Results 151 to 160 of about 33,332 (299)

Integrating a motor domain enhances disease severity scales in an FTD‐ALS spectrum cohort

open access: yesAlzheimer's &Dementia, Volume 21, Issue 10, October 2025.
Abstract INTRODUCTION The Genetic Frontotemporal Initiative (GENFI) and Advancing Research and Treatment in Frontotemporal Lobar Degeneration (ARTFL)‐Longitudinal Evaluation of Familial Frontotemporal Dementia Subjects (LEFFTDS) Longitudinal Frontotemporal Lobar Degeneration Study (ALLFTD) consortia developed Clinical Dementia Rating (CDR)‐derived ...
Allison Snyder   +17 more
wiley   +1 more source

Diplopia and eye movement disorders.

open access: yes, 2004
Published ...
Danchaivijitr, C, Kennard, C
core   +2 more sources

Beyond prion‐like spreading in neurodegenerative disease

open access: yesAlzheimer's &Dementia, Volume 21, Issue 10, October 2025.
Abstract To design effective therapies for neurodegenerative diseases, it is critical to understand the processes that trigger protein aggregation in sequential brain regions as the disease progresses. Aggregates formed in many neurodegenerative diseases, including Alzheimer's and Parkinson's disease, are capable of seeding, leading to the proposal to ...
Georg Meisl   +2 more
wiley   +1 more source

Frontal Tuberculoma Presenting With Atypical Foster Kennedy Syndrome in a Pregnant Patient

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Foster Kennedy syndrome (FKS), accounting for 1%–2.5% of intracranial masses, typically arises in the frontal lobe and may result from various etiologies, including rare causes such as tuberculoma. Although the incidence of central nervous system (CNS) tuberculosis is increasing, published reports in this setting remain scarce.
Kevin Aviles‐Largaespada   +4 more
wiley   +1 more source

Saccadic Eye Movement as a Harbinger of Gaucher's Disease in Children: A Case Report of Diagnostic Difficulty

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Gaucher disease type 3 (GD3) is a rare disorder causing neurological decline, including saccadic eye movement defects. A 2‐year‐old boy, initially treated for anemia, later developed gaze slowness, highlighting the need for careful assessment in children with eye movement issues.
Ramesh Khadayat   +8 more
wiley   +1 more source

O‐GlcNAcase Inhibitor Improves Denervation‐Induced Muscle Atrophy in Mice

open access: yesJournal of Cachexia, Sarcopenia and Muscle, Volume 16, Issue 5, October 2025.
ABSTRACT Background Skeletal muscle atrophy occurs in various situations, such as denervation, fasting and ageing. Disruption of the balance between protein synthesis and degradation plays an important role in muscle atrophy, and impaired Akt phosphorylation is considered to be crucial in this process.
Tomoyasu Suenaga   +8 more
wiley   +1 more source

Progressive supranuclear palsy

open access: yesČeská a slovenská neurologie a neurochirurgie, 2020
Tereza Bartošová, Jiří Klempíř
  +5 more sources

Effects of dance therapy on balance, gait and neuro-psychological performances in patients with Parkinson's disease and postural instability [PDF]

open access: yes, 2012
Postural Instability (PI) is a core feature of Parkinson’s Disease (PD) and a major cause of falls and disabilities. Impairment of executive functions has been called as an aggravating factor on motor performances. Dance therapy has been shown effective
Agnetti, Virgilio   +6 more
core  

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