Results 241 to 250 of about 8,448,369 (354)
Accelerated Progression of Gait Impairment in Parkinson's Disease and REM Sleep Without Atonia
ABSTRACT Objective People with Parkinson's disease (PD) and rapid eye movement (REM) sleep without atonia (RSWA) often have more severe gait disturbances compared to PD without RSWA. The association between the presence and expression of RSWA and the rate of progression of gait impairment in PD is unknown.
Sommer L. Amundsen‐Huffmaster +11 more
wiley +1 more source
The psychological and behavioral effects of social isolation on mass shooters. [PDF]
Lankford A, Silva JR.
europepmc +1 more source
ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando +13 more
wiley +1 more source
Social Isolation and Mortality in Older Adults in Sweden: A Cohort Study. [PDF]
Wolde S, Miao Jonasson J.
europepmc +1 more source
Turnover Intention, Emotional Exhaustion, Perceived Social Support, and Professional Isolation among Special Educators and Regular Teachers [PDF]
Gopal Krishna, Rashmi Rangaswamy
openalex +1 more source
Decreased Serum 5‐HT: Clinical Correlates and Regulatory Role in NMJ of MG
ABSTRACT Objective Although 5‐Hydroxytryptamine (5‐HT) indirectly stimulates muscle contraction and participates in regulating Acetylcholine receptor (AChR) cluster homeostasis in cellular, animal, and clinical studies, evidence regarding its potential to modulate muscle contraction in myasthenia gravis (MG) remains limited.
Xinru Shen +18 more
wiley +1 more source
Global Trends and Disparities in Social Isolation.
Fuller-Rowell TE, Sultana S, Kawachi I.
europepmc +1 more source
Viewing social isolation as a complex dynamical system: A theoretical and computational framework. [PDF]
Abplanalp SJ, Maimone JS, Green MF.
europepmc +1 more source
Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay in Two Half‐Siblings
ABSTRACT Autosomal recessive spastic ataxia of Charlevoix‐Saguenay (ARSACS) is caused by biallelic pathogenic variants in the SACS gene. We report the clinical, radiologic and neurophysiologic features of a pair of half‐siblings who presented with progressive cerebellar ataxia, peripheral neuropathy and upper motor neuron signs.
Dennis Yeow +6 more
wiley +1 more source

