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autosomal
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Tolvaptan in patients with autosomal dominant polycystic kidney disease. Commentary on: NEJM 2012,Torres:Tolvaptan in patients with autosomal dominant polycystic kidney disease
2012 |
First Faculty of Medicine
publication
Autosomal dominant spinocerebellar ataxias
2005 |
Second Faculty of Medicine
publication
Autosomal dominant spinocerebellar ataxias: Review
2018 |
Faculty of Medicine in Pilsen
publication
Autosomal Dominant Tubulointerstitial Kidney Disease
2017 |
First Faculty of Medicine
publication
Autosomal recessive and X-linked ataxia
2007 |
Second Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease: A review
2022 |
First Faculty of Medicine
publication
Spinocerebellar ataxias. Part II. Problematics of autosomal dominant spinocerebellar ataxias
2001 |
Second Faculty of Medicine
publication
The Pendred syndrome - the remarks to autosomal reesive hearing loss associated with goitr
2004 |
Faculty of Physical Education and Sport
publication
Autosomal Recessive and Dominant Polycystic Kidney Disease
1999 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Hypomagnesaemia is absent in children with autosomal dominant polycystic kidney disease
2019 |
Second Faculty of Medicine
publication
The Correlation of Genotype and Phenotype in Children with Autosomal Dominant Polycystic Kidney Disease
Publication without faculty affiliation
publication
Autosomal dominant tubulointerstitial kidney disease: more than just HNF1 beta
2022 |
First Faculty of Medicine
publication
Molecular Genetic Background of an Autosomal Dominant Hypercholesterolemia in the Czech Republic
2017 |
First Faculty of Medicine
publication
Autosomal dominant polycystic kidney disease from urological point of view
2023 |
Faculty of Medicine in Hradec Králové
publication
Proteinuria in children with autosomal dominant polycystic kidney disease
2018 |
Second Faculty of Medicine
publication
Autosomal Dominant Polycystic Kidney Disease: From Pathophysiology of Cystogenesis to Advances in the Treatment
2022 |
First Faculty of Medicine
publication
New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease
2009 |
First Faculty of Medicine
publication
Spanish guidelines for the management of autosomal dominant polycystic kidney disease
2015 |
First Faculty of Medicine
publication
New European recommendations for the treatment with tolvaptan in patients with autosomal dominant polycystic kidneys
2021 |
First Faculty of Medicine
publication
DNA analysis of autosomal polycystic kidney disease in Czech Republic
2001 |
Faculty of Physical Education and Sport
publication
Genotype phenotype spectrum of PYCR1-related autosomal recessive cutis laxa
2013 |
Second Faculty of Medicine
publication
M TOR inhibitor everolimus in patients in with autosomal dominant polycystic kidney disease.Commentary on:NEJM 363,2010
2010 |
First Faculty of Medicine
publication
Quality of life in patients with autosomal dominant tubulointerstitial kidney disease
2019 |
First Faculty of Medicine
publication
Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease
2023 |
First Faculty of Medicine
publication
Genotype–phenotype correlation in children with autosomal dominant polycystic kidney disease
2009 |
First Faculty of Medicine
publication
Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)
2020 |
Second 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
Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele
2013 |
First Faculty of Medicine
publication
Influence of endothelin-1 gene polymorphisms on the progression of autosomal dominant polycystic kidney disease
2006 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
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