Results 61 to 70 of about 589,280 (296)

Nonepileptic Seizures

Neurologic Clinics, 1995
The widespread use of video-electroencephalogram monitoring has dramatically increased our recognition of the high prevalence and diversity of nonepileptic seizures. Nonepileptic seizures stand squarely in the interface between psychiatry and neurology, an area that has been both claimed and denied by both sides.
O, Devinsky, K, Thacker
openaire   +2 more sources

Financial Burden Associated With Hospitalisation Among Families of Childhood Brain Tumours in Australia

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Families of children with cancer experience significant financial strain, even with universal healthcare. Indirect costs, such as productivity losses and non‐medical expenses, are rarely included in economic evaluations, and little is known about how effectively financial aid programmes alleviate this burden. Childhood brain tumours
Megumi Lim, Natalie Bradford, David Brain, Sameera Senanayake, Sanjeewa Kularatna, Kate Young, Christine Cashion, Tim Hassall, Susanna Cramb   +8 more
wiley   +1 more source

Effect of Hydroalcoholic Extract of Stachys lavandulifolia on Pentylenetetrazole-induced Seizures in Male Mice: The Role of GABAergic and Opioidergic Systems

Basic and Clinical Neuroscience, 2022
Introduction: Epilepsy is one of the most common neurological disorders. Though there are several effective drugs for treating epilepsy, most drugs are associated with side effects and drug interactions. Stachys lavandulifolia used in Iranian traditional
Hamid Behzadnia, Amin Naseri, Mohammadreza Emamhadi, Shervin Ghadarjani, Iraj Aghaei, Ahmadreza Dehpour   +5 more
doaj  

A Rare Cause of Reversible Splenial Lesion Syndrome (RESLES): Benign Convulsions with Mild Gastroenteritis

Journal of Pediatric Research, 2021
Transient lesions involving the splenium of corpus callosum is defined as reversible splenial lesion syndrome (RESLES). Benign convulsions with mild gastroenteritis is a rare condition which may be associated with RESLES. Since the prognosis is excellent,
Nida Uysal, Afshin Dezhakam, Seda Kanmaz, Sanem Yılmaz   +3 more
doaj   +1 more source

The Fate (Outcome) of Clinically Apparent Single Lesion and Oligofocal Nephroblastomatosis Treated According to SIOP/GPOH Protocols for Wilms Tumor

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background The management of clinically apparent single lesions or oligofocal nephroblastomatosis, a facultative precursor of nephroblastoma, remains debated. Methods We retrospectively analyzed 37 patients with clinically apparent single or oligofocal nephroblastomatosis (two to three lesions per kidney) among 2347 patients registered between
Nils Welter, Jens‐Peter Schenk, Jenny Wegert, Manfred Gessler, Leo Kager, Stefan Wagenpfeil, Marina Müller, Jean‐Michel Wolff, Joerg Fuchs, Steven W. Warmann, Clemens‐Magnus Meier, Jochen Hubertus, Christian Rübe, Christian Vokuhl, Patrick Melchior, Lena Tschirner, Norbert Graf, Rhoikos Furtwängler   +17 more
wiley   +1 more source

Investigation of Behaviors of the Epilepsy Patients’ Relatives During Seizure and its Association with Their Knowledge Regarding Epilepsy

Archives of Epilepsy, 2021
Objectives:Relatives of epilepsy patients tend to intervene their patients during epileptic seizure with an intention to help them. Usually not based on a medical knowledge, these behaviors may harm the patient rather than providing benefit.
Zerin ÖZAYDIN AKSUN, Aytaç YİĞİT
doaj   +1 more source

A New Approach to Automated Epileptic Diagnosis Using EEG and Probabilistic Neural Network

, 2008
Epilepsy is one of the most common neurological disorders that greatly impair patient' daily lives. Traditional epileptic diagnosis relies on tedious visual screening by neurologists from lengthy EEG recording that requires the presence of seizure (ictal)
Bao, Forrest Sheng, Lie, Donald Yu-Chun, Zhang, Yuanlin   +2 more
core   +1 more source

EEG source connectivity to localize the seizure onset zone in patients with drug resistant epilepsy [PDF]

, 2017
Visual inspection of the EEG to determine the seizure onset zone (SOZ) in the context of the presurgical evaluation in epilepsy is time-consuming and often challenging or impossible.
Boon, Paul, Carrette, Evelien, Gadeyne, Stefanie, Keereman, Vincent, Meurs, Alfred, Momjian, Shahan, Pittau, Francesca, Seeck, Margitta, Staljanssens, Willeke, Strobbe, Gregor, Van Holen, Roel, van Mierlo, Pieter, Vandenberghe, Stefaan, Vonck, Kristl, Vulliémoz, Serge   +14 more
core   +5 more sources

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan, Lydie Da Costa, Ludivine David Nguyen, Heloise Chosseler, Audrey Riquet, Benedicte Bruno, Melissa Barbati   +6 more
wiley   +1 more source

Febrile Seizures

Don't Forget The Bubbles, 2014
Febrile seizure (FS) is the most common seizure disorder of childhood, and occurs in an age-related manner. FS are classified into simple and complex. FS has a multifactorial inheritance, suggesting that both genetic and environmental factors are causative. Various animal models have elucidated the pathophysiological mechanisms of FS.
openaire   +4 more sources