Results 211 to 220 of about 8,570,567 (357)

Generalized thermalization in quenched free Fermionic models

open access: yes, 2018
We investigate generalized thermalization in an isolated free Fermionic chain evolving from an out of equilibrium initial state through a sudden quench. We consider the quench where a Fermionic chain is broken into two disjoint chains.
Byju, Sandra   +2 more
core  

Ontogenesis of myosin light chain phosphorylation in guinea pig tracheal smooth muscle

open access: green, 2004
Pasquale Chitano   +11 more
openalex   +1 more source

The Diverse Neuromuscular Spectrum of VPS13A Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective VPS13A disease (chorea‐acanthocytosis) is a rare neurodegenerative disorder caused by biallelic variants in VPS13A, typically presenting with hyperkinetic movement disorders, while neuromuscular signs are often mild. The aim of the project was to investigate the frequency and severity of neuromuscular impairment in VPS13A disease ...
Anne Buchberger   +16 more
wiley   +1 more source

Annual 12‐Week Dosing Gap of Natalizumab: Clinical Efficacy, Blood Biomarkers, and CSF Cell Composition

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Natalizumab (NTZ) is a highly effective therapy for multiple sclerosis (MS); however, its use is limited by the risk of a rare potentially severe opportunistic brain infection, progressive multifocal leukoencephalopathy (PML). Alternative dosing strategies are evaluated to reduce PML risk while still maintaining efficacy, which ...
Regina Berkovich   +10 more
wiley   +1 more source

Timely Intervention in Light Chain Cardiac Amyloidosis. [PDF]

open access: yesJACC Case Rep
Rahman A   +3 more
europepmc   +1 more source

Serum neurofilament light chain withstands delayed freezing and repeated thawing [PDF]

open access: gold, 2020
Patrick Altmann   +21 more
openalex   +1 more source

Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam   +6 more
wiley   +1 more source

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