Results 1 to 10 of about 18,565 (309)

Autosomal Dominant Partial Epilepsies

Pediatric Neurology Briefs, 2000
The clinical, electrophysiologic, and genetic characteristics of autosomal dominant partial epilepsy were studied in 71 patients and 33 non-epileptic at-risk family members in 19 European families followed at the Hopital Universitaire de Geneve ...
J Gordon Millichap
doaj   +3 more sources

Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay [PDF]

Orphanet Journal of Rare Diseases
Background The SLC9A6 gene encodes a monovalent sodium-selective sodium/hydrogen exchanger that is essential in regulating endosomal PH and volume. SLC9A6 variants are associated with Christianson Syndrome, a severe neurodevelopmental disorder that is ...
Jun-Ping Jiao, Hong-Wei Zhang, Xi-Zhong Zhou, Shu-Juan Tian, Li Gao, Bing-Mei Li, Jun-Xia Luo, Jie Wang, Song Lan, Bin Li, Wei-Ping Liao   +10 more
doaj   +2 more sources

A clinical evaluation of gelastic and dacrystic seizures: a multicenter study

Arquivos de Neuro-Psiquiatria, 2022
Background Gelastic seizures are extremely rare, short-lasting, unprovoked, and uncontrollable laughing attacks. We conducted this retrospective evaluation to determine whether these symptoms, manifesting in different forms, such as cheerful laughter ...
Aylin Bican Demir, Başak Yılmaz Öz, Mustafa Onur Yıldız, Bengi Gül Türk, Taner Tanrıverdi, Ahmet Bekar, Naz Yeni, İbrahim Bora   +7 more
doaj   +1 more source

Nonketotic hyperglycemia with epileptic seizure: one case report

Chinese Journal of Contemporary Neurology and Neurosurgery, 2021
doi：10.3969/j.issn.1672⁃6731.2021.12 ...
GAO Yu⁃tian, LIU Wen⁃juan, WANG Ke⁃jian, HUANG Zuo⁃yi   +3 more
doaj   +1 more source

Electroclinical characteristics of MRI negative focal epilepsy: A video-EEG study [PDF]

Vojnosanitetski Pregled, 2020
Background/Aim. Epileptogenic lesions carry intrinsic epileptogenicity or epileptogenic potential in their close vicinity. One third of patients with focal epilepsy have no epileptogenic lesions magnetic resonance imaging [MRI(-)].
Ristić Aleksandar J., Arsić Aleksandra, Trajković Goran, Berisavac Ivana, Kisić Bojana   +4 more
doaj   +1 more source

Satisfying outcome of vagus nerve stimulation applied in the treatment of a patient with drug-resistant epilepsy caused by periventricular nodular heterotopia [PDF]

Vojnosanitetski Pregled, 2023
Introduction. Periventricular nodular heterotopia (PNH) is a developmental malformation of the cerebral cortex characterized by abnormal migration of neurons into the cortical plate and is often associated with drug-resistant focal epilepsy. Case report.
Todorović Stefan, Biševac Boban, Lukić Stevo, Ilić Jovan, Aleksić Dejan   +4 more
doaj   +1 more source

Aggravation of symptomatic occipital epilepsy of childhood by carbamazepine [PDF]

Vojnosanitetski Pregled, 2014
Introduction. Carbamazepine can lead to aggravation of epileptic seizures in generalized epilepsies (primary or secondary) with clinical manifestations of absence (typical or atypical) and/or myoclonic seizures.
Škrijelj Fadil E., Mulić Mersudin
doaj   +1 more source

Benign Partial Nonrolandic Epilepsies

Pediatric Neurology Briefs, 1991
The syndrome of benign partial epilepsy with particular reference to the non-rolandic types is described and the relevant literature reviewed from the Pediatric Seizure Clinic and EEG Laboratory, Beilinson Medical Center, Petah Tikva, and the Sackler ...
J Gordon Millichap
doaj   +1 more source

Inherited Epilepsies

Bezmiâlem Science, 2020
Mutations in genes encoding the formation of ion channels may cause epileptic syndromes. These epileptic syndromes are generally divided into generalized and partial epilepsies.
Halil Aziz VELİOĞLU, Muhammed Yunus BEKTAY   +1 more
doaj   +1 more source

Antiepileptic potential of ganaxolone [PDF]

Vojnosanitetski Pregled, 2017
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Janković Slobodan, Lukić Snežana
doaj   +1 more source