Hoppe B - 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: 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.

2

Nephrocalcinosis and urolithiasis in children.

Habbig S, Beck BB, Hoppe B. Habbig S, et al. Among authors: hoppe b. Kidney Int. 2011 Dec;80(12):1278-91. doi: 10.1038/ki.2011.336. Epub 2011 Sep 28. Kidney Int. 2011. PMID: 21956187 Free article.

3

The case: A boy with recurrent stones.

Beck BB, Laube N, Habbig S, Feldkötter M, Fries JW, Hoppe B. Beck BB, et al. Among authors: hoppe b. Kidney Int. 2008 Jul;74(1):133-4. doi: 10.1038/ki.2008.165. Kidney Int. 2008. PMID: 18560364 Free article. No abstract available.

4

The primary hyperoxalurias.

Hoppe B, Beck BB, Milliner DS. Hoppe B, et al. Kidney Int. 2009 Jun;75(12):1264-1271. doi: 10.1038/ki.2009.32. Epub 2009 Feb 18. Kidney Int. 2009. PMID: 19225556 Free PMC article. Review.

5

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.

6

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

7

Renal allograft calcification -- prevalence and etiology in pediatric patients.

Habbig S, Beck BB, Feldkötter M, Körber F, Laffeber C, Verkoelen C, Mihatsch MJ, Hoppe B. Habbig S, et al. Among authors: hoppe b. Am J Nephrol. 2009;30(3):194-200. doi: 10.1159/000217585. Epub 2009 Apr 30. Am J Nephrol. 2009. PMID: 19407442

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

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.

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

629 results

Search Page

Filters