Results 221 to 230 of about 174,921 (327)
Automatic detection of hippocampal sclerosis in patients with epilepsy
Abstract Objective This study was undertaken to develop and validate an automatic, artificial intelligence‐enhanced software tool for hippocampal sclerosis (HS) detection, using a variety of standard magnetic resonance imaging (MRI) protocols from different MRI scanners for routine clinical practice.
Marcus Belke +14 more
wiley +1 more source
Associations of neurodegenerative and cerebrovascular neuropathology with frailty in a diverse sample. [PDF]
Bozi-Soares F +9 more
europepmc +1 more source
Topiramate for the treatment of neonatal seizures and beyond
Abstract Acute symptomatic neonatal seizures are one of the most common neurological disorders in newborns admitted to neonatal intensive care units and require prompt treatment. Up to 50% of neonatal seizures are refractory to first‐line medications such as phenobarbital (PB), and another 30% fail second‐line therapy.
Wolfgang Löscher, Janet S. Soul
wiley +1 more source
NEUROPATHOLOGY AND FORENSIC PATHOLOGY: TWO VIEWPOINTS [PDF]
William F. McCormick
openalex +1 more source
The emergence of network inefficiencies in infants with autism spectrum disorder [PDF]
Botteron, Kelly N +3 more
core +1 more source
Abstract Objective Studies in temporal lobe epilepsy (TLE) have shown that focal inflammation is a key contributor to seizure initiation and maintenance. However, most in vivo studies to date have focused on positron emission tomography (PET) findings. In this exploratory study, we assessed the relationship between multicompartment Neurite Orientation ...
Jerzy P. Szaflarski +6 more
wiley +1 more source
A malignant choroid plexus tumor with heterologous differentiation and BAP1 deletion suggesting choroid plexus blastoma. [PDF]
Tauziède-Espariat A +9 more
europepmc +1 more source
Novel neuropathological observations in an adult with Dravet syndrome
Abstract Dravet syndrome (DS) is a developmental and epileptic encephalopathy associated with pathogenic variants in the SCN1A gene. The neuropathological features of adult DS remain poorly understood. We report the postmortem findings of a 55‐year‐old woman with DS due to a confirmed SCN1A pathogenic variant leading to Nav1.1 loss of function ...
Danielle M. Andrade +7 more
wiley +1 more source

