. PMID: 21654842

3

Properdin deficiency in a boy with fulminant meningococcal septic shock.

Genel F, Atlihan F, Gulez N, Sjöholm AG, Skattum L, Truedsson L. Genel F, et al. Among authors: truedsson l. Acta Paediatr. 2006 Nov;95(11):1498-1500. doi: 10.1080/08035250600603008. Acta Paediatr. 2006. PMID: 17062484

4

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. van Schaarenburg RA, et al. Among authors: truedsson l. J Autoimmun. 2015 Aug;62:39-44. doi: 10.1016/j.jaut.2015.06.002. Epub 2015 Jun 26. J Autoimmun. 2015. PMID: 26119135

5

Inherited Classical and Alternative Pathway Complement Deficiencies in Children: A Single Center Experience.

Genel F, Erdem SB, Gülez N, Karaman S, Nacaroglu HT, Skattum L, Truedsson L. Genel F, et al. Among authors: truedsson l. Iran J Immunol. 2018 Dec;15(4):309-320. doi: 10.22034/IJI.2018.39400. Iran J Immunol. 2018. PMID: 30593745 Free article.

6

Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis.

Genel F, Sjöholm AG, Skattum L, Truedsson L. Genel F, et al. Among authors: truedsson l. Scand J Infect Dis. 2005;37(8):615-618. doi: 10.1080/00365540510034536. Scand J Infect Dis. 2005. PMID: 16138437

7

Molecular characterization of two novel cases of complete complement inhibitor Factor I deficiency.

Nita IM, Genel F, Nilsson SC, Smart J, Truedsson L, Choo S, Blom AM. Nita IM, et al. Among authors: truedsson l. Mol Immunol. 2011 Apr;48(8):1068-72. doi: 10.1016/j.molimm.2011.01.012. Epub 2011 Feb 12. Mol Immunol. 2011. PMID: 21316765 Free article.

8

Complement deficiency states and associated infections.

Skattum L, van Deuren M, van der Poll T, Truedsson L. Skattum L, et al. Among authors: truedsson l. Mol Immunol. 2011 Aug;48(14):1643-55. doi: 10.1016/j.molimm.2011.05.001. Epub 2011 May 31. Mol Immunol. 2011. PMID: 21624663 Review.

9

Analysis of Anti-C1q Autoantibodies by Western Blot.

Verlemyr A, Truedsson L, Skattum L. Verlemyr A, et al. Among authors: truedsson l. Methods Mol Biol. 2019;1901:183-189. doi: 10.1007/978-1-4939-8949-2_14. Methods Mol Biol. 2019. PMID: 30539577

10

Binding of immune complexes to erythrocyte CR1 (CD35): difference in requirement of classical pathway components and indication of alternative pathway-mediated binding in C2-deficiency.

Klint C, Gullstrand B, Sturfelt G, Truedsson L. Klint C, et al. Among authors: truedsson l. Scand J Immunol. 2000 Jul;52(1):103-8. doi: 10.1046/j.1365-3083.2000.00752.x. Scand J Immunol. 2000. PMID: 10886790 Free article.

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