Study programme
Classes
Publications
- Congenital myopathies +12012 | Second Faculty of Medicine
- Corneal Ulceration Complicating Surgical Correction of Ptosis in Patient with Kearns-Sayre Syndrome - a Case Report2011 | Second Faculty of Medicine
- Myoclonic Epilepsy and Deafness in Siblings with the 7512T>C Mutation in the Mitochondrial Encoded tRNA(Ser(UCN)) Gene - Case Reports2010 | Faculty of Science, Faculty of Physical Education and Sport, First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Myoclonic Epilepsy and Deafness in Siblings with the 7512T > C Mutation in the Mitochondrial Encoded tRNA(Ser(UCN)) Gene - Case Reports2010 | Second Faculty of Medicine
- Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients2006 | Second Faculty of Medicine
- Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)2006 | Second Faculty of Medicine
- Molecular-pathologic and genetic diagnostics of limb girdle muscular dystrophy LGMD2A: presentation of first cases diagnosed in the Czech Republic2004 | Second Faculty of Medicine
- Longitudinal and multidisciplinar care about the patients and families suffering from proximal muscular dystrophyPublication without faculty affiliation
- 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
Loading network view...