Results 111 to 120 of about 1,335,420 (346)

Diffusion Basis Spectrum Imaging of Tissue Microstructure and Early Treatment in Multiple Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Conventional MRI cannot resolve the coexisting pathological processes within multiple sclerosis tissue. Diffusion Basis Spectrum Imaging decomposes the diffusion signal into fiber, cell, and hindered ratios indexing axonal integrity, cellularity, and extracellular space, respectively.
Apisit Kaewsanit   +10 more
wiley   +1 more source

Axial Function Reflects Global Severity in Inherited Ataxias: The Upright Stability Score in Ambulatory Friedreich vs. Spinocerebellar Ataxia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Inherited ataxias are clinically diverse neurodegenerative diseases, complicating the choice of outcome measures for trials. In spinocerebellar ataxia (SCA), regulatory concerns about the Scale for the Assessment and Rating of Ataxia (SARA) caused a shift toward functional SARA (f‐SARA), contributing to pivotal trial failure.
Christian Rummey   +52 more
wiley   +1 more source

Left Ventricular Hypertrabeculation (LVHT) in Athletes: A Negligible Finding?

open access: yesMedicina
Left ventricular hypertrabeculation (LVHT) used to be a rare phenotypic trait. With advances in diagnostic imaging techniques, LVHT is being recognised in an increasing number of people.
Rokas Jagminas   +3 more
doaj   +1 more source

Sensitivity analysis showing the omission of rare species has negligible effects.

open access: yes, 2023
Small followup sensitivity analysis showing that the omission of rare species has a negligible effect on the results we present in the main text. 
William Godsoe (11956847)   +1 more
core   +1 more source

Parkinson Disease Subtype Stability and Eventual Convergence

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Previous research identified distinct Parkinson disease (PD) clinical subtypes of “Motor Only,” “Psychiatric & Motor,” and “Cognitive & Motor” based on comprehensive, multidomain classification. Whether these subtypes reflect distinct trajectories or progressive disease stages remains unknown.
Laura M. Rosok   +10 more
wiley   +1 more source

NEGLIGIBLE CREEP OF P91 STEEL

open access: yes, 2014
To avoid inclusion of the possible creep effects during normal service operation in future nuclear plants in the component design, it is important to define temperature, stress and time limits for negligible creep for P91 steel.
LUZGINOVA Natalia, HOLMSTROM Bjorn
core   +1 more source

Negligible-cost microfluidic device fabrication using 3D-printed interconnecting channel scaffolds

open access: yes, 2020
Data supporting the journal paper - Negligible-cost microfluidic device fabrication using 3D-printed interconnecting channel scaffolds - published in PLOS ...
Gaxiola, Andrea Diaz   +2 more
core   +1 more source

Serostatus‐Specific Prognostic Profiles and Phenotype‐Dependent Therapeutic Windows in Autoimmune Encephalitis: A Multicenter Cohort Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background While autoimmune encephalitis (AE) outcomes vary, serostatus‐specific prognostic determinants and institutional clustering effects remain poorly characterized. We aimed to delineate the distinct prognostic architecture of AE, identifying serostatus‐specific risk factors and potential therapeutic windows.
Xiaohong Tang   +17 more
wiley   +1 more source

Negligible release of cardiolipin during milk secretion by the ruminant

open access: yesJournal of Lipid Research, 1969
The presence of cardiolipin (diphosphatidyl glycerol) in lactating mammary tissue (cow and goat) was investigated. The tissue was separated into subcellular fractions by sedimentation; the identities of the fractions were confirmed by electron microscopy.
Stuart Patton, L.F. Hood, J.S. Patton
doaj   +1 more source

Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

open access: yesNature Genetics, 2015
We propose a method (GREML-LDMS) to estimate heritability for human complex traits in unrelated individuals using whole-genome sequencing data. We demonstrate using simulations based on whole-genome sequencing data that ∼97% and ∼68% of variation at ...
Jian Yang   +23 more
semanticscholar   +1 more source

Home - About - Disclaimer - Privacy