Zobrazeno 1 - 10
of 311
pro vyhledávání: '"Julie C. Stout"'
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 4, Pp 989-999 (2024)
Abstract Objective Huntington's disease (HD) is an inherited neurodegenerative disease involving progressive motor abnormalities, cognitive decline, and psychiatric disturbances. Depression and cognitive difficulties are among the most impactful symp
Externí odkaz:
https://doaj.org/article/871d1e7b69a6439a97efe08a56f4b870
Autor:
Sophie C. Andrews, Lydia Kämpf, Dylan Curtin, Mark Hinder, Nicole Wenderoth, Julie C. Stout, James P. Coxon
Publikováno v:
Frontiers in Psychology, Vol 14 (2023)
IntroductionCardiorespiratory exercise has emerged as a promising candidate to modify disease progression in Huntington’s disease (HD). In animal models, exercise has been found to alter biomarkers of neuroplasticity and delay evidence of disease,
Externí odkaz:
https://doaj.org/article/75e69fc47fc046d9be4cce78f52d7f9e
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Huntington’s disease (HD) mouse models suggest that cardiovascular exercise may enhance neuroplasticity and delay disease signs, however, the effects of exercise on neuroplasticity in people with HD are unknown. Using a repeated-measures e
Externí odkaz:
https://doaj.org/article/dc899624c21f42869b3faac61925cc4d
Autor:
Rangi Kandane-Rathnayake, Eric F Morand, Vera Golder, Alberta Hoi, Sudha Raghunath, Julie C Stout, Yifat Glikmann-Johnston
Publikováno v:
Lupus Science and Medicine, Vol 10, Iss 1 (2023)
Objective Cognitive dysfunction in SLE is common, but clinical risk factors are poorly understood. This study aims to explore the associations of cognitive dysfunction in SLE with disease activity, organ damage, biomarkers and medications.Methods We
Externí odkaz:
https://doaj.org/article/01ff2de5a4784d0e83319c954bdd3804
Autor:
Daisy Abreu, Jennifer Ware, Nellie Georgiou-Karistianis, Blair R. Leavitt, Cheryl J. Fitzer-Attas, Raquel Lobo, Ana Raquel Fernandes, Olivia Handley, Karen E. Anderson, Julie C. Stout, Cristina Sampaio
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Introduction: An understanding of the clinimetric properties of clinical assessments, including their constraints, is critical to sound clinical study and trial design. Utilizing data from Enroll-HD—a global, prospective HD observational study and
Externí odkaz:
https://doaj.org/article/4af292b6ce0a4ba7b3b03db1ac9ee739
Autor:
Cory I. Wasser, Emily-Clare Mercieca, Geraldine Kong, Anthony J. Hannan, Brianna Allford, Sonja J. McKeown, Julie C. Stout, Yifat Glikmann-Johnston
Publikováno v:
Journal of Huntington's Disease. 12:43-55
Background: Gastrointestinal symptoms are clinical features of Huntington’s disease (HD), which adversely affect people’s quality of life. We recently reported the first evidence of gut dysbiosis in HD gene expansion carriers (HDGECs). Here, we r
The temporal dynamics of mood and their association with depressive symptoms in Huntington's disease
Publikováno v:
Journal of Affective Disorders. 328:22-28
Autor:
Sudha Raghunath, Yifat Glikmann-Johnston, Fabien B. Vincent, Eric F. Morand, Julie C. Stout, Alberta Hoi
Publikováno v:
Journal of the International Neuropsychological Society. 29:421-430
Objective:Systemic lupus erythematosus (SLE) is a chronic autoimmune disease, in which cognitive dysfunction is common, but poorly understood. This study aims to characterize the prevalence and patterns of cognitive dysfunction in SLE.Method:SLE pati
Autor:
Catherine Ding, Colin J. Palmer, Jakob Hohwy, George J. Youssef, Bryan Paton, Naotsugu Tsuchiya, Julie C. Stout, Dominic Thyagarajan
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Abstract Parkinson’s disease (PD) alters cortico-basal ganglia-thalamic circuitry and susceptibility to an illusion of bodily awareness, the Rubber Hand Illusion (RHI). Bodily awareness is thought to result from multisensory integration in a predom
Externí odkaz:
https://doaj.org/article/78d90c15958f48bd8873436cbc00cdae
Autor:
Lora Minkova, Sarah Gregory, Rachael I. Scahill, Ahmed Abdulkadir, Christoph P. Kaller, Jessica Peter, Jeffrey D. Long, Julie C. Stout, Ralf Reilmann, Raymund A. Roos, Alexandra Durr, Blair R. Leavitt, Sarah J. Tabrizi, Stefan Klöppel
Publikováno v:
NeuroImage: Clinical, Vol 17, Iss , Pp 312-324 (2018)
Huntington's disease (HD) is a progressive neurodegenerative disorder that can be genetically confirmed with certainty decades before clinical onset. This allows the investigation of functional and structural changes in HD many years prior to disease
Externí odkaz:
https://doaj.org/article/b4308c9929ef4302b37f33f5c7d08710