Total number of publications: 57
2023
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Myocardial native T1 mapping and extracellular volume quantification in asymptomatic female carriers of Duchenne muscular dystrophy gene mutations
Orphanet Journal of Rare Diseases, year: 2023, volume: 18, edition: 1, DOI
2022
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Kongenitální svalové dystrofie
Neurol. praxi, year: 2022, edition: 23
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Možnosti časné diagnostiky Duchennovy svalové dystrofie- doporučení pro pediatry.
Neurol. praxi, year: 2022, volume: 23
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Neuropsychiatrické komorbidity u pacientů s Duchennovou svalovou dystrofií.
Neurol. praxi, year: 2022, volume: 23
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Prognostic factors and seizure outcome in posterior reversible encephalopathy syndrome (PRES) in children with malignancies.
Year: 2022, type: Conference abstract
2021
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Decreased Global Strains of LV in Asymptomatic Female Duchenne Muscular Dystrophy Gene Carriers Using CMR-FT
JACC: Cardiovascular Imaging, year: 2021, volume: 14, edition: 5, DOI
2020
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Anti-Mullerian hormone as an ovarian reserve marker in women with the most frequent muscular dystrophies
Medicine, year: 2020, volume: 99, edition: 23, DOI
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Echocardiographic signs of subclinical cardiac function impairment in Duchenne dystrophy gene carriers
Scientific Reports, year: 2020, volume: 10, edition: 1, DOI
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Léčba Duchennovy svalové dystrofie
Neurologia, year: 2020, volume: 15, edition: 1
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Role neurologa v multidisciplinární péči o pacienty se spinální muskulární atrofií
Ceska a slovenska neurologie a neurochirurgie, year: 2020, volume: 83, edition: Supplementum 2, DOI