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期刊名:Seminars in neurology

缩写:SEMIN NEUROL

ISSN:0271-8235

e-ISSN:1098-9021

IF/分区:2.0/Q3

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共收录本刊相关文章索引1253
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
Sarah Song Sarah Song
Stroke is a devastating disease and currently the fourth leading cause of death in this country. Acute ischemic stroke is an emergency and requires effective triage, diagnosis, and critical management. The hyperacute management of ischemic ...
Janice L Farlow,Tatiana Foroud Janice L Farlow
Over the past decade, there has been a dramatic evolution of genetic methodologies that can be used to identify genes contributing to disease. Initially, the focus was primarily on classical linkage analysis; more recently, genomewide assoc...
Shannon L Risacher,Andrew J Saykin Shannon L Risacher
Neurodegenerative disorders leading to dementia are common diseases that affect many older and some young adults. Neuroimaging methods are important tools for assessing and monitoring pathological brain changes associated with progressive n...
Dulanji K Kuruppu,Brandy R Matthews Dulanji K Kuruppu
Young-onset dementia is a neurologic syndrome that affects behavior and cognition of patients younger than 65 years of age. Although frequently misdiagnosed, a systematic approach, reliant upon attainment of a detailed medical history, a co...
Orna O&#x;Toole,Stacey Clardy,Amy May Lin Quek Orna O&#x;Toole
Immune-mediated encephalitis is an increasingly recognized cause of neurologic dysfunction including behavioral change, psychosis, movement disorders, seizures, autonomic instability, and coma. Associated antineuronal antibodies are of two ...
Leonel T Takada,Michael D Geschwind Leonel T Takada
Prion diseases are a group of diseases caused by abnormally conformed infectious proteins, called prions. They can be sporadic (Jakob-Creutzfeldt disease [JCD]), genetic (genetic JCD, Gerstmann-Sträussler-Scheinker, and familial fatal inso...
Youngsin Jung,Joseph R Duffy,Keith A Josephs Youngsin Jung
Primary progressive aphasia is a neurodegenerative syndrome characterized by progressive language dysfunction. The majority of primary progressive aphasia cases can be classified into three subtypes: nonfluent/agrammatic, semantic, and logo...
David C Perry,Bruce L Miller David C Perry
Frontotemporal dementia (FTD) encompasses several clinical syndromes that involve a progressive change in behavior and/or language; it is more common than Alzheimer's disease in early-onset dementia under the age of 60 years. In the behavio...