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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
Susie Kim,Kelsey Steffen,Lauren Gottschalk-Henneberry et al. Susie Kim et al.
Objective: Cerebral palsy (CP) is the most common lifelong motor disability worldwide. Yet, data is limited on how CP manifests in the US. Our objective was to characterize and determine factors affecting functional outco...
Chloë A Kerridge,Roberto S Hernandez,Nora C Hernandez et al. Chloë A Kerridge et al.
Objective: Essential tremor is a highly prevalent movement disorder. Pathological changes observed in essential tremor cerebella center around Purkinje cells and neighboring neuronal populations. Postmortem studies have v...
Wenci Yan,Terence Quinn,Alex McConnachie et al. Wenci Yan et al.
Objective: Cognitive decline can occur following ischaemic stroke. How cognition changes over time and associations with cognitive change are poorly understood. This study aimed to explore these issues over 2 years follow...
Giovanna S Manzano,Denis Balaban,Yihan Zhang et al. Giovanna S Manzano et al.
Objective: The optimal treatment for neurosarcoidosis myelitis is uncertain. We characterize incident neurosarcoidosis myelitis and assess treatment response by MRI and clinical scales. ...
Tatchaporn Ongphichetmetha,Mengke Du,Nisa Vorasoot et al. Tatchaporn Ongphichetmetha et al.
Clinicians often repeat aquaporin-4-immunoglobulin G (AQP4-IgG) testing in case of possible seroconversion. Compared with older, less sensitive immunofluorescence assays (IFA), cell-based assays (CBA) offer higher sensitivity. This study as...
Taru M Flagan,Stephanie A Chu,Suvi Häkkinen et al. Taru M Flagan et al.
Objective: Autosomal dominant progranulin (GRN) pathogenic variants are a genetic cause of frontotemporal lobar degeneration. Though clinical trials for GRN-related therapies are underway, there is an unmet need for bioma...
Zidan Gao,Zhuoma Danzhen,Yao Li et al. Zidan Gao et al.
Background: Olfactory dysfunction is frequently observed in patients with multiple sclerosis (MS); however, its underlying mechanisms remain poorly understood. To date, no studies have directly examined the nasal mucosal ...
Jiao-Jiao Xu,Yu-Lan Chen,Wan-Bing Sun et al. Jiao-Jiao Xu et al.
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 ...
Ellie McCluey,Ahmad A Toubasi,Jiacheng Wang et al. Ellie McCluey et al.
Background: The relationship between paramagnetic rim lesions (PRLs) and surrounding normally appearing white matter (NAWM) disease, potentially contributory to the associations seen between PRLs and clinical impairment, ...