Случаи фармакорезистентной эпилепсии при хромосомной патологииNovikova, L.B.,
Akopyan, A.P.,
Latypova, R.F.,
Faizullina, N.M.,
Л.Б. Новикова,
А.П. Акопян,
Р.Ф. Латыпова,
Н.М. Файзуллина (2024) mutation caused deletion of chromosome 14 are presented. In the
first case, this pathology was manifested
Khamidullina, Zemfira,
Avzaletdinova, Diana,
Gareeva, Diana,
Morugova, Tatyana,
Lakman, Irina,
Kopp, Kristen,
Fiedler, Lukas,
Motloch, Lukas J.,
Zagidullin, Naufal (2024) : A total of 2486 hospitalized patients in the
first wave of COVID-19 were analyzed according
Akhkiamova, Maria,
Polyakov, Aleksander,
Marakhonov, Andrey,
Voronin, Sergey,
Saifullina, Elena,
Vafina, Zulfiia,
Michalchuk, Kristina,
Braslavskaya, Svetlana,
Chukhrova, Alena,
Ryadninskaya, Nina,
Kutsev, Sergey,
Shchagina, Olga (2024) atrophy (5q SMA). Within the 253-sample risk group formed based on the results of the
first screening