Hoppe B - Search Results

1

A classic twin study of lower urinary tract obstruction: Report of 3 cases and literature review.

Frese S, Weigert A, Hoppe B, Feldkötter M, Ludwig M, Weber S, Kiliś-Pstrusińska K, Zaniew M, Reutter H, Hilger AC. Frese S, et al. Among authors: hoppe b. Low Urin Tract Symptoms. 2019 Apr;11(2):O85-O88. doi: 10.1111/luts.12222. Epub 2018 Apr 17. Low Urin Tract Symptoms. 2019. PMID: 29664229 Review.

2

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.

3

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

4

Liver fibrosis in recessive multicystic kidney diseases: transient elastography for early detection.

Kummer S, Sagir A, Pandey S, Feldkötter M, Habbig S, Körber F, Ney D, Hoppe B, Häussinger D, Mayatepek E, Oh J. Kummer S, et al. Among authors: hoppe b. Pediatr Nephrol. 2011 May;26(5):725-31. doi: 10.1007/s00467-011-1771-7. Epub 2011 Feb 1. Pediatr Nephrol. 2011. PMID: 21279811

5

Cardiorespiratory capacity in children and adolescents on maintenance haemodialysis.

Schaar B, Feldkötter M, Nonn JM, Hoppe B. Schaar B, et al. Among authors: hoppe b. Nephrol Dial Transplant. 2011 Nov;26(11):3701-8. doi: 10.1093/ndt/gfr014. Epub 2011 Mar 4. Nephrol Dial Transplant. 2011. PMID: 21378148

6

Liquid chromatography-tandem mass spectrometry method for the quantification of mycophenolic acid and its phenolic glucuronide in saliva and plasma using a standardized saliva collection device.

Wiesen MH, Farowski F, Feldkötter M, Hoppe B, Müller C. Wiesen MH, et al. Among authors: hoppe b. J Chromatogr A. 2012 Jun 8;1241:52-9. doi: 10.1016/j.chroma.2012.04.008. Epub 2012 Apr 11. J Chromatogr A. 2012. PMID: 22552204

7

Prospective study on the potential of RAAS blockade to halt renal disease in Alport syndrome patients with heterozygous mutations.

Stock J, Kuenanz J, Glonke N, Sonntag J, Frese J, Tönshoff B, Höcker B, Hoppe B, Feldkötter M, Pape L, Lerch C, Wygoda S, Weber M, Müller GA, Gross O. Stock J, et al. Among authors: hoppe b. Pediatr Nephrol. 2017 Jan;32(1):131-137. doi: 10.1007/s00467-016-3452-z. Epub 2016 Jul 11. Pediatr Nephrol. 2017. PMID: 27402170

8

Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.

Zhang R, Marsch F, Kause F, Degenhardt F, Schmiedeke E, Märzheuser S, Hoppe B, Bachour H, Boemers TM, Schäfer M, Spychalski N, Neser J, Leonhardt J, Kosch F, Ure B, Gómez B, Lacher M, Deffaa OJ, Palta M, Wittekindt B, Kleine K, Schmedding A, Grasshoff-Derr S, Ven AV, Heilmann-Heimbach S, Zwink N, Jenetzky E, Ludwig M, Reutter H. Zhang R, et al. Among authors: hoppe b. Birth Defects Res. 2017 Jul 17;109(13):1063-1069. doi: 10.1002/bdr2.1042. Epub 2017 Jun 12. Birth Defects Res. 2017. PMID: 28605140

9

Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type III.

Ventzke A, Feldkötter M, Wei A, Becker J, Beck BB, Hoppe B. Ventzke A, et al. Among authors: hoppe b. Pediatr Nephrol. 2017 Dec;32(12):2263-2271. doi: 10.1007/s00467-017-3731-3. Epub 2017 Jul 15. Pediatr Nephrol. 2017. PMID: 28711958

10

Correction to: Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow up of primary hyperoxaluria type III.

Ventzke A, Feldkötter M, Wei A, Becker J, Beck BB, Hoppe B. Ventzke A, et al. Among authors: hoppe b. Pediatr Nephrol. 2018 Jul;33(7):1275-1276. doi: 10.1007/s00467-018-3944-0. Pediatr Nephrol. 2018. PMID: 29637271

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