Xanthine Oxidoreductase: A Double-Edged Sword in Neurological Diseases. [PDF]
Bortolotti M +3 more
europepmc +1 more source
Decreased Serum 5‐HT: Clinical Correlates and Regulatory Role in NMJ of MG
ABSTRACT Objective Although 5‐Hydroxytryptamine (5‐HT) indirectly stimulates muscle contraction and participates in regulating Acetylcholine receptor (AChR) cluster homeostasis in cellular, animal, and clinical studies, evidence regarding its potential to modulate muscle contraction in myasthenia gravis (MG) remains limited.
Xinru Shen +18 more
wiley +1 more source
CAR T-cells meet autoimmune neurological diseases: a new dawn for therapy. [PDF]
Chinas NA, Alexopoulos H.
europepmc +1 more source
Clinical Characteristics and Outcomes of Early‐Onset Versus Late‐Onset LGI1‐Antibody Encephalitis
ABSTRACT Background Leucine‐rich glioma‐inactivated 1 antibody (LGI1‐Ab) encephalitis predominantly affected older individuals, but has also been reported in younger patients. However, the demographic, clinical, and prognostic characteristics of early‐onset LGI1‐Ab encephalitis have yet to be systematically elucidated. This study aims to systematically
Yu Kong +7 more
wiley +1 more source
Editorial: Drug discovery from herbal medicines/polypeptides for neurological diseases. [PDF]
Liang Q, Zhang J, Lin L, Wang J.
europepmc +1 more source
ABSTRACT Background Apolipoprotein ε4 (APOE ε4) is a potent genetic risk factor for Alzheimer's disease (AD). However, its role in cerebral small vessel disease (CSVD) remains unclear. Given the clinical and pathological similarities between CSVD and AD, this study aimed to investigate the associations of APOE ε4 gene dosage with cognitive function and
Tingru Jin +6 more
wiley +1 more source
The application of radiomics in the diagnosis and evaluation of cognitive impairment related to neurological diseases. [PDF]
Xiao H +5 more
europepmc +1 more source
RAB39B Related Parkinsonism in an Italian Family: A Unique Use of Advanced Therapies
ABSTRACT Parkinson's disease (PD) is a neurodegenerative disorder that may sometimes be caused by deleterious genetic variants. Among them, RAB39B polymorphisms are known as rare causes of early‐onset PD associated with intellectual disability (Waisman's syndrome).
Caterina Del Regno +13 more
wiley +1 more source
Correction to "The Impact of SETBP1 Mutations in Neurological Diseases and Cancer". [PDF]
europepmc +1 more source
Single-cell transcriptomics for immune profiling of cerebrospinal fluid in neurological diseases. [PDF]
Ramos-Vicente D +5 more
europepmc +1 more source

