The set of journals have been ranked according to their SJR and divided into four equal groups, four quartiles. Q1 (green) comprises the quarter of the journals with the highest values, Q2 (yellow) the second highest values, Q3 (orange) the third highest values and Q4 (red) the lowest ...
Action impulsivity and attention deficits in patients at an early stage of Huntington disease Sacha Brohée Stephan Grimaldi Marianne Vaugoyeau Neurology and Preclinical Neurological Studies - Original Article 03 March 2025 Comparison of inflammatory biomarker levels in neurodegenerative proteinopathies:...
CD-163, and HLA-DR positive cells (indicating infiltrating monocytes or resident microglia activation), elevated pro-inflammatory markers (Interleukin-1β, IL1-β; cycloxygenase 2, COX2), increased Aβ42 deposition (the hallmark disease protein of Alzheimer's disease), blood...
Behavioral Neuroscience contributes strongly to the understanding of medical disorders and has contributed important therapeutic data on variety of conditions, including: Parkinson's Disease, Alzheimer's Disease, Huntington's Disease, Clinical Depression, Schizophrenia, Autism, Anxiety, etc. Cognitive ...
Disintegration of the sleep-wake cycle and circadian timing in Huntington's disease. Sleep disturbances in neurological disorders have a devastating impact on patient and carer alike. However, their pathological origin is unknown. Here we s... Morton,J A. - 《Journal of Neuroscience》 被引量: ...
Huntington’s disease (HD) is one of neurodegenerative diseases, and is defined as a monogenetic disease due to the mutation of Huntingtin gene. This disease affects several cellular functions in neurons, and further influences motor and cognitive abilit
Huntington's disease (HD) is caused by an increase in the number of CAG repeats in the huntingtin gene (HTT). The greater the number of repeats, the earlier the onset and more severe the symptoms tend to be. In particular, neurons in the striatum of the brain are the most susceptible ...
期刊名称:《The Journal of Neuroscience》 | 2011年第26期 11.Peroxisome-Proliferator-Activated Receptor Gamma Coactivator 1 α Contributes to Dysmyelination in Experimental Models of Huntingtons Disease 机译:过氧化物酶体增殖物激活的受体γ共激活因子1α促成亨廷顿氏病实验模型中的脱髓鞘 作者:Zhongmin Xian...
select article A global role for the world federation of neurology Conference abstractFull text access A global role for the world federation of neurology W.M. Carroll Pages 2-3 View PDF select article Treating Huntington’s disease Conference abstractFull text access ...
Huntington's disease (HD) is an inherited neurodegenerative disorder characterized by cortico-striatal dysfunction and loss of glutamate uptake. At 7 weeks of age, R6/2 mice, which model an aggressive form of juvenile HD, show a glutamate-uptake deficit