Results 141 to 150 of about 57,981 (292)
Neurologic manifestations in children with COVID-19. [PDF]
Gürlevik SL +8 more
europepmc +1 more source
ABSTRACT Paramagnetic rim lesions (PRLs) and choroid plexus (CP) enlargement reflect smoldering inflammation in multiple sclerosis. Their role in cognitive progression remains unexplored. Eighty‐seven early relapsing–remitting MS patients were enrolled at diagnosis and followed longitudinally.
Stefano Ziccardi +15 more
wiley +1 more source
Neurologic Manifestations of Long COVID Differ Based on Acute COVID-19 Severity. [PDF]
Perez Giraldo GS +33 more
europepmc +1 more source
Human Pegivirus Encephalitis With Brain Detection and Response to Sofosbuvir Ledipasvir
ABSTRACT Human pegivirus (HPgV‐1) has been associated with severe encephalomyelitis in immunocompromised patients. Its neurological spectrum remains poorly defined. We report a slowly progressive encephalitis in a person living with well‐controlled HIV, characterized by white matter abnormalities and inflammatory cerebrospinal fluid (CSF). HPgV RNA was
Antoine Moulignier +3 more
wiley +1 more source
Therapeutic Approaches to the Neurologic Manifestations of COVID-19. [PDF]
Graham EL, Koralnik IJ, Liotta EM.
europepmc +1 more source
ABSTRACT Objectives Focal cortical dysplasia (FCD) is the most common etiology of drug‐resistant epilepsy in children. Focal to bilateral tonic–clonic seizures (FBTCS) mark a high risk of drug‐resistant epilepsy and involve thalamocortical circuitry in their generation and propagation.
Hua Xie +8 more
wiley +1 more source
Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based Study. [PDF]
Haji Esmaeil Memar E +20 more
europepmc +1 more source
A 57‐Year‐Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations
ABSTRACT This report presents a case of behavioral variant frontotemporal dementia caused by mutations in the MATR3 and NOS3 genes, aiming to analyze its clinical manifestations and genetic characteristics. For a case presenting with personality changes and gait abnormalities as the initial symptoms, this study conducted a comprehensive analysis of its
Feifei Lin, Saie Huang
wiley +1 more source
Background:Wilson’s disease (WD) is an inherited disorder of copper metabolism that is characterized by tremendous variation in the clinical presentation.
Ahmed Kh . Mohammed +2 more
doaj
COVID-19 and neurologic manifestations: a synthesis from the child neurologist's corner. [PDF]
Valderas C +5 more
europepmc +1 more source

