Licht C - Search Results

1

Von Willebrand factor regulates complement on endothelial cells.

Noone DG, Riedl M, Pluthero FG, Bowman ML, Liszewski MK, Lu L, Quan Y, Balgobin S, Schneppenheim R, Schneppenheim S, Budde U, James P, Atkinson JP, Palaniyar N, Kahr WH, Licht C. Noone DG, et al. Among authors: licht c. Kidney Int. 2016 Jul;90(1):123-34. doi: 10.1016/j.kint.2016.03.023. Epub 2016 May 25. Kidney Int. 2016. PMID: 27236750 Free PMC article.

2

Two novel ADAMTS13 gene mutations in thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome (TTP/HUS).

Licht C, Stapenhorst L, Simon T, Budde U, Schneppenheim R, Hoppe B. Licht C, et al. Kidney Int. 2004 Sep;66(3):955-8. doi: 10.1111/j.1523-1755.2004.00841.x. Kidney Int. 2004. PMID: 15327386 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. 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

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. 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.

5

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: licht c. 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.

6

Platelet-associated complement factor H in healthy persons and patients with atypical HUS.

Licht C, Pluthero FG, Li L, Christensen H, Habbig S, Hoppe B, Geary DF, Zipfel PF, Kahr WH. Licht C, et al. Blood. 2009 Nov 12;114(20):4538-45. doi: 10.1182/blood-2009-03-205096. Epub 2009 Aug 24. Blood. 2009. PMID: 19704120 Free article.

7

Antibody mediated rejection associated with complement factor h-related protein 3/1 deficiency successfully treated with eculizumab.

Noone D, Al-Matrafi J, Tinckam K, Zipfel PF, Herzenberg AM, Thorner PS, Pluthero FG, Kahr WH, Filler G, Hebert D, Harvey E, Licht C. Noone D, et al. Among authors: licht c. Am J Transplant. 2012 Sep;12(9):2546-53. doi: 10.1111/j.1600-6143.2012.04124.x. Epub 2012 Jun 8. Am J Transplant. 2012. PMID: 22681773 Free article.

8

An update on the pathomechanisms and future therapies of Alport syndrome.

Noone D, Licht C. Noone D, et al. Among authors: licht c. Pediatr Nephrol. 2013 Jul;28(7):1025-36. doi: 10.1007/s00467-012-2272-z. Epub 2012 Aug 18. Pediatr Nephrol. 2013. PMID: 22903660 Review.

9

Monitoring and modeling treatment of atypical hemolytic uremic syndrome.

Heinen S, Pluthero FG, van Eimeren VF, Quaggin SE, Licht C. Heinen S, et al. Among authors: licht c. Mol Immunol. 2013 May;54(1):84-8. doi: 10.1016/j.molimm.2012.10.044. Epub 2012 Dec 3. Mol Immunol. 2013. PMID: 23220071

10

Chronic kidney disease: a new look at pathogenetic mechanisms and treatment options.

Noone D, Licht C. Noone D, et al. Among authors: licht c. Pediatr Nephrol. 2014 May;29(5):779-92. doi: 10.1007/s00467-013-2436-5. Epub 2013 Mar 8. Pediatr Nephrol. 2014. PMID: 23471475 Review.

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