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List of works by Petr Vyletal

Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversion

scientific article published on March 2007

Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure

scientific article

Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia

scientific journal article

Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41

scientific article published on 01 October 2005

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

scientific article

Noninvasive Immunohistochemical Diagnosis and Novel Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease

scientific article published on 02 July 2018

Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type I.

scientific article published on 22 September 2011

Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases

scientific article published on 24 July 2019

Quality of life in patients with autosomal dominant tubulointerstitial kidney disease

Uromodulin Biology and Pathophysiology – An Update ⬇️

scientific article published on November 25, 2010

Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1

scientific article published on 07 February 2014

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