Results 261 to 270 of about 4,562,205 (344)
Functional Neuroimaging to Characterize Visual System Development in Children with Retinoblastoma
Scott Barb+11 more
openalex +1 more source
Functional neuroimaging of narcolepsy
Dang-Vu, Thanh, Schwartz, Sophie
openaire +2 more sources
Blepharospasm in GNAO1 Syndrome May Benefit From Botulinum Toxins
Movement Disorders Clinical Practice, EarlyView.
Eleonora Minacapilli+4 more
wiley +1 more source
ABSTRACT Background Parkinson's disease (PD) varies widely across individuals in clinical manifestations and course of progression. Identification of distinct biological subtypes could explain this heterogeneity, identify its pathophysiology, and predict disease progression. Objectives Our aim was to compare longitudinal clinical trajectories and brain
Seyed‐Mohammad Fereshtehnejad+7 more
wiley +1 more source
ABSTRACT Neuroimaging with positron emission tomography (PET) has been instrumental in elucidating neurobiological mechanisms behind therapeutical trials in Parkinson's disease (PD). A variety of medical and neurosurgical interventions have been evaluated using many radioligands that reveal molecular basis for target engagement and brain responses in ...
Vijay Dhawan+4 more
wiley +1 more source
Neural Mechanisms of Object Location Memory in Huntington's Disease
ABSTRACT Background Object‐location memory impairment in Huntington's disease (HD) occurs from premanifest period and declines as HD progresses, however, pathogenesis of object‐location memory is unknown. The striatum and hippocampus are affected in HD, functionally interacting allowing intact object‐location memory.
Yifat Glikmann‐Johnston+4 more
wiley +1 more source
Fractionating difficulty during sentence comprehension using functional neuroimaging. [PDF]
Thothathiri M+3 more
europepmc +1 more source
Functional and effective connectivity in neuroimaging: A synthesis
Karl J. Friston
semanticscholar +1 more source
Identification of GGC Repeat Expansions in ZFHX3 among Chilean Movement Disorder Patients
Abstract Background Hereditary ataxias are genetically diverse, yet up to 75% remain undiagnosed due to technological and financial barriers. The GGC repeat expansion in ZFHX3, responsible for spinocerebellar ataxia type 4 (SCA4), has only been described in individuals of Northern Europeandescent.
Paula Saffie‐Awad+22 more
wiley +1 more source