Search Results - "Masellis, Mario"

Genetic variation in the dopamine system is associated with mixed‐strategy decision‐making in patients with Parkinson's disease.

Authors: Parr, Ashley C. Riek, Heidi C. Coe, Brian C. et al.

Source: European Journal of Neuroscience. Dec2023, Vol. 58 Issue 12, p4523-4544. 22p.

Subjects: Dopamine, Parkinson's disease, Genetic variation, Genetic profile, Single nucleotide polymorphisms, Reinforcement learning

A Cross Sectional and Longitudinal Assessment of Neuropsychiatric Symptoms and Brain Functional Connectivity in Patients With Mild Cognitive Impairment, Cerebrovascular Disease and Parkinson Disease.

Authors: Rashidi‐Ranjbar, Neda Churchill, Nathan W. Black, Sandra E. et al.

Source: International Journal of Geriatric Psychiatry. Apr2025, Vol. 40 Issue 4, p1-14. 14p.

Subjects: Hippocampus physiology, Statistical models, Functional connectivity, Mild cognitive impairment, Research funding, Mental illness, Executive function, Central nervous system stimulants, Questionnaires, Default mode network, Parkinson's disease, Behavior, Appetite, Anxiety, Agitation (Psychology), Temporal lobe, Aggression (Psychology), Large-scale brain networks, Cerebrovascular disease, Cerebellum, Regression analysis, Apathy

A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort.

Authors: Moore, Katrina Convery, Rhian Bocchetta, Martina et al.

Source: Applied Neuropsychology: Adult. Jan/Feb 2022, Vol. 29 Issue 1, p112-119. 8p. 6 Charts, 1 Graph.

Bilingualism in Parkinson's disease: Relationship to cognition and quality of life.

Authors: Fishman, Keera N. Roberts, Angela C. Orange, J. B. et al.

Source: Journal of Clinical & Experimental Neuropsychology. Mar2021, Vol. 43 Issue 2, p199-212. 14p. 5 Charts.

Subjects: Bilingualism, Language ability, Parkinson's disease, Relationship quality, Dominant language, Executive function, Quality of life

The Return of Biomarker Results in Research: Balancing Complexity, Precision, and Ethical Responsibility.

Authors: Robillard, Julie M. Masellis, Mario Martin, Susanna E. et al.

Source: Journal of Alzheimer's Disease. 2024, Vol. 97 Issue 3, p1083-1090. 8p.

Association of sulfonylureas with the risk of dementia: A population‐based cohort study.

Authors: Wu, Che‐Yuan Iskander, Carina Wang, Christa et al.

Source: Journal of the American Geriatrics Society. Oct2023, Vol. 71 Issue 10, p3059-3070. 12p.

Subjects: Dementia risk factors, Public health surveillance, Alzheimer's disease, Confidence intervals, Insulin secretagogues, Retrospective studies, Hypoglycemic agents, Risk assessment, Type 2 diabetes, Comparative studies, Descriptive statistics, Research funding, Odds ratio, Longitudinal method, Enzyme inhibitors, Algorithms, Proportional hazards models, Disease complications

Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers.

Authors: Finger, Elizabeth Malik, Rubina Bocchetta, Martina et al.

Source: Brain: A Journal of Neurology; May2023, Vol. 146 Issue 5, p2120-2131, 12p

White matter hyperintensity burden predicts cognitive but not motor decline in Parkinson's disease: results from the Ontario Neurodegenerative Diseases Research Initiative.

Authors: Carvalho de Abreu, Daniela Cristina Pieruccini‐Faria, Frederico Sarquis‐Adamson, Yanina et al.

Source: European Journal of Neurology. Apr2023, Vol. 30 Issue 4, p920-933. 14p.

Subjects: Parkinson's disease, White matter (Nerve tissue), Neurodegeneration, Wechsler Adult Intelligence Scale, Gait disorders, Executive function

Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia.

Authors: Shafiei, Golia Bazinet, Vincent Dadar, Mahsa et al.

Source: Brain: A Journal of Neurology; Jan2023, Vol. 146 Issue 1, p321-336, 16p

Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.

Authors: Gasca-Salas, Carmen Masellis, Mario Khoo, Edwin et al.

Source: PLoS ONE. 4/21/2016, Vol. 11 Issue 4, p1-20. 20p.

MATERNAL SELF-REPORTED DEPRESSIVE SYMPTOMS AND MATERNAL CORTISOL LEVELS INTERACT TO PREDICT INFANT CORTISOL LEVELS.

Authors: Khoury, Jennifer E. Gonzalez, Andrea Levitan, Robert et al.

Source: Infant Mental Health Journal. Mar/Apr2016, Vol. 37 Issue 2, p125-139. 15p. 6 Charts, 4 Graphs.

Subjects: Depression in children, Hypothalamic-pituitary-adrenal axis, Hypothesis, Mother-infant relationship, Hydrocortisone

Reply: Is Pathology Always the Diagnostic Gold Standard in Neurodegeneration?

Authors: Ryan, Stephen A. Masellis, Mario Bilbao, Juan et al.

Source: Movement Disorders Clinical Practice. Nov2022, Vol. 9 Issue 8, p1154-1155. 2p.

Intra-Familial Clinical Heterogeneity due to FTLD-U with TDP-43 Proteinopathy Caused by a Novel Deletion in Progranulin Gene (PGRN).

Authors: Gabryelewicz, Tomasz Masellis, Mario Berdynski, Mariusz et al.

Source: Journal of Alzheimer's Disease. 2010, Vol. 22 Issue 4, p1123-1133. 11p. 4 Color Photographs, 1 Chart, 1 Graph.

Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders.

Authors: Ducharme, Simon Dols, Annemiek Laforce, Robert et al.

Source: Brain: A Journal of Neurology; Jun2020, Vol. 143 Issue 6, p1632-1650, 19p

A multiomics approach to heterogeneity in Alzheimer's disease: focused review and roadmap.

Authors: Badhwar, AmanPreet McFall, G Peggy Sapkota, Shraddha et al.

Source: Brain: A Journal of Neurology; May2020, Vol. 143 Issue 5, p1315-1331, 17p

Post COVID-19 condition is associated with altered regional cerebral blood volume as revealed by dynamic susceptibility contrast MRI.

Authors: MacIntosh, Bradley J. Lin, S. Shirley O'Hara, Finn et al.

Source: Frontiers in Neuroimaging. 2026, p1-10. 10p.

Cognitive profile of non-demented Parkinson's disease: Meta-analysis of domain and sex-specific deficits.

Authors: Curtis, Ashley F. Masellis, Mario Camicioli, Richard et al.

Source: Parkinsonism & Related Disorders. Mar2019, Vol. 60, p32-42. 11p.

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1 Sex Differences in Associations Between APOE ε2 and Longitudinal Cognitive Decline.

Authors: Wood, Madeline Xiong, Lisa Wong, Yuen Yan et al.

Source: Journal of the International Neuropsychological Society; 2023 Supplement, Vol. 29, p405-406, 2p

Dopamine receptor D2 (DRD2), dopamine transporter solute carrier family C6, member 4 (SLC6A3), and catechol-O-methyltransferase (COMT) genes as moderators of the relation between maternal history of maltreatment and infant emotion regulation

Authors: Villani, Vanessa Ludmer, Jaclyn Gonzalez, Andrea et al.

Source: Development & Psychopathology. May2018, Vol. 30 Issue 2, p581-592. 12p.

Subjects: Dopamine receptors, Self regulation, Genotypes, Behavioral assessment of children, Psychological distress