Results 131 to 140 of about 2,341,112 (317)

Structure–Function Decoupling of the Sensorimotor and Default Mode Networks in Black Americans With MS

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Multiple sclerosis (MS) exhibits racially disparate rates of disease progression. Black people with MS (B‐PwMS) experience a more severe disease course than non‐Hispanic White people with MS (NHW‐PwMS). Here we investigated structural and functional connectivity as well as structure–function decoupling in the ...
Emilio Cipriano   +11 more
wiley   +1 more source

The Ohio State University Libraries Faculty Meeting Minutes, December 11, 2007

open access: yes, 2007
The University Archives has determined that this item is of continuing value to OSU's ...
Ohio State University. Libraries
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Complementarity of Long‐Reads and Optical Mapping in Parkinson's Disease for Structural Variants

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Long‐read sequencing and optical genome mapping technologies have the ability to detect large and complex structural variants. This has led to the discovery of novel pathogenic variants in neurodegenerative movement disorders. Thus, we aimed to systematically compare the SV detection capabilities of OGM and ONT in Parkinson's disease.
André Fienemann   +17 more
wiley   +1 more source

The Ohio State University Libraries Faculty Meeting Minutes, October 1, 2024

open access: yes
The University Archives has determined that this item is of continuing value to OSU's ...
Ohio State University. Libraries
core  

The Ohio State University Libraries Faculty Meeting Minutes, February 5, 2013

open access: yes, 2012
The University Archives has determined that this item is of continuing value to OSU's ...
Ohio State University. Libraries
core  

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina   +11 more
wiley   +1 more source

The Ohio State University Libraries Faculty Meeting Minutes, April 14, 2020

open access: yes, 2020
The University Archives has determined that this item is of continuing value to OSU's ...
Ohio State University. Libraries
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FDG‐PET Associations With Disease Severity and Outcomes in NMDA‐Receptor IgG Autoimmune Encephalitis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Patients with N‐methyl‐D‐aspartate (NMDA) receptor‐immunoglobulin G (IgG) autoimmune encephalitis (NMDAR‐IgG AE) demonstrate occipital lobe hypometabolism on baseline brain fluorodeoxyglucose‐positron emission tomography (bFDG‐PET).
Jonathan K. Lee   +7 more
wiley   +1 more source

The Ohio State University Libraries Faculty Meeting Agenda, March 19, 2019

open access: yes, 2019
The University Archives has determined that this item is of continuing value to OSU's ...
Ohio State University. Libraries
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