Genel F - Search Results

1

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. Scand J Infect Dis. 2005;37(8):615-618. doi: 10.1080/00365540510034536. Scand J Infect Dis. 2005. PMID: 16138437

2

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. Acta Paediatr. 2006 Nov;95(11):1498-1500. doi: 10.1080/08035250600603008. Acta Paediatr. 2006. PMID: 17062484

3

Genetic, molecular and functional analyses of complement factor I deficiency.

Nilsson SC, Trouw LA, Renault N, Miteva MA, Genel F, Zelazko M, Marquart H, Muller K, Sjöholm AG, Truedsson L, Villoutreix BO, Blom AM. Nilsson SC, et al. Among authors: genel f. Eur J Immunol. 2009 Jan;39(1):310-23. doi: 10.1002/eji.200838702. Eur J Immunol. 2009. PMID: 19065647 Free article.

4

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: genel f. 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.

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

6

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

7

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. Iran J Immunol. 2018 Dec;15(4):309-320. doi: 10.22034/IJI.2018.39400. Iran J Immunol. 2018. PMID: 30593745 Free article.

8

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: genel f. J Autoimmun. 2015 Aug;62:39-44. doi: 10.1016/j.jaut.2015.06.002. Epub 2015 Jun 26. J Autoimmun. 2015. PMID: 26119135

9

IgA and/or IgG subclass deficiency in children with recurrent respiratory infections and its relationship with chronic pulmonary damage.

Ozkan H, Atlihan F, Genel F, Targan S, Gunvar T. Ozkan H, et al. Among authors: genel f. J Investig Allergol Clin Immunol. 2005;15(1):69-74. J Investig Allergol Clin Immunol. 2005. PMID: 15864886

10

Fulminant amoebiasis in a child with recurrent multiple amoebic liver abscesses and pleuropulmonary complications.

Genel F, Atlihan F, Targan S, Gulez N, Hacikara S, Karaca I. Genel F, et al. Ann Trop Paediatr. 2004 Sep;24(3):267-9. doi: 10.1179/027249304225019019. Ann Trop Paediatr. 2004. PMID: 15479578

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