Results 161 to 170 of about 334,029 (292)

Functional MRI study of the visual system development in rodent model

open access: yes, 2009
The 4th World Congress on Bioengineering (WACBE 2009), Hong Kong, 26-29 July 2009.
Cheung, MMH, Xing, K, Chan, KCW, Wu, EX
core  

Quantitative MRI Uncovers Subtle Cortical Damage in Myelin Oligodendrocyte Glycoprotein Antibody‐Associated Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To determine whether myelin‐sensitive quantitative MRI reveals microstructural abnormalities in normal‐appearing cortex (NACtx) in myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD), indicating that conventional MRI underestimates remission residual cortical injury.
Valentina Camera   +20 more
wiley   +1 more source

Optimization of B-value in DTI- a Rat Brain Maturation Study

open access: yes, 2009
The 4th World Congress on Bioengineering (WACBE 2009), Hong Kong, 26-29 July 2009.
Cheung, MMH, Hui, ES, Wu, EX
core  

Natural Frequencies of Levodopa‐Induced Dyskinesia in Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives Abnormal involuntary movements, known as dyskinesias, are common complications of levodopa treatment in patients with Parkinson's disease and can significantly impair quality of life. The underlying pathophysiology remains unclear, and current therapeutic options are limited.
Ioannis U. Isaias   +3 more
wiley   +1 more source

Ultrahigh-field magnetic resonance imaging of normal and hypertensive eyes

open access: yes, 2009
The 4th World Congress on Bioengineering (WACBE 2009), Hong Kong, 26-29 July 2009.
Chan, KCW, So, KF, Fu, Q, Wu, EX
core  

Validation of a Cellular Imaging‐Based Method as a Potential Biomarker for SPG4 Hereditary Spastic Paraplegia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Hereditary Spastic Paraplegia (HSP) comprises a group of rare genetic diseases characterized by length‐dependent axonal degeneration of the corticospinal tracts and dorsal columns, whose main clinical feature is spastic gait. Pathogenic variants in the SPG4 gene cause Spastic Paraplegia Type 4 (SPG4‐HSP), the most common form of HSP.
Gaia Fattorini   +12 more
wiley   +1 more source

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