Purpose: To investigate olfactory auras in patients with temporal lobe epilepsy (TLE).
Methods: We reviewed medical records of 217 Chinese patients who underwent temporal …

Objectives : The present study aimed to explore the role of microribonucleic acid (miRNA)
Let-7g in regulating endothelial functions. Background : Derangement of miRNAs is implicated …

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
(CADASIL) is originally featured with a strong clustering of mutations in NOTCH3 exons 3–…

Importance Transthyretin gene silencing is an emerging treatment strategy for hereditary
transthyretin (ATTRv) amyloidosis. Objective To evaluate eplontersen, an investigational ligand-…

Neuronal intranuclear inclusion disease (NIID), caused by an expansion of GGC repeats in
the 5′-untranslated region of NOTCH2NLC, is an important but underdiagnosed cause of …

Kawasaki disease (KD) is characterized by systemic vasculitis of unknown etiology. A study
from Japan reported that G to A substitution of a single-nucleotide polymorphism (SNP) …

Purpose: To investigate antiepileptic drug (AED) withdrawal during video‐EEG monitoring
in adult patients with temporal lobe epilepsy (TLE). Methods: Between 1995 and 1997, 102 …

Objective: To describe a novel mutation in TRK-fused gene (TFG) as a new cause of dominant
axonal Charcot-Marie-Tooth disease (CMT) identified by exome sequencing and further …

Background: Growing evidence suggests that white matter hyperintensities (WMHs) are
implicated in stroke recurrence and mortality, and their location can be a critical factor. This study …

Identification of genetic mutations has been of burgeoning importance in amyotrophic lateral
sclerosis (ALS) in recent years. The aim of this study was to determine the frequency and …