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JournalISSN: 0271-8235

Seminars in Neurology 

Thieme Medical Publishers (Germany)
About: Seminars in Neurology is an academic journal published by Thieme Medical Publishers (Germany). The journal publishes majorly in the area(s): Medicine & Stroke. It has an ISSN identifier of 0271-8235. Over the lifetime, 1948 publications have been published receiving 53050 citations.
Topics: Medicine, Stroke, Epilepsy, Disease, Poison control


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Journal ArticleDOI
TL;DR: Neglect is a failure to report, respond, or orient to contralateral stimuli that is not caused by an elemental sensorimotor deficit as mentioned in this paper, i.e., failure to respond, report or orient.
Abstract: Neglect is a failure to report, respond, or orient to contralateral stimuli that is not caused by an elemental sensorimotor deficit. Subtypes of neglect are distinguished by input (attentional) or output (intentional) demands, the distribution (personal, spatial, and representational), and the means of eliciting the signs (unilateral or bilateral stimuli). In this article we discuss how to assess patients for neglect, the pathophysiology of neglect, and the treatment of neglect.

1,879 citations

Journal ArticleDOI
TL;DR: Cognitive deficits believed to be a function of the severity of clinical sleep disturbance may be a product of genetic alleles associated with differential cognitive vulnerability to sleep loss.
Abstract: Deficits in daytime performance due to sleep loss are experienced universally and associated with a significant social, financial, and human cost. Microsleeps, sleep attacks, and lapses in cognition increase with sleep loss as a function of state instability. Sleep deprivation studies repeatedly show a variable (negative) impact on mood, cognitive performance, and motor function due to an increasing sleep propensity and destabilization of the wake state. Specific neurocognitive domains including executive attention, working memory, and divergent higher cognitive functions are particularly vulnerable to sleep loss. In humans, functional metabolic and neurophysiological studies demonstrate that neural systems involved in executive function (i.e., prefrontal cortex) are more susceptible to sleep deprivation in some individuals than others. Recent chronic partial sleep deprivation experiments, which more closely replicate sleep loss in society, demonstrate that profound neurocognitive deficits accumulate over time in the face of subjective adaptation to the sensation of sleepiness. Sleep deprivation associated with disease-related sleep fragmentation (i.e., sleep apnea and restless legs syndrome) also results in neurocognitive performance decrements similar to those seen in sleep restriction studies. Performance deficits associated with sleep disorders are often viewed as a simple function of disease severity; however, recent experiments suggest that individual vulnerability to sleep loss may play a more critical role than previously thought.

1,864 citations

Journal ArticleDOI
TL;DR: In high‐income countries mainly, improvements in prevention, acute treatment, and neurorehabilitation have led to a substantial decrease in the burden of stroke over the past 30 years.
Abstract: Stroke is the second leading cause of death and a major cause of disability worldwide. Its incidence is increasing because the population ages. In addition, more young people are affected by stroke in low- and middle-income countries. Ischemic stroke is more frequent but hemorrhagic stroke is responsible for more deaths and disability-adjusted life-years lost. Incidence and mortality of stroke differ between countries, geographical regions, and ethnic groups. In high-income countries mainly, improvements in prevention, acute treatment, and neurorehabilitation have led to a substantial decrease in the burden of stroke over the past 30 years. This article reviews the epidemiological and clinical data concerning stroke incidence and burden around the globe.

972 citations

Journal ArticleDOI
TL;DR: Advances in the field include improved methods of diagnosis, continued identification of disease genes, and the development of a unified model of pathogenesis in facioscapulohumeral dystrophy, which are reflected in thedevelopment of new therapeutic approaches.
Abstract: The muscular dystrophies are disorders of progressive muscular degeneration and weakness. As a group they display clinical heterogeneity that reflects the heterogeneity of molecular mechanisms responsible for them, and range from congenital to adulthood onset. Recent advances in the field include improved methods of diagnosis, continued identification of disease genes, and the development of a unified model of pathogenesis in facioscapulohumeral dystrophy. These advances are reflected in the development of new therapeutic approaches, some of which have already led to clinical trials in the dystrophinopathies and limb-girdle dystrophies.

752 citations

Performance
Metrics
No. of papers from the Journal in previous years
YearPapers
202332
202279
202164
202070
201957
201866