Publications by authors named "J Indrakova"

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NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis.
Michaela Sibikova, Filip Fencl, Jan David, Karel Vondrak, Nadezda Simankova, Jana Indrakova

Klin Padiatr· July 2024

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The First Pediatric Case of an IFT140 Heterozygous Deletion Causing Autosomal Dominant Polycystic Kidney Disease: Case Report.
Tomáš Seeman, Terezie Šuláková, Alice Bosáková, Jana Indráková, Dagmar Grečmalová

Case Rep Nephrol Dial· July 2024

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Persistent Flaccid Paralysis in a Patient with Bartter Syndrome.
Vlasta Krejcova, Jan David, Adam Svepes, Irena Buksakowska, Eva Kantorova, Jana Indrakova

Klin Padiatr· September 2023

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A founder pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people.
Pavlina Plevova, Jana Indrakova, Judy Savige, Petra Kuhnova, Petra Tvrda

Front Med (Lausanne)· February 2023

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Multigene Panel Germline Testing of 1333 Czech Patients with Ovarian Cancer.
Klara Lhotova, Lenka Stolarova, Petra Zemankova, Michal Vocka, Marketa Janatova, Jana Indrakova

Cancers (Basel)· April 2020

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