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HFE gene mutations (C282Y, H63D, S65C)
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Miroslav Votruba
External person at First Faculty of Medicine
6 publications
Publications
publication
AGAL misprocessing-induced ER stress and the unfolded protein response: lysosomal storage-independent mechanism of Fabry disease pathogenesis?
2022 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases
2020 |
First Faculty of Medicine
publication
Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations
2020 |
First Faculty of Medicine
publication
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes
2020 |
First Faculty of Medicine
publication
Quality of life in patients with autosomal dominant tubulointerstitial kidney disease
2019 |
First Faculty of Medicine
publication
Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease
2018 |
First Faculty of Medicine, Second Faculty of Medicine
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