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Mechanisms of pathogenicity and the quest for genetic modifiers of kidney disease in branchiootorenal syndrome.
Clin Kidney J. 2023 Oct 13;17(1):sfad260. doi: 10.1093/ckj/sfad260. eCollection 2024 Jan.
Clin Kidney J. 2023.
PMID: 38213489
Free PMC article.
Novel somatic PBX1 mosaicism likely masking syndromic CAKUT in an adult with bilateral kidney hypoplasia.
Petzold F, Jin W, Hantmann E, Korbach K, Schönauer R, Halbritter J.
Petzold F, et al.
Clin Kidney J. 2022 Apr 6;15(7):1333-1339. doi: 10.1093/ckj/sfac092. eCollection 2022 Jul.
Clin Kidney J. 2022.
PMID: 35756743
Free PMC article.
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Clinical and Functional Assessment of Digenicity in Renal Phosphate Wasting.
Petzold F, Schönauer R, Werner A, Halbritter J.
Petzold F, et al.
Nutrients. 2023 Apr 26;15(9):2081. doi: 10.3390/nu15092081.
Nutrients. 2023.
PMID: 37432176
Free PMC article.
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Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes.
Schönauer R, Baatz S, Nemitz-Kliemchen M, Frank V, Petzold F, Sewerin S, Popp B, Münch J, Neuber S, Bergmann C, Halbritter J.
Schönauer R, et al. Among authors: petzold f.
Genet Med. 2020 Aug;22(8):1374-1383. doi: 10.1038/s41436-020-0816-3. Epub 2020 May 13.
Genet Med. 2020.
PMID: 32398770
Free PMC article.
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Retrospective genetic analysis illustrates the spectrum of autosomal Alport syndrome in a case of living-related donor kidney transplantation.
Petzold F, Bachmann A, Bergmann C, Helmchen U, Halbritter J.
Petzold F, et al.
BMC Nephrol. 2019 Sep 2;20(1):340. doi: 10.1186/s12882-019-1523-7.
BMC Nephrol. 2019.
PMID: 31477057
Free PMC article.
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Delta weight loss unlike genetic variation associates with hyperoxaluria after malabsorptive bariatric surgery.
Scherer L, Schönauer R, Nemitz-Kliemchen M, Hagemann T, Hantmann E, de Fallois J, Petzold F, Blüher M, Halbritter J.
Scherer L, et al. Among authors: petzold f.
Sci Rep. 2023 Jun 3;13(1):9029. doi: 10.1038/s41598-023-35941-8.
Sci Rep. 2023.
PMID: 37270618
Free PMC article.
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Evaluating pathogenicity of SLC34A3-Ser192Leu, a frequent European missense variant in disorders of renal phosphate wasting.
Schönauer R, Petzold F, Lucinescu W, Seidel A, Müller L, Neuber S, Bergmann C, Sayer JA, Werner A, Halbritter J.
Schönauer R, et al. Among authors: petzold f.
Urolithiasis. 2019 Dec;47(6):511-519. doi: 10.1007/s00240-019-01116-2. Epub 2019 Feb 23.
Urolithiasis. 2019.
PMID: 30798342
Free PMC article.
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Extended genomic HLA typing identifies previously unrecognized mismatches in living kidney transplantation.
Lehmann C, Pehnke S, Weimann A, Bachmann A, Dittrich K, Petzold F, Fürst D, de Fallois J, Landgraf R, Henschler R, Lindner TH, Halbritter J, Doxiadis I, Popp B, Münch J.
Lehmann C, et al. Among authors: petzold f.
Front Immunol. 2023 Jan 27;14:1094862. doi: 10.3389/fimmu.2023.1094862. eCollection 2023.
Front Immunol. 2023.
PMID: 36776892
Free PMC article.
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