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Advanced Search Results For "RC321-571"

1 - 10 of 108,909 results for
 "RC321-571"
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HIV, HSV, SARS-CoV-2 and Ebola Share Long-Term Neuropsychiatric Sequelae

Publication Type:Academic Journal

Source(s):Neuropsychiatric Disease and Treatment, Vol Volume 18, Pp 2229-2237 (2022)

Abstract:Pascal Büttiker,1 George B Stefano,1 Simon Weissenberger,2 Radek Ptacek,1 Martin Anders,1 Jiri Raboch,1 Richard M Kream1 1Department of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech R...

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Ventriculosubgaleal shunting for spontaneous intraventricular haemorrhage: is it a good alternative to external ventricular drainage?

Publication Type:Academic Journal

Source(s):The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 58, Iss 1, Pp 1-8 (2022)

Abstract:Abstract Background Spontaneous intraventricular haemorrhage (IVH) is a life-threatening condition associated with high morbidity and mortality and is conventionally managed using external ventricular drain (EVD). However, EVD is commonly associated wi...

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Post-COVID isolated subclavian artery dissection with multiple cerebral infarctions

Publication Type:Academic Journal

Source(s):The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 58, Iss 1, Pp 1-5 (2022)

Abstract:Abstract Background Coronavirus disease 2019 (COVID-19) is a pandemic disease which predominantly affects the respiratory system with high critical care mortality and morbidity, yet it also causes multiple organs dysfunction in affected patients. There...

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The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8

Publication Type:Academic Journal

Source(s):Translational Psychiatry, Vol 12, Iss 1, Pp 1-11 (2022)

Abstract:Abstract CHD8, a major autism gene, functions in chromatin remodelling and has various roles involving several biological pathways. Therefore, unsurprisingly, previous studies have shown that intellectual developmental disorder with autism and macrocep...

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Exploring the causal effects of genetic liability to ADHD and Autism on Alzheimer’s disease

Publication Type:Academic Journal

Source(s):Translational Psychiatry, Vol 12, Iss 1, Pp 1-7 (2022)

Abstract:Abstract Few studies suggest possible links between attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD) and Alzheimer’s disease but they have been limited by small sample sizes, diagnostic and recall bias. We used two-sample...

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Structural stigma and its impact on healthcare for borderline personality disorder: a scoping review

Publication Type:Academic Journal

Source(s):International Journal of Mental Health Systems, Vol 16, Iss 1, Pp 1-41 (2022)

Abstract:Abstract Background People with Borderline Personality Disorder (BPD) and their carers/families continue to experience structural stigma when accessing health services. Structural stigma involves societal-level conditions, cultural norms, and organizat...

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Guillain–Barré syndrome variants: a grave complication of bariatric surgery

Publication Type:Academic Journal

Source(s):The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 58, Iss 1, Pp 1-4 (2022)

Abstract:Abstract Background Guillain–Barré syndrome is an acquired inflammatory disease of the peripheral nervous system. It is the most frequent cause of acute flaccid symmetrical weakness of the limbs and areflexia usually reaching its peak within a month. C...

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Long-term follow-up of telehealth-enabled behavioral treatment for challenging behaviors in boys with fragile X syndrome

Publication Type:Academic Journal

Source(s):Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-13 (2022)

Abstract:Abstract Background A significant proportion of boys with fragile X syndrome (FXS), the most common known genetic cause of intellectual disability, exhibit challenging behaviors such as aggression and self-injury that can cause significant distress to ...

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Baclofen-associated neurophysiologic target engagement across species in fragile X syndrome

Publication Type:Academic Journal

Source(s):Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-15 (2022)

Abstract:Abstract Background Fragile X syndrome (FXS) is the most common inherited form of neurodevelopmental disability. It is often characterized, especially in males, by intellectual disability, anxiety, repetitive behavior, social communication deficits, de...

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The impact of apraxia and neglect on early rehabilitation outcome after stroke

Publication Type:Academic Journal

Source(s):Neurological Research and Practice, Vol 4, Iss 1, Pp 1-11 (2022)

Abstract:Abstract Background This study aims to characterize the impact of apraxia and visuospatial neglect on stroke patients’ cognitive and functional outcomes during early rehabilitation. Prior work implies an unfavorable effect of visuospatial neglect on re...

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