Beck BB - Search Results

1

Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation type.

Mandrile G, van Woerden CS, Berchialla P, Beck BB, Acquaviva Bourdain C, Hulton SA, Rumsby G; OxalEurope Consortium. Mandrile G, et al. Among authors: beck bb. Kidney Int. 2014 Dec;86(6):1197-204. doi: 10.1038/ki.2014.222. Epub 2014 Jul 2. Kidney Int. 2014. PMID: 24988064 Free article.

2

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. 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.

3

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.

4

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.

5

[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. 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.

6

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.

7

The primary hyperoxalurias.

Hoppe B, Beck BB, Milliner DS. Hoppe B, et al. Among authors: beck bb. 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.

8

Novel human pathological mutations. Gene symbol: AGXT. Disease: hyperoxaluria.

Robbiano A, Mandrile G, De Marchi M, Beck B, Baasner A, Murer L, Benetti E, Giachino D. Robbiano A, et al. Hum Genet. 2010 Apr;127(4):468. Hum Genet. 2010. PMID: 21488232 No abstract available.

9

Reduction of plasma oxalate levels by oral application of Oxalobacter formigenes in 2 patients with infantile oxalosis.

Hoppe B, Dittlich K, Fehrenbach H, Plum G, Beck BB. Hoppe B, et al. Among authors: beck bb. Am J Kidney Dis. 2011 Sep;58(3):453-5. doi: 10.1053/j.ajkd.2011.05.012. Epub 2011 Jun 25. Am J Kidney Dis. 2011. PMID: 21705122

10

Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD.

Beck BB, Trachtman H, Gitman M, Miller I, Sayer JA, Pannes A, Baasner A, Hildebrandt F, Wolf MT. Beck BB, et al. Am J Kidney Dis. 2011 Nov;58(5):821-5. doi: 10.1053/j.ajkd.2011.06.029. Epub 2011 Sep 8. Am J Kidney Dis. 2011. PMID: 21903317 Free PMC article.

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