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期刊名:Annals of clinical and translational neurology

缩写:ANN CLIN TRANSL NEUR

ISSN:2328-9503

e-ISSN:2328-9503

IF/分区:3.9/Q1

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共收录本刊相关文章索引2423
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Zhiqiang Xu,Xiaoxiao Wang,Nan Li Zhiqiang Xu
Objectives: This study aimed to examine the relationship between the McCance Brain Care Score (BCS) and mortality in the general population. Methods: ...
Erik Fernström,Thomas Björk-Eriksson,Pontus Erickson et al. Erik Fernström et al.
In this study, we analyzed biomarkers of neuronal, glial, and vascular injury in longitudinal paired samples of blood and cerebrospinal fluid after prophylactic cranial irradiation in patients with small cell lung cancer. Neurofilament ligh...
Daniel Chelsky,Cara Joyce,H Jeremy Bockholt et al. Daniel Chelsky et al.
Objective: Clinical trials for Huntington's disease (HD) enrolling persons before clinical motor diagnosis (CMD) lack validated biomarkers. This study aimed to conduct an unbiased discovery analysis and a targeted examina...
Tuhin Virmani,Lakshmi Pillai,Reid D Landes et al. Tuhin Virmani et al.
Objective: Freezing of gait (FOG) in people with Parkinson's disease (PwPD) is debilitating and has limited treatments. Modafinil modulates beta/gamma band activity in the pedunculopontine nucleus (PPN), like PPN deep bra...
Dennis Yeow,Matthew Katz,Jonathan Rodgers et al. Dennis Yeow et al.
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is caused by biallelic pathogenic variants in the SACS gene. We report the clinical, radiologic and neurophysiologic features of a pair of half-siblings who presented with p...
Vrishab Commuri,Isabella Dallasta,Ciaran Stone et al. Vrishab Commuri et al.
Objective: Patients with minor stroke exhibit slowed processing speed and generalized alterations in functional connectivity involving frontoparietal cortex (FPC). The pattern of connectivity evolves over time. In this st...
Yeting Luo,Shuhua Xie,Xianghong Liu Yeting Luo
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a chronic autoimmune neuroinflammatory disease, typically characterized by antibodies against aquaporin 4 (AQP4-IgG) or myelin oligodendrocyte glycoprotein (MOG-IgG). Simultaneous seropositi...
Amin Mehrabian,Peter Auguste,Amy Grove et al. Amin Mehrabian et al.
Objective: Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring co...
Mengxuan Tang,Amerta Bai,Felipe Rodridgues Marques Ferreira et al. Mengxuan Tang et al.
New-onset refractory status epilepticus (NORSE) arises without an identifiable cause or prior epilepsy history, with a 16%-27% mortality rate and significant long-term neurological sequelae. Neuromodulation such as deep brain stimulation (D...
Sam G Norwitz,Josefine Eck,Joel S Winston et al. Sam G Norwitz et al.
Objectives: We describe the clinical manifestations and developmental abilities of individuals with SYT1-associated neurodevelopmental disorder (Baker-Gordon syndrome) from infancy to adulthood. We further describe the ne...