Sleep Medicine
ISSN: 1389-9457
Datasets associated with articles published in Sleep Medicine
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11 results
- Data for: Patient experiences of sleep in dialysis: systematic review of qualitative studiesSystematic review and metanalysis of qualitative studies pertaining to the experiences of sleep in dialysis patients. Includes in-centre haemodialysis, peritoneal dialysis, home haemodialysis.
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- Data for: Autonomic dysfunction in childhood hypersomnia disorderspatients with hypersomnia may exhibit concurrent orthostatic intolerance that can contribute to daytime fatigue.
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- Data for: Sleep parameters assessed by actigraphy in Fabry's disease patients.The data presents valeus of sleep parameters.
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- Data for: Acute Post-stroke Restless Legs Syndrome:the body of caudate nucleus Considerations376 patients with acute cerebral infarction recruited from Tangshan gongren hosipital department of neurology between May 2016 and May 2017, were evaluated for RLS.
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- Data for: Short-interval intracortical inhibition is decreased in Restless Legs Syndrome across a range of severitydatabse sici, sba and rls
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- Data for: Effect of Insomnia after Acute Ischemic Stroke on Cerebrovascular Reactivity: A Prospective Clinical Study in ChinaThe upload file is the database of our manuscript.
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- Data for: Acute Post-stroke Restless Legs Syndrome:the body of caudate nucleus ConsiderationsSLEEP-D-19-00338
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- Data for: Association between total sleep time and all cancer mortality: Non-linear dose-response meta-analysis of cohort studiesThis is the detailed information for data extraction.
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- Dataset related to letter to editor "Epilepsy and NREM-parasomnia caused by novel hemizygous ARHGEF9 mutation"This dataset contains clinical and genetic information on the case described in the related Letter to editor
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- Dataset related to article "Epilepsy and NREM-parasomnia caused by novel hemizygous ARHGEF9 mutation"Descrizione: In 2012, we published the clinical case of a child with epilepsy and NREM-parasomnia of unknown cause. The boy, now aged 16 years old. In the suspicion of a genetic cause, the patient underwent to karyotype and CGH array that resulted unrevealing. 3-Tesla brain MRI was normal. Recently, the NGS analysis with a genetic panel for the screening of genes involved in epilepsy, identified the novel hemizygous missense variant c.1486G > A (p.Glu496Lys) in the X-linked ARHGEF9 gene (NM_015185.2, NP_056000.1)
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