Exploring the diagnostic potential: magnetic particle imaging for brain diseases. [PDF]
Guo LS+8 more
europepmc +1 more source
Prenarcotic Doses of Barbiturates as an Aid in Localizing Diseased Brain Tissue [PDF]
Mary A. B. Brazier
openalex +1 more source
ABSTRACT Background Managing long COVID in people with multiple sclerosis and related disorders (pwMSRD) is complex due to overlapping symptoms. To address evidence gaps, we evaluated long COVID susceptibility in pwMSRD versus controls and its associations with multi‐domain function and disability.
Chen Hu+15 more
wiley +1 more source
Novel insights into the relationship between glaucoma and brain diseases from the genetic to diseases levels: A cross-sectional study. [PDF]
Chen X, Shi C, He M, Xia X.
europepmc +1 more source
Analysis of Soluble Interleukin‐2 Receptor as a Prognostic Biomarker in NMOSD and MOGAD
ABSTRACT Objective Soluble interleukin‐2 receptor (sIL‐2R) is a biomarker for T cell activity. T cells are involved in neuromyelitis optica spectrum disorders (NMOSD) and myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) pathogenesis. However, sIL‐2R has so far not been evaluated in these conditions.
Philipp Klyscz+8 more
wiley +1 more source
MR-Guidance of Gene Therapy for Brain Diseases: Moving From Palliative Treatment to Cures. [PDF]
Bermudez DH, Lilieholm T, Block WF.
europepmc +1 more source
Nerve Excitability in Asymptomatic Carriers and Amyotrophic Lateral Sclerosis Patients With C9orf72
ABSTRACT Objective We investigated the effects of C9orf72 mutation carriership on peripheral nerve excitability in asymptomatic individuals from families with a history of C9orf72 amyotrophic lateral sclerosis (ALS) and patients. Methods We included 47 asymptomatic individuals from families with a history of C9orf72 ALS, of whom 23 were carriers (C9 ...
Diederik J. L. Stikvoort García+3 more
wiley +1 more source
Investigation of the role of miRNA variants in neurodegenerative brain diseases. [PDF]
Frydas A+4 more
europepmc +1 more source
ABSTRACT Objective Paroxysmal kinesigenic dyskinesia (PKD) is the most common hereditary paroxysmal movement disorder. The PRRT2 gene is the first identified causative gene and accounts for the majority of PKD. In this study, we investigated the pathogenicity of PRRT2 variants in the splice regions. Methods Patients with clinically suspected PKD and no
Jiao‐Jiao Xu+5 more
wiley +1 more source
A realistic human head phantom for electromagnetic detection of brain diseases. [PDF]
Bai Z+7 more
europepmc +1 more source