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Meszarosova, Anna Uhrova
25
results:
Search for persons
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Format
Online (25)
Mediatypes
Articles (Online) (17)
OpenAccess-fulltext (8)
Languages
english (21)
Sorted by: Year
Sorted by: Relevance
?
1
Genetic testing in children enrolled in epilepsy surgery pr..:
Straka, Barbora
;
Splitkova, Barbora
;
Vlckova, Marketa
...
European Journal of Paediatric Neurology. 47 (2023) - p. 80-87 , 2023
Link:
https://doi.org/10.1016/..
?
2
Anterior pallidal hyperintensity mimicking the eye of the t..:
Somaya, Vinisha
;
Meszarosova, Anna Uhrova
;
Dusek, Petr
Neurological Sciences. 45 (2023) 2 - p. 799-801 , 2023
Link:
https://doi.org/10.1007/..
?
3
The Instrumental Activities of Daily Living in Parkinson's ..:
Bezdicek, Ondrej
;
Mana, Josef
;
Růžička, Filip
...
Frontiers in Aging Neuroscience. 14 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
4
Biallelic variants in HPDL cause pure and complicated hered..:
Wiessner, Manuela
;
Maroofian, Reza
;
Ni, Meng-Yuan
...
Brain. 144 (2021) 5 - p. 1422-1434 , 2021
Link:
https://doi.org/10.1093/..
?
5
Dominant KPNA3 Mutations Cause Infantile‐Onset Hereditary S..:
Schob, Claudia
;
Hempel, Maja
;
Safka Brozkova, Dana
...
Annals of Neurology. 90 (2021) 5 - p. 738-750 , 2021
Link:
https://doi.org/10.1002/..
?
6
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:
Safka Brozkova, Dana
;
Uhrova Meszarosova, Anna
;
Lassuthova, Petra
...
Genes. 12 (2021) 5 - p. 684 , 2021
Link:
https://doi.org/10.3390/..
?
7
Erratum to: Biallelic variants in HPDL cause pure and compl..:
Wiessner, Manuela
;
Maroofian, Reza
;
Ni, Meng-Yuan
...
Brain. 144 (2021) 8 - p. e70-e70 , 2021
Link:
https://doi.org/10.1093/..
?
8
GATOR1-related focal cortical dysplasia in epilepsy surgery..:
Benova, Barbora
;
Sanders, Maurits W.C.B.
;
Uhrova-Meszarosova, Anna
...
European Journal of Paediatric Neurology. 30 (2021) - p. 88-96 , 2021
Link:
https://doi.org/10.1016/..
?
9
Biallelic variants in HPDL cause pure and complicated hered..:
Wiessner, Manuela
;
Maroofian, Reza
;
Ni, Meng-Yuan
...
qt3zq3c14v. , 2021
Link:
https://escholarship.org..
?
10
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:
Dana Safka Brozkova
;
Anna Uhrova Meszarosova
;
Petra Lassuthova
...
https://www.mdpi.com/2073-4425/12/5/684. , 2021
Link:
https://doi.org/10.3390/..
?
11
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:
Dana Safka Brozkova
;
Anna Uhrova Meszarosova
;
Petra Lassuthova
...
Human Genomics and Genetic Diseases. , 2021
Link:
https://doi.org/10.3390/..
?
12
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:
Safka Brozkova, Dana
;
Uhrova Meszarosova, Anna
;
Lassuthova, Petra
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147375/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
13
Two types of recessive hereditary spastic paraplegia in Rom..:
Meszarosova, Anna Uhrova
;
Seeman, Pavel
;
Jencik, Jan
...
Neuroscience Letters. 721 (2020) - p. 134800 , 2020
Link:
https://doi.org/10.1016/..
?
14
Expanding the phenotype spectrum associated with pathogenic..:
Čopíková, Jana
;
Paděrová, Jana
;
Románková, Věra
...
Annals of Human Genetics. 84 (2020) 5 - p. 380-392 , 2020
Link:
https://doi.org/10.1111/..
?
15
Clinical and genetic features of five Czech patients with S..:
Doleckova, K.
;
Uhrova, A. Meszarosova
;
Stellmachová, J.
...
Parkinsonism & Related Disorders. 79 (2020) - p. e111 , 2020
Link:
https://doi.org/10.1016/..
1-15