Beck 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: beck 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

Urinary NAG in children with urolithiasis, nephrocalcinosis, or risk of urolithiasis.

Sikora P, Glatz S, Beck BB, Stapenhorst L, Zajaczkowska M, Hesse A, Hoppe B. Sikora P, et al. Among authors: beck bb. Pediatr Nephrol. 2003 Oct;18(10):996-9. doi: 10.1007/s00467-003-1229-7. Epub 2003 Aug 13. Pediatr Nephrol. 2003. PMID: 12920632

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: beck 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

4

Hypocitraturia as a risk factor for nephrocalcinosis after kidney transplantation.

Stapenhorst L, Sassen R, Beck B, Laube N, Hesse A, Hoppe B. Stapenhorst L, et al. Among authors: beck b. Pediatr Nephrol. 2005 May;20(5):652-6. doi: 10.1007/s00467-005-1831-y. Epub 2005 Mar 22. Pediatr Nephrol. 2005. PMID: 15782300

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: beck 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

Oxalobacter formigenes: a potential tool for the treatment of primary hyperoxaluria type 1.

Hoppe B, Beck B, Gatter N, von Unruh G, Tischer A, Hesse A, Laube N, Kaul P, Sidhu H. Hoppe B, et al. Among authors: beck b. Kidney Int. 2006 Oct;70(7):1305-11. doi: 10.1038/sj.ki.5001707. Epub 2006 Jul 19. Kidney Int. 2006. PMID: 16850020 Free article. Clinical Trial.

7

Is there a genotype-phenotype correlation in primary hyperoxaluria type 1?

Beck BB, Hoppe B. Beck BB, et al. Kidney Int. 2006 Sep;70(6):984-6. doi: 10.1038/sj.ki.5001797. Kidney Int. 2006. PMID: 16957746 Free article.

8

The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect.

Wolf MT, Beck BB, Zaucke F, Kunze A, Misselwitz J, Ruley J, Ronda T, Fischer A, Eifinger F, Licht C, Otto E, Hoppe B, Hildebrandt F. Wolf MT, et al. Among authors: beck bb. Kidney Int. 2007 Mar;71(6):574-81. doi: 10.1038/sj.ki.5002089. Epub 2007 Jan 24. Kidney Int. 2007. PMID: 17245395 Free article.

9

[13C2]oxalate absorption in children with idiopathic calcium oxalate urolithiasis or primary hyperoxaluria.

Sikora P, von Unruh GE, Beck B, Feldkötter M, Zajaczkowska M, Hesse A, Hoppe B. Sikora P, et al. Among authors: beck b. Kidney Int. 2008 May;73(10):1181-6. doi: 10.1038/ki.2008.63. Epub 2008 Mar 12. Kidney Int. 2008. PMID: 18337715 Free article.

10

The case: A boy with recurrent stones.

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

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