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Leigh syndrome
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RNDr. Robert Ivánek Ph.D.
External person at First Faculty of Medicine
22 publications
Publications
publication
Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis
2011 |
First Faculty of Medicine
publication
Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure
2009 |
First Faculty of Medicine
publication
HIF and reactive oxygen species regulate oxidative phosphorylation in cancer
2008 |
First Faculty of Medicine
publication
Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated FIFo ATP synthase deficiency
2008 |
First Faculty of Medicine
publication
TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy
2008 |
First Faculty of Medicine
publication
Rotor-type hyperbilirubinaemia has no defect in the canalicular bilirubin export pump
2007 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Rotor-type hyperbilirubinaemia has no defect in the canalicular bilirubin export pump
2007 |
Faculty of Physical Education and Sport
publication
Mutation in TMEM76 cause mucopolysacharidosis III C syndrome
2006 |
First Faculty of Medicine
publication
Mutation in TMEM76 cause mucopolysacharidosis III C syndrome
2006 |
Faculty of Physical Education and Sport
publication
The use of Comparative Duplex PCR in Monitoring of Patients with Non-Hodgkin´s Lymphoma and Chronic Lymphocytic Leukaemia
2005 |
First Faculty of Medicine
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