Publikace
- Cardiac profile of the Czech population of Duchenne muscular dystrophy patients: a cardiovascular magnetic resonance study with T1 mapping2019 | 2. lékařská fakulta
- Six New Gap Junction Beta 1 Gene Mutations and Their Phenotypic Expression in Czech Patients with Charcot-Marie-Tooth Disease2010 | 2. lékařská fakulta
- Mutations in the LMNA gene do not cause axonal CMT in Czech patients2009 | 2. lékařská fakulta
- Point mutations in Czech DMD/BMD patients and their phenotypic outcome2009 | 2. lékařská fakulta
- Hereditary spastic paraplegia 3A associated with axonal neuropathy2007 | 2. lékařská fakulta
- SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve2004 | 2. lékařská fakulta
- Efficacy and Safety of Vamorolone Over 48 Weeks in Boys With Duchenne Muscular Dystrophy: A Randomized Controlled Trial2024 | 2. lékařská fakulta
- Dětská pneumologie2023 | 1. lékařská fakulta, 2. lékařská fakulta, Fakulta tělesné výchovy a sportu, 3. lékařská fakulta
- A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype-phenotype correlation2023 | 1. lékařská fakulta, 2. lékařská fakulta
- Genetic findings in Czech patients with limb girdle muscular dystrophy2023 | 1. lékařská fakulta, 2. lékařská fakulta
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