Lindner TH - Search Results

1

Secreted frizzled-related protein 4 predicts progression of autosomal dominant polycystic kidney disease.

Zschiedrich S, Budde K, Nürnberger J, Wanner C, Sommerer C, Kunzendorf U, Banas B, Hoerl WH, Obermüller N, Arns W, Pavenstädt H, Gaedeke J, Lindner TH, Faerber L, Wimmer P, Stork R, Eckardt KU, Walz G. Zschiedrich S, et al. Among authors: lindner th. Nephrol Dial Transplant. 2016 Feb;31(2):284-9. doi: 10.1093/ndt/gfv077. Epub 2015 Apr 1. Nephrol Dial Transplant. 2016. PMID: 25832108

2

Diabetic nephropathy: an inherited disease or just a diabetic complication?

Berger M, Mönks D, Wanner C, Lindner TH. Berger M, et al. Among authors: lindner th. Kidney Blood Press Res. 2003;26(3):143-54. doi: 10.1159/000071880. Kidney Blood Press Res. 2003. PMID: 12886042 Review.

3

Genetic aspects of diabetic nephropathy.

Lindner TH, Mönks D, Wanner C, Berger M. Lindner TH, et al. Kidney Int Suppl. 2003 May;(84):S186-91. doi: 10.1046/j.1523-1755.63.s84.24.x. Kidney Int Suppl. 2003. PMID: 12694341 Free article. Review.

4

Hidden population substructures in an apparently homogeneous population bias association studies.

Berger M, Stassen HH, Köhler K, Krane V, Mönks D, Wanner C, Hoffmann K, Hoffmann MM, Zimmer M, Bickeböller H, Lindner TH. Berger M, et al. Among authors: lindner th. Eur J Hum Genet. 2006 Feb;14(2):236-44. doi: 10.1038/sj.ejhg.5201546. Eur J Hum Genet. 2006. PMID: 16333311

5

Alternative approach for rapid and reliable single-nucleotide polymorphism typing with double restriction mutagenesis primer PCR.

Berger M, Zschemisch S, Hocher B, Mönks D, Slowinski T, Halle H, Wanner C, Walter U, Lindner TH. Berger M, et al. Among authors: lindner th. Clin Chem. 2004 Dec;50(12):2376-8. doi: 10.1373/clinchem.2004.036137. Clin Chem. 2004. PMID: 15563486 No abstract available.

6

Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease.

Ottlewski I, Münch J, Wagner T, Schönauer R, Bachmann A, Weimann A, Hentschel J, Lindner TH, Seehofer D, Bergmann C, Jamra RA, Halbritter J. Ottlewski I, et al. Among authors: lindner th. Kidney Int. 2019 Jul;96(1):222-230. doi: 10.1016/j.kint.2019.01.038. Epub 2019 Mar 15. Kidney Int. 2019. PMID: 31027891 Free article.

7

HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing.

Seifert W, Beninde J, Hoffmann K, Lindner TH, Bassir C, Aksu F, Hübner C, Verbeek NE, Mundlos S, Horn D. Seifert W, et al. Among authors: lindner th. Eur J Hum Genet. 2009 Dec;17(12):1570-6. doi: 10.1038/ejhg.2009.104. Epub 2009 Jul 1. Eur J Hum Genet. 2009. PMID: 19568269 Free PMC article.

8

Are glucokinase mutations associated with low triglycerides?

Berger M, Mönks D, Schmidt H, Krane V, Wanner C, Walter U, Lindner TH. Berger M, et al. Among authors: lindner th. Clin Chem. 2005 Apr;51(4):791-3. doi: 10.1373/clinchem.2004.045963. Clin Chem. 2005. PMID: 15788789 No abstract available.

9

The diagnostic value of native kidney biopsy in low grade, subnephrotic, and nephrotic range proteinuria: A retrospective cohort study.

de Fallois J, Schenk S, Kowald J, Lindner TH, Engesser M, Münch J, Meigen C, Halbritter J. de Fallois J, et al. Among authors: lindner th. PLoS One. 2022 Sep 2;17(9):e0273671. doi: 10.1371/journal.pone.0273671. eCollection 2022. PLoS One. 2022. PMID: 36054109 Free PMC article.

10

A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1.

Schönberger J, Kühler L, Martins E, Lindner TH, Silva-Cardoso J, Zimmer M. Schönberger J, et al. Among authors: lindner th. Hum Genet. 2005 Dec;118(3-4):451-7. doi: 10.1007/s00439-005-0064-2. Epub 2005 Oct 14. Hum Genet. 2005. PMID: 16228230

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