Zobrazeno 1 - 2
of 2
pro vyhledávání: '"S. V. Bugriy"'
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 12, Iss 1, Pp 51-58 (2020)
Aim. To consolidate literature data and to demonstrate rare hereditary neurogenetic syndromes with various neuropsychiatric manifestations and a corpus callosum (CC) structurally reduced in size.Material and methods. Full text data from scholarly jou
Externí odkaz:
https://doaj.org/article/a1473e69a9c340e692c08756e3d5f280
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 12, Iss 1, Pp 51-58 (2020)
Aim. To consolidate literature data and to demonstrate rare hereditary neurogenetic syndromes with various neuropsychiatric manifestations and a corpus callosum (CC) structurally reduced in size.Material and methods. Full text data from scholarly jou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93671e463a90818271ca82a12be18b0
https://doi.org/10.17749/2077-8333.2020.12.1.51-58
https://doi.org/10.17749/2077-8333.2020.12.1.51-58