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ADTKD
Publication
Class
Person
Publication
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publication
Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland
2019 |
First Faculty of Medicine
publication
Finding the genetic causes of chronic kidney disease
2021 |
First Faculty of Medicine
publication
Renal transplant outcomes in patients with autosomal dominant tubulointerstitial kidney disease
2020 |
First Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease: A review
2022 |
First Faculty of Medicine
publication
Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease
2023 |
First Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease
2018 |
First Faculty of Medicine
publication
Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1
2020 |
First Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease: more than just HNF1 beta
2022 |
First Faculty of Medicine
publication
Ultrabright plasmonic fluor nanolabel-enabled detection of a urinary ER stress biomarker in autosomal dominant tubulointerstitial kidney disease
2021 |
First Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease
2019 |
First Faculty of Medicine
publication
Identification of a novel UMOD mutation (c. 163G > A) in a Brazilian family with autosomal dominant tubulointerstitial kidney disease
2018 |
First Faculty of Medicine
publication
Quality of life in patients with autosomal dominant tubulointerstitial kidney disease
2019 |
First Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease: of names and genes
2014 |
First Faculty of Medicine
publication
MANF stimulates autophagy and restores mitochondrial homeostasis to treat autosomal dominant tubulointerstitial kidney disease in mice
2023 |
First Faculty of Medicine
publication
Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia
2016 |
First Faculty of Medicine
publication
An intermediate-effect size variant in UMOD confers risk for chronic kidney disease
2022 |
First Faculty of Medicine
publication
Autosomal Dominant Tubulointerstitial Kidney Disease
2017 |
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
Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease
2018 |
First Faculty of Medicine, Second 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
Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases
2020 |
First Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management-A KDIGO consensus report
2015 |
First Faculty of Medicine
publication
Phenylbutyrate rescues the transport defect of the Sec61α mutations V67G and T185A for renin
2022 |
First Faculty of Medicine
publication
Influence of glycoprotein MUC1 on trafficking of the Ca2+-selective ion channels, TRPV5 and TRPV6, and on in vivo calcium homeostasis
2023 |
First Faculty of Medicine
publication
Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations
2021 |
First Faculty of Medicine, Faculty of Medicine in Pilsen