Weber LT - Search Results

1

Prenatal parental decision-making and postnatal outcome in renal oligohydramnios.

Mehler K, Gottschalk I, Burgmaier K, Volland R, Büscher AK, Feldkötter M, Keller T, Weber LT, Kribs A, Habbig S. Mehler K, et al. Among authors: weber lt. Pediatr Nephrol. 2018 Apr;33(4):651-659. doi: 10.1007/s00467-017-3812-3. Epub 2017 Oct 27. Pediatr Nephrol. 2018. PMID: 29075889

2

Therapeutic drug monitoring in pediatric renal transplantation.

Weber LT. Weber LT. Pediatr Nephrol. 2015 Feb;30(2):253-65. doi: 10.1007/s00467-014-2813-8. Epub 2014 Apr 25. Pediatr Nephrol. 2015. PMID: 24763544 Review.

3

A complicated case of atypical hemolytic uremic syndrome with frequent relapses under eculizumab.

Schalk G, Kirschfink M, Wehling C, Gastoldi S, Bergmann C, Hoppe B, Weber LT. Schalk G, et al. Among authors: weber lt. Pediatr Nephrol. 2015 Jun;30(6):1039-42. doi: 10.1007/s00467-015-3078-6. Epub 2015 Mar 10. Pediatr Nephrol. 2015. PMID: 25752761

4

Mycophenolate Mofetil Therapy in Children With Idiopathic Nephrotic Syndrome: Does Therapeutic Drug Monitoring Make a Difference?

Hackl Á, Cseprekál O, Gessner M, Liebau MC, Habbig S, Ehren R, Müller C, Taylan C, Dötsch J, Weber LT. Hackl Á, et al. Among authors: weber lt. Ther Drug Monit. 2016 Apr;38(2):274-9. doi: 10.1097/FTD.0000000000000258. Ther Drug Monit. 2016. PMID: 26488204

5

Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.

Büscher AK, Beck BB, Melk A, Hoefele J, Kranz B, Bamborschke D, Baig S, Lange-Sperandio B, Jungraithmayr T, Weber LT, Kemper MJ, Tönshoff B, Hoyer PF, Konrad M, Weber S; German Pediatric Nephrology Association (GPN). Büscher AK, et al. Among authors: weber s, weber lt. Clin J Am Soc Nephrol. 2016 Feb 5;11(2):245-53. doi: 10.2215/CJN.07370715. Epub 2015 Dec 14. Clin J Am Soc Nephrol. 2016. PMID: 26668027 Free PMC article.

6

Discontinuation of Eculizumab in a Patient With Atypical Hemolytic Uremic Syndrome Due to a Mutation in CFH.

Habbig S, Bergmann C, Weber LT. Habbig S, et al. Among authors: weber lt. Am J Kidney Dis. 2016 Mar;67(3):532-3. doi: 10.1053/j.ajkd.2015.11.009. Epub 2015 Dec 23. Am J Kidney Dis. 2016. PMID: 26724167 No abstract available.

7

Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGS.

Bartram MP, Habbig S, Pahmeyer C, Höhne M, Weber LT, Thiele H, Altmüller J, Kottoor N, Wenzel A, Krueger M, Schermer B, Benzing T, Rinschen MM, Beck BB. Bartram MP, et al. Among authors: weber lt. Hum Mol Genet. 2016 Mar 15;25(6):1152-64. doi: 10.1093/hmg/ddv638. Epub 2016 Jan 5. Hum Mol Genet. 2016. PMID: 26740551

8

Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy.

Weber S, Strasser K, Rath S, Kittke A, Beicht S, Alberer M, Lange-Sperandio B, Hoyer PF, Benz MR, Ponsel S, Weber LT, Klein HG, Hoefele J. Weber S, et al. Among authors: weber lt. Pediatr Nephrol. 2016 Jun;31(6):941-55. doi: 10.1007/s00467-015-3302-4. Epub 2016 Jan 25. Pediatr Nephrol. 2016. PMID: 26809805

9

Effect of mycophenolic acid in experimental, nontransplant glomerular diseases: new mechanisms beyond immune cells.

Hackl A, Ehren R, Weber LT. Hackl A, et al. Among authors: weber lt. Pediatr Nephrol. 2017 Aug;32(8):1315-1322. doi: 10.1007/s00467-016-3437-y. Epub 2016 Jun 16. Pediatr Nephrol. 2017. PMID: 27312386 Review.

10

Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities.

Hackl A, Mehler K, Gottschalk I, Vierzig A, Eydam M, Hauke J, Beck BB, Liebau MC, Ensenauer R, Weber LT, Habbig S. Hackl A, et al. Among authors: weber lt. Pediatr Nephrol. 2017 May;32(5):791-800. doi: 10.1007/s00467-016-3556-5. Epub 2017 Jan 12. Pediatr Nephrol. 2017. PMID: 28083701

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