Hoppe B - Search Results

1

MPGN II--genetically determined by defective complement regulation?

Licht C, Schlötzer-Schrehardt U, Kirschfink M, Zipfel PF, Hoppe B. Licht C, et al. Among authors: hoppe b. Pediatr Nephrol. 2007 Jan;22(1):2-9. doi: 10.1007/s00467-006-0299-8. Epub 2006 Sep 23. Pediatr Nephrol. 2007. PMID: 17024390

2

Posttransplant lymphoproliferative disease in a child: clinical and molecular characterization.

Licht C, Hell K, Eifinger F, Hoppe B, Querfeld U. Licht C, et al. Among authors: hoppe b. Pediatr Nephrol. 2002 Feb;17(2):79-84. doi: 10.1007/s00467-001-0766-1. Pediatr Nephrol. 2002. PMID: 11875668

3

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. Among authors: hoppe b. Kidney Int. 2004 Sep;66(3):955-8. doi: 10.1111/j.1523-1755.2004.00841.x. Kidney Int. 2004. PMID: 15327386 Free article.

4

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: hoppe b. 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

5

Detection of polyomavirus BK and JC in children with kidney diseases and renal transplant recipients.

Müller A, Beck B, Theilemann K, Stapenhorst L, Licht C, Michalk D, Franzen C, Hoppe B. Müller A, et al. Among authors: hoppe b. Pediatr Infect Dis J. 2005 Sep;24(9):778-81. doi: 10.1097/01.inf.0000178071.05483.1c. Pediatr Infect Dis J. 2005. PMID: 16148843

6

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: hoppe b. 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.

7

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: hoppe b. 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.

8

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. Among authors: hoppe b. 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.

9

DEAP-HUS: deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome.

Zipfel PF, Mache C, Müller D, Licht C, Wigger M, Skerka C; European DEAP-HUS Study Group. Zipfel PF, et al. Pediatr Nephrol. 2010 Oct;25(10):2009-19. doi: 10.1007/s00467-010-1446-9. Epub 2010 Feb 16. Pediatr Nephrol. 2010. PMID: 20157737 Review.

10

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.

Gross O, Licht C, Anders HJ, Hoppe B, Beck B, Tönshoff B, Höcker B, Wygoda S, Ehrich JH, Pape L, Konrad M, Rascher W, Dötsch J, Müller-Wiefel DE, Hoyer P; Study Group Members of the Gesellschaft für Pädiatrische Nephrologie; Knebelmann B, Pirson Y, Grunfeld JP, Niaudet P, Cochat P, Heidet L, Lebbah S, Torra R, Friede T, Lange K, Müller GA, Weber M. Gross O, et al. Among authors: hoppe b. Kidney Int. 2012 Mar;81(5):494-501. doi: 10.1038/ki.2011.407. Epub 2011 Dec 14. Kidney Int. 2012. PMID: 22166847 Free article.

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