166 - 180 of 183 Items
Is remission in women with idiopathic generalized epilepsy possible without valproate?
Kamil Wężyk, Agnieszka Słowik, Magdalena Bosak
Research Paper
Joanna Jędrzejczak, Beata Majkowska-Zwolińska
Research Paper
Małgorzata Dudzic, Anna Pieczyńska, Artur Drużdż, Katarzyna Hojan
Review Article
Whole exome sequencing-based testing of adult epilepsy in a Polish population
Magdalena Mroczek, Dominika Szczęśniak, Karolina Ziora-Jakutowicz, Magdalena Kacprzak, Paweł Aleksandrowicz, Małgorzata Bednarska-Makaruk, Lidia Kotuła
Short Communication
Carla Brenlla, Carlos Lazaro-Hernandez, Manel Fernandez, Jesica Perez-Montesino, Lorena de Mena, Nuria Bargallo, Veronica Sanchez, Andres Perissinotti, Aida Niñerola-Baizan, Alexandra Perez-Soriano, Celia Painous, Ana Cámara, Yaroslau Compta
Invited Review Article
Katarzyna Sawczyńska, Paweł Wrona, Kaja Zdrojewska, Dominik Wróbel, Kamil Wężyk, Paulina Sarba, Tadeusz Popiela, Agnieszka Słowik, Marcin Krzanowski
Research Paper
Innovations in epilepsy treatment: pharmacological strategies and machine learning applications
Natalia Chmielewska, Janusz Szyndler
Invited Review Article
Response to: DNAJC30 variants can also manifest phenotypically as Leigh/LHON overlap syndrome
Karol Chojnowski, Kamil Dzwilewski, Magdalena Krygier, Marta Zawadzka, Maria Mazurkiewicz-Bełdzińska
Response to Letter to the Editors
Konrad Kaleta, Kamil Możdżeń, Agnieszka Murawska, Żaneta Chatys-Bogacka, Karolina Porębska, Małgorzata Dec-Ćwiek
Response to Letter to the Editors
Differences in prevalence of orthostatic hypotension between Parkinson’s Disease motor subtypes
Panteleimon Oikonomou, Jiri Koschel, Christian F. Altmann, Wolfgang H. Jost
Letter to the Editors
Uncommon localised form of axonal injury involving pontes grisei caudatolenticulares
Francisca Sena Batista, Filipa Castelão, Carlos Casimiro, Lígia Neves, Denil Champac Tribovane
Letter to the Editors
CANVAS as example of genetic and clinical complexity of RFC1-related disorders
Filip Tomczuk, Anna Sulek, Piotr Janik
Invited Review Article
Family report of Birk-Barel syndrome — a neurodevelopmental channelopathy with epigenetic signature
Dorota Piekutowska-Abramczuk, Maria Jędrzejowska, Elżbieta Ciara, Dorota Jurkiewicz, Paulina Halat-Wolska, Marlena Młynek, Krystyna Chrzanowska, Rafał Płoski, Agnieszka Madej-Pilarczyk
Letter to the Editors
