Heinen S - Search Results

1

C3 deposition glomerulopathy due to a functional factor H defect.

Habbig S, Mihatsch MJ, Heinen S, Beck B, Emmel M, Skerka C, Kirschfink M, Hoppe B, Zipfel PF, Licht C. Habbig S, et al. Among authors: heinen s. Kidney Int. 2009 Jun;75(11):1230-1234. doi: 10.1038/ki.2008.354. Epub 2008 Jul 16. Kidney Int. 2009. PMID: 18633337 Free article. No abstract available.

2

Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II).

Licht C, Heinen S, Józsi M, Löschmann I, Saunders RE, Perkins SJ, Waldherr R, Skerka C, Kirschfink M, Hoppe B, Zipfel PF. Licht C, et al. Among authors: heinen s. Kidney Int. 2006 Jul;70(1):42-50. doi: 10.1038/sj.ki.5000269. Epub 2006 Apr 12. Kidney Int. 2006. PMID: 16612335 Free article.

3

Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15.

Licht C, Weyersberg A, Heinen S, Stapenhorst L, Devenge J, Beck B, Waldherr R, Kirschfink M, Zipfel PF, Hoppe B. Licht C, et al. Among authors: heinen s. Am J Kidney Dis. 2005 Feb;45(2):415-21. doi: 10.1053/j.ajkd.2004.10.018. Am J Kidney Dis. 2005. PMID: 15685522

4

Complement and diseases: defective alternative pathway control results in kidney and eye diseases.

Zipfel PF, Heinen S, Józsi M, Skerka C. Zipfel PF, et al. Among authors: heinen s. Mol Immunol. 2006 Jan;43(1-2):97-106. doi: 10.1016/j.molimm.2005.06.015. Mol Immunol. 2006. PMID: 16026839 Review.

5

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency.

Józsi M, Licht C, Strobel S, Zipfel SL, Richter H, Heinen S, Zipfel PF, Skerka C. Józsi M, et al. Among authors: heinen s. Blood. 2008 Feb 1;111(3):1512-4. doi: 10.1182/blood-2007-09-109876. Epub 2007 Nov 15. Blood. 2008. PMID: 18006700 Free article.

6

Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions.

Józsi M, Heinen S, Hartmann A, Ostrowicz CW, Hälbich S, Richter H, Kunert A, Licht C, Saunders RE, Perkins SJ, Zipfel PF, Skerka C. Józsi M, et al. Among authors: heinen s. J Am Soc Nephrol. 2006 Jan;17(1):170-7. doi: 10.1681/ASN.2005080868. Epub 2005 Dec 7. J Am Soc Nephrol. 2006. PMID: 16338962

7

Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells.

Heinen S, Józsi M, Hartmann A, Noris M, Remuzzi G, Skerka C, Zipfel PF. Heinen S, et al. J Am Soc Nephrol. 2007 Feb;18(2):506-14. doi: 10.1681/ASN.2006091069. Epub 2007 Jan 17. J Am Soc Nephrol. 2007. PMID: 17229916

8

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.

Zipfel PF, Edey M, Heinen S, Józsi M, Richter H, Misselwitz J, Hoppe B, Routledge D, Strain L, Hughes AE, Goodship JA, Licht C, Goodship TH, Skerka C. Zipfel PF, et al. Among authors: heinen s. PLoS Genet. 2007 Mar 16;3(3):e41. doi: 10.1371/journal.pgen.0030041. Epub 2007 Feb 1. PLoS Genet. 2007. PMID: 17367211 Free PMC article.

9

Defective complement control of factor H (Y402H) and FHL-1 in age-related macular degeneration.

Skerka C, Lauer N, Weinberger AA, Keilhauer CN, Sühnel J, Smith R, Schlötzer-Schrehardt U, Fritsche L, Heinen S, Hartmann A, Weber BH, Zipfel PF. Skerka C, et al. Among authors: heinen s. Mol Immunol. 2007 Jul;44(13):3398-406. doi: 10.1016/j.molimm.2007.02.012. Epub 2007 Mar 30. Mol Immunol. 2007. PMID: 17399790

10

Thrombotic microangiopathies: new insights and new challenges.

Zipfel PF, Heinen S, Skerka C. Zipfel PF, et al. Among authors: heinen s. Curr Opin Nephrol Hypertens. 2010 Jul;19(4):372-8. doi: 10.1097/MNH.0b013e32833aff4a. Curr Opin Nephrol Hypertens. 2010. PMID: 20539230 Review.

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