Publications by authors named "Petr Vylet'al"

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Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational study.
Kendrah O Kidd, Adrienne H Williams, Abbigail Taylor, Lauren Martin, Victoria Robins, Petr Vylet'al

BMC Nephrol· December 2024

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Eight-Fold Increased COVID-19 Mortality in Autosomal Dominant Tubulointerstitial Kidney Disease due to Mutations: An Observational Study.
Kendrah O Kidd, Adrienne H Williams, Abbigail Taylor, Lauren Martin, Victoria Robins, Petr Vylet'al

medRxiv· July 2024

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Bi-allelic Mutations and Undetectable Plasma Renin Activity in a Patient With Progressive CKD.
Sofia Jorge, Kendrah Kidd, Petr Vylet'al, Estela Nogueira, Lauren Martin

Kidney Int Rep· May 2023

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Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations.
Petr Vylet'al, Kendrah Kidd, Hannah C Ainsworth, Drahomíra Springer, Alena Vrbacká

Am J Nephrol· January 2022

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Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to Mutations.
Kendrah Kidd, Petr Vylet'al, Céline Schaeffer, Eric Olinger, Martina Živná

Kidney Int Rep· September 2020

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Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1.
Anthony J Bleyer, Stanislav Kmoch, Corinne Antignac, Vicki Robins, Kendrah Kidd, Petr Vylet'al

Clin J Am Soc Nephrol· March 2014

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Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Andrew Kirby, Andreas Gnirke, David B Jaffe, Veronika Barešová, Nathalie Pochet, Petr Vylet'al

Nat Genet· March 2013

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Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure.
Martina Zivná, Helena Hůlková, Marie Matignon, Katerina Hodanová, Petr Vylet'al

Am J Hum Genet· August 2009

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Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes.
Blanka Stibůrková, Jacek Majewski, Katerina Hodanová, Lenka Ondrová, Markéta Jerábková, Petr Vylet'al

Eur J Hum Genet· February 2003

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