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Fajkusova, L.
110
results:
Search for persons
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Format
Online (110)
Mediatypes
Articles (Online) (79)
OpenAccess-fulltext (31)
Languages
english (89)
Sorted by: Relevance
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?
1
Czech national registry of facioscapulohumeral muscular dys..:
Vohanka, S.
;
Parmova, O.
;
Fajkusova, L.
...
Neuromuscular Disorders. 27 (2017) - p. S129-S130 , 2017
Link:
https://doi.org/10.1016/..
?
2
Atypical phenotype of DMD carrier:
Haberlova, J.
;
Fajkusová, L.
;
Zámečník, J.
..
Neuromuscular Disorders. 26 (2016) - p. S125 , 2016
Link:
https://doi.org/10.1016/..
?
3
Ten years ofDNAdiagnostics of epidermolysis bullosa in the ..:
Kopečková, L.
;
Bučková, H.
;
Kýrová, J.
...
British Journal of Dermatology. 174 (2016) 6 - p. 1388-1391 , 2016
Link:
https://doi.org/10.1111/..
?
4
Functional analysis of mutations located in the LDL recepto..:
Freiberger, T.
;
Pavlouskova, J.
;
Reblova, K.
..
Atherosclerosis. 252 (2016) - p. e43 , 2016
Link:
https://doi.org/10.1016/..
?
5
Muscular dystrophies and myopathies: the spectrum of mutate..:
Stehlíková, K.
;
Skálová, D.
;
Zídková, J.
...
Clinical Genetics. 91 (2016) 3 - p. 463-469 , 2016
Link:
https://doi.org/10.1111/..
?
6
Diagnostic difficulties in muscular dystrophy due to LAMA2 ..:
Haberlová, J.
;
Barresi, R.
;
Fajkusová, L.
Neuromuscular Disorders. 25 (2015) - p. S269 , 2015
Link:
https://doi.org/10.1016/..
?
7
Autosomal recessive congenital ichthyoses in the Czech Repu..:
Bučková, H.
;
Nosková, H.
;
Borská, R.
...
British Journal of Dermatology. 174 (2015) 2 - p. 405-407 , 2015
Link:
https://doi.org/10.1111/..
?
8
The molecular basis of familial hypercholesterolemia in the..:
Tichy, L.
;
Freiberger, T.
;
Vrablik, M.
..
Atherosclerosis. 241 (2015) 1 - p. e114 , 2015
Link:
https://doi.org/10.1016/..
?
9
Fifteen years of active search for patients with familial h..:
Freiberger, T.
;
Fajkusova, L.
;
Tichy, L.
...
Atherosclerosis. 235 (2014) 2 - p. e197 , 2014
Link:
https://doi.org/10.1016/..
?
10
G.P.222:
Stehlikova, K.
;
Skalova, D.
;
Hruba, Z.
.
Neuromuscular Disorders. 24 (2014) 9-10 - p. 883 , 2014
Link:
https://doi.org/10.1016/..
?
11
G.P.99 Molecular genetic diagnostics of myotonia congenita ..:
Fajkusova, L.
;
Zı´dková, J.
;
Paclová, D.
...
Neuromuscular Disorders. 22 (2012) 9-10 - p. 898 , 2012
Link:
https://doi.org/10.1016/..
?
12
G.P.24 Congenital muscular dystrophy with epidermolysis bul..:
Mrazova, L.
;
Vondracek, P.
;
Buckova, H.
...
Neuromuscular Disorders. 22 (2012) 9-10 - p. 829-830 , 2012
Link:
https://doi.org/10.1016/..
?
13
Sequestration of MBNL1 in tissues of patients with myotonic..:
Lukáš, Z.
;
Falk, M.
;
Feit, J.
...
Neuromuscular Disorders. 22 (2012) 7 - p. 604-616 , 2012
Link:
https://doi.org/10.1016/..
?
14
G.P.44 Spectrum of mutations identified in the cohort of Cz..:
Hermanova, M.
;
Stehlikova, K.
;
Vondracek, P.
...
Neuromuscular Disorders. 22 (2012) 9-10 - p. 832 , 2012
Link:
https://doi.org/10.1016/..
?
15
P5.13 Spectrum of CLCN1 and SCN4A mutations in Czech patien..:
Fajkusova, L.
;
Paclova, D.
;
Sedlackova, J.
...
Neuromuscular Disorders. 21 (2011) 9-10 - p. 727 , 2011
Link:
https://doi.org/10.1016/..
1-15