Results 171 to 180 of about 2,880,433 (308)

Multimodal Autonomic Biomarkers Predict Phenoconversion in Pure Autonomic Failure

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Pure autonomic failure (PAF) presents with autonomic failure without other neurological features. A third develop central neurological features, fulfilling criteria for multiple system atrophy (MSA) and Lewy body diseases (LBD), including Parkinson's disease and Dementia with Lewy bodies.
S. Koay   +12 more
wiley   +1 more source

Distinct Regulation of Early Trafficking of the NMDA Receptors by the Ligand-Binding Domains of the GluN1 and GluN2A Subunits. [PDF]

open access: yesJ Neurosci
Netolicky J   +13 more
europepmc   +1 more source

GABAB receptor cell-surface export is controlled by an endoplasmic reticulum gatekeeper

open access: yesMolecular Psychiatry, 2016
Stéphane Doly   +16 more
semanticscholar   +1 more source

Comparative Effect of Standard Versus Extended Interval Dosing of Rituximab or Ocrelizumab in Multiple Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aimed to investigate the comparative effectiveness of standard versus personalized extended interval dosing of anti‐CD20 therapy on clinical and sub‐clinical outcomes in multiple sclerosis. Methods Clinical information was collected prospectively on Research Electronic Data Capture.
Nabil K. El Ayoubi   +6 more
wiley   +1 more source

ACLY promotes NK cell effector function by regulating glycolysis and histone acetylation. [PDF]

open access: yesJ Immunol
Sohn H   +10 more
europepmc   +1 more source

On-virus construction of polyvalent glycan ligands for cell-surface receptors.

open access: yesJournal of the American Chemical Society, 2008
Eiton Kaltgrad   +5 more
semanticscholar   +1 more source

Repeat Expansions in PLIN4 Cause Autosomal Dominant Vacuolar Myopathy With Sarcolemmal Features

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aim to describe and characterize two unrelated Spanish families suffering from an autosomal dominant autophagic vacuolar myopathy caused by repeat expansions in PLIN4. Methods We evaluated the clinical phenotype and muscle imaging, and performed a genetic workup that included exome sequencing, muscle RNAseq, and long‐read genome ...
Laura Llansó   +17 more
wiley   +1 more source

A Permeabilization Workflow To Enable Specific Multiplexed Profiling Using SERS Nanoparticles. [PDF]

open access: yesACS Appl Mater Interfaces
Bagheri P   +4 more
europepmc   +1 more source

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