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ADPKD
Publication
Class
Person
Publication
Programmes
publication
Coincidence of ADPKD
Publication without faculty affiliation
publication
Research Report University Hospital clinical trial 156-10-291
Publication without faculty affiliation
publication
Vliv hydrochlorothiazidu a metforminu na diurézu u ADPKD při podávání tolvaptanu
2022 |
First Faculty of Medicine
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DNA analysis of autosomal polycystic kidney disease in Czech Republic
Publication without faculty affiliation
publication
DNA analysis of autosomal polycystic kidney disease in Czech Republic
2001 |
Faculty of Physical Education and Sport
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ADPedKD: A Global Online Platform on the Management of Children With ADPKD
2019 |
Second Faculty of Medicine
publication
Oktreotid LAR u pacientů trpících autozomálně dominantní polycystickou chorobou ledvin (ADPKD) a renální insuficiencí: multicentrická, prospektivní, placebem kontrolovaná, randomizovaná studie ALADIN 2
2019 |
First Faculty of Medicine
publication
Building a network of ADPKD reference centres across Europe: the EuroCYST initiative
2014 |
First Faculty of Medicine
publication
Native nephrectomy in patients with autosomal dominant polycystic kidney disease in the kidney transplant program - single-center retrospective results of 2000-2020
2023 |
Faculty of Medicine in Hradec Králové
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Těžký průběh ADPKD u rodičů asociuje s hypertenzí u dětí
2023 |
First Faculty of Medicine
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Autosomal dominant polycystic kidney disease from urological point of view
2023 |
Faculty of Medicine in Hradec Králové
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Infekce jaterních cyst u pacientů s ADPKD při terapii lanreotidem během multicentrické studie DIPAK-1 : komentář
2017 |
First Faculty of Medicine
publication
Plasma endothelin and urinary levels of some prostanoids in autosomal dominant polycystic kidney disease (ADPKD)
2000 |
First Faculty of Medicine
publication
Three novel mutations of the PKD2 gene in czech families with autosomal dominant polycystic kidney disease (ADPKD) (1)
Publication without faculty affiliation
publication
Prevalence of Hypertension in Children with Early-Stage ADPKD
2018 |
Second Faculty of Medicine
publication
Severity in polycystic liver disease is associated with aetiology and female gender: Results of the International PLD Registry
2019 |
First Faculty of Medicine
publication
Molecular genetic analysis in families with autosomal dominant polycystic kidney disease
Publication without faculty affiliation
publication
Genetic analysis in families with autosomal polycystic kidney disease
Publication without faculty affiliation
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Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report
2018 |
First Faculty of Medicine
publication
Molecular Genetic Analysis in Families with Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Publication without faculty affiliation
publication
Early renal damage in children with autosomal dominant polycystic kidney disease (ADPKD)
1995 |
Central Library of Charles University
publication
The influence of edothellin gene polymorphism on the progrssion of autosomal dominant polycystic kidney disease (ADPKD)
Publication without faculty affiliation
publication
DNA analysis in families with autosomal dominant polycystic kidney disease (ADPKD) in Czech Republic
Publication without faculty affiliation
publication
New European recommendations for the treatment with tolvaptan in patients with autosomal dominant polycystic kidneys
2021 |
First Faculty of Medicine
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Spanish guidelines for the management of autosomal dominant polycystic kidney disease
2015 |
First Faculty of Medicine
publication
Three novel mutations of the PKD2 gene in Czech families with autosomal dominant polycistic kidney disease (ADPKD) (2)
Publication without faculty affiliation
publication
Plasma endothelin and urinary levels of selected prostanoids in autosomal dominant polycistic kidney disease (ADPKD)
Publication without faculty affiliation
publication
Mutations in the non-duplicated region of the PKD1 gene in families with autosomal dominant polycystic kidney disease (ADPKD)
Publication without faculty affiliation
publication
An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International
2022 |
First Faculty of Medicine
publication
Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease
2014 |
First Faculty of Medicine