Results 51 to 60 of about 19,051 (305)

Shared decision making: A novel approach to personalized treatment in obstructive sleep apnea

open access: yesSleep Medicine: X, 2022
Study objectives: i) To describe a novel approach of phenotyping by shared decision making (SDM) in obstructive sleep apnea (OSA) discharge consultations ii) to describe correlation between patient and observer based evaluations of SDM and iii) to ...
Caroline Tonje Øverby   +4 more
doaj   +1 more source

Autoimmune Encephalitis in Acute Care—Pathology, Diagnosis, and Management

open access: yesAdvanced Science, EarlyView.
ABSTRACT Autoimmune encephalitis (AE) is characterized by immune‐mediated inflammation of the brain parenchyma, presenting with various neurological syndromes, including but not limited to seizures, altered consciousness, neuropsychiatric symptoms, and movement disorders.
Suneesh Thilak   +9 more
wiley   +1 more source

Multidimensional and Multifunctional Laser‐Induced Graphene (LIG) for Point‐of‐Care and Wearable Biosensing, Theranostics, and Bioactive Interfaces Toward Personalized Healthcare and Regenerative Medicine

open access: yesAdvanced Science, EarlyView.
Multidimensional laser‐induced graphene (LIG) spanning from 0D to 3D architectures is comprehensively reviewed for multifunctional biomedical platforms, including biosensing, theranostics, and bioactive interface applications, which highlights its potentials for point‐of‐care diagnostics, wearable health monitoring, smart drug delivery, and tissue ...
Li Zhang   +3 more
wiley   +1 more source

Hubungan Phantom Vibration Syndrome Terhadap Sleep Disorder dan Kondisi Stress

open access: yesJurnal Optimasi Sistem Industri, 2017
Phantom vibration syndrome is a condition where a person would feel the sensation of vibration of a cell phone as if there were incoming notification but the fact is not.
Ajeng Yeni Setianingrum
doaj   +1 more source

The 9th International RASopathies Symposium

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The RASopathies are a group of congenital disorders with overlapping clinical manifestations that are caused by pathogenic germline or early somatic variants that result in the hyperactivation of the RAS/mitogen‐activated protein kinase (MAPK) signaling pathway.
Pau Castel   +41 more
wiley   +1 more source

Central sleep apnea and hypoventilation syndromes

open access: yes, 2017
Sleep disordered breathing (SDB) may occur in a variety of ways. While obstructive sleep apnea is the most common of these, this chapter reviews the most common types of SDB that occur independently of upper airway obstruction.
Mithri R. Junna   +2 more
core   +1 more source

Sleep Apnea Syndrome in the Elderly [PDF]

open access: yesSleep, 1992
Sleep apnea syndrome (SAS) is a well established sleep disorder with high morbidity and mortality. Patients are most often middle-aged men. SAS occurs in at least 1% of the adult population. Several studies have suggested that SAS is extremely frequent in the elderly, its prevalence ranging from 18 to 73% in this group.
openaire   +2 more sources

A community-based study to estimate the burden and determinants of risk of developing obstructive sleep apnea among adults in an area of North India

open access: yesIndian Journal of Community and Family Medicine
Introduction: Obstructive sleep apnea (OSA) is an often underestimated sleep disorder that poses significant health risks among adults worldwide. This community-based cross-sectional study was undertaken to estimate the burden of risk of developing OSA ...
Garima Sangwan   +3 more
doaj   +1 more source

Polysomnographic features of children with obesity: body mass index predict severe obstructive sleep apnea in obese children? [PDF]

open access: yesClinical and Experimental Pediatrics
Background Few studies have explored the polysomnographic features of children with obesity. Purpose This study aimed to explore the demographic and polysomnographic features of obese children and determine whether body mass index (BMI) could predict ...
Rungrat Sukharom   +4 more
doaj   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet   +10 more
wiley   +1 more source

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