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doc. MUDr. Dana Šafka Brožková Ph.D.
Academic staff at Second Faculty of Medicine
37 publications
Publications
publication
Demyelinating Charcot Marie Tooth neuropathy associated with FBLN5 mutations
2020 |
Second Faculty of Medicine
publication
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene
2019 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population
2018 |
Second Faculty of Medicine
publication
Improving diagnosis of inherited peripheral neuropathies through gene panel analysis
2016 |
Second Faculty of Medicine
publication
MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin
2015 |
Second Faculty of Medicine
publication
Hereditary neuropathy
+1
2015 |
Second Faculty of Medicine
publication
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay
2014 |
Second Faculty of Medicine
publication
Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous woman
2013 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Science
publication
A progressive KY myopathy could be caused by a missense pathogenic variant
2023 |
Second Faculty of Medicine
publication
The cause of hereditary hearing loss in GJB2 heterozygotes-a comprehensive study of the GJB2/DFNB1 region
2021 |
Second Faculty of Medicine
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