Results 221 to 230 of about 2,028,209 (354)
ABSTRACT Background X‐linked adrenoleukodystrophy (X‐ALD) is a neurometabolic disorder caused by pathogenic variants in ABCD1, leading to slowly progressive spinal cord disease in nearly all affected men. Sensitive biomarkers to quantify disease severity and predict progression are needed for clinical care and trial design.
Eda G. Kabak +4 more
wiley +1 more source
Rapid Assignment of Chemical Shifts From Crystal Structures in Solid-State NMR. [PDF]
Rodriguez-Madrid R, Holmes JB, Emsley L.
europepmc +1 more source
Predictive Ability of Plasma p‐tau217 for β‐Amyloid Status: A Prospective Multicenter Study
ABSTRACT Objective Plasma tau phosphorylated at threonine 217 (p‐tau217) measured with fully automated platforms has shown high accuracy for Alzheimer's disease (AD) diagnosis, but real‐world multicenter data remain limited. We aimed to validate the diagnostic performance of p‐tau217 for identifying AD pathology in a real‐world multicenter cohort ...
Miquel Massons +33 more
wiley +1 more source
An experimental perspective on symmetry breaking and the singlet fission mechanism in solid-state materials. [PDF]
Xu X, Hall CR, Smith TA.
europepmc +1 more source
Safety and Tolerability of Givinostat: Evidence From Real‐World and Clinical Practice
ABSTRACT Objective The aim of our study was to establish the prevalence of adverse events in a real‐world setting in boys living with Duchenne muscular dystrophy (DMD) treated with givinostat as part of an Expanded Access Program (EAP) in Italy. Methods The cohort included 90 ambulant boys, with age when treatment started between 6 and 23 years (mean ...
Marika Pane +19 more
wiley +1 more source
Synthesis of TiB2-TiC Composites by the Solid-State Reaction between B4C and Ti Powders.
Hitoshi Taimatsu +3 more
openalex +2 more sources
2D Metal-Organic Frameworks for High-Performance Solid-State Electrolytes: A Comprehensive Review. [PDF]
Ai C +8 more
europepmc +1 more source
Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach +23 more
wiley +1 more source
A Scalable Method for Cavity-Enhanced Solid-State Quantum Sensors. [PDF]
Tibben DJ +5 more
europepmc +1 more source

