Study programme
Classes
Publications
- Different laboratory and muscle biopsy findings in a family with an m.8851T > C mutation in the mitochondrial MTATP6 gene2013 | First Faculty of Medicine, Second Faculty of Medicine
- Immunoexpression of type-1 adiponectin receptor in the human intestine2012 | Second Faculty of Medicine
- Corneal Ulceration Complicating Surgical Correction of Ptosis in Patient with Kearns-Sayre Syndrome - a Case Report2011 | Second Faculty of Medicine
- Dilated cardiomyopathy and mild myopathic syndrome in a 40-year-old man2010 | Second Faculty of Medicine
- Reversible posterior leukoencephalopathy syndrome2008 | Second Faculty of Medicine
- Hereditary spastic paraplegia 3A associated with axonal neuropathy2007 | Second Faculty of Medicine
- Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)2006 | Second Faculty of Medicine
- Unexpected sudden death caused by medullary brain lesions involves all age groups and may include 'sudden infant death syndrome' as a subset2005 | Second Faculty of Medicine, Third Faculty of Medicine
- A 5-year-old boy with super-refractory status epilepticus and RANBP2 variant warranting life-saving hemispherotomy2024 | Second Faculty of Medicine, Central Library of Charles University
- Unusual fusion gene rearrangements in patients with nodular fasciitis: a study of rare and novel USP6 fusion partners with a review of the literature2024 | Second Faculty of Medicine
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