Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hana, Oslejskova"'
Autor:
Jana POKORNA, Zdenka BALINTOVA, Vladan BERNARD, Erik STAFFA, Vojtech MORNSTEIN, Hana OSLEJSKOVA
Publikováno v:
Bratislava Medical Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcd23406c7a4b3171c402b81f98219a8
https://doi.org/10.4149/bll_2023_090
https://doi.org/10.4149/bll_2023_090
Autor:
Katarina, Ceska, Pavlina, Danhofer, Ondrej, Horak, Klara, Spanelova, Senad, Kolar, Hana, Oslejskova, Stefania, Aulicka
Publikováno v:
Bratislava Medical Journal. 123:483-486
with the Dravet's syndrome phenotype are associated with the detection of a sequence variant in the SCN1A gene (alpha 1 subunit of the voltage-gated sodium channel) (2). However, sequence variants in the SCN1A gene are associated with a very broad cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68aa01a0d058f2f3ff4660f3670cf6e4
https://doi.org/10.4149/bll_2022_076
https://doi.org/10.4149/bll_2022_076
Publikováno v:
Epileptic disorders : international epilepsy journal with videotape. 9
The aim of this study was to categorize speech problems in autistic children in a manner allowing recognition of associated risk factors. We were specifically interested in the role of epilepsy and epileptiform activity in EEG in autistic patients si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4943ca34130e6da516fa2165c158ffcf
https://pubmed.ncbi.nlm.nih.gov/18319196
https://pubmed.ncbi.nlm.nih.gov/18319196