Results 171 to 180 of about 181,370 (308)

Comparative Effectiveness and Safety of Inebilizumab Versus Rituximab in AQP4‐IgG‐Positive NMOSD

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Rituximab (anti‐CD20, RTX) and inebilizumab (anti‐CD19, INE) represent B‐cell‐depleting therapies used for aquaporin‐4 antibody‐positive (AQP4‐IgG+) neuromyelitis optica spectrum disorder (NMOSD); however, direct comparative evidence remains limited.
Jie Lin   +11 more
wiley   +1 more source

The landscape of gene mutations in a cohort of 3353 Han Chinese children with nonsyndromic hearing loss. [PDF]

open access: yesEBioMedicine
Xiao Y   +13 more
europepmc   +1 more source

CAR T‐Cell Therapy in Neurology: A Scoping Review of Neuro‐Oncology, Autoimmune Diseases & Neurotoxicity

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Chimeric antigen receptor (CAR) T‐cell therapy has been investigated in neurological diseases, encompassing both central nervous system malignancies and autoimmune disorders, thereby extending its application beyond hematological cancers.
Omar Alqaisi   +5 more
wiley   +1 more source

Martial arts fiction : translational migrations east and west [PDF]

open access: yes
This thesis was motivated by Robert Chard's puzzlement over the translational phenomenon of martial arts fiction in the West. It proposes to address how the translational migration of martial arts fiction took place, first to other Asian countries in ...
Mok, Olivia Wai Han
core  

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li   +11 more
wiley   +1 more source

Electrophysiological evidence of categorical perception of Chinese lexical tones in attentive condition

open access: yes, 2012
Previous electrophysiological evidence supports categorical perception of Chinese lexical tones at the preattentive stage (Xi and colleagues). In this study, we examined participants' attentive responses to tonal continua in an event-related potential ...
Zhang, Linjun   +5 more
core  

A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley   +1 more source

Maternal genetic structure and population affinities of the Sichuan Han Chinese based on whole mitochondrial genomes. [PDF]

open access: yesBMC Genomics
Jiang X   +12 more
europepmc   +1 more source

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