Results 201 to 210 of about 1,684,670 (310)

CSF Levels of NPTX2 Are Associated With Less Brain Atrophy Over Time in Cognitively Unimpaired Individuals

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Neuronal pentraxin 2 (NPTX2) is a synaptic protein involved in synaptic plasticity and regulation of neuronal excitability. Lower baseline cerebrospinal fluid (CSF) NPTX2 levels have been shown to be associated with an earlier onset of mild cognitive impairment (MCI), a pre‐dementia syndrome, even after CSF Alzheimer's Disease (AD)
Juan P. Vazquez   +12 more
wiley   +1 more source

Planetary sources of bio-essential nutrients on a prebiotic world. [PDF]

open access: yesPhilos Trans R Soc Lond B Biol Sci
Galloway T   +3 more
europepmc   +1 more source

‘Let's see if you can see me': making connections with Google Earth™ in a preschool classroom [PDF]

open access: green, 2016
Susan Danby   +4 more
openalex   +1 more source

Tipping elements in the Earth's climate system

open access: yesProceedings of the National Academy of Sciences of the United States of America, 2008
T. Lenton   +6 more
semanticscholar   +1 more source

Diffusion Tractography Biomarker for Epilepsy Severity in Children With Drug‐Resistant Epilepsy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To develop a novel deep‐learning model of clinical DWI tractography that can accurately predict the general assessment of epilepsy severity (GASE) in pediatric drug‐resistant epilepsy (DRE) and test if it can screen diverse neurocognitive impairments identified through neuropsychological assessments.
Jeong‐Won Jeong   +7 more
wiley   +1 more source

Relativistic perihelion precession of orbits of Venus and the Earth

open access: yesOpen Physics, 2008
Biswas Abhijit, Mani Krishnan
doaj   +1 more source

Trophic Downgrading of Planet Earth

open access: yesScience, 2011
J. Estes   +23 more
semanticscholar   +1 more source

Nationwide Characterization of MFN2‐Related CMT in 176 Japanese Patients: Clinical and Genetic Insights

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando   +13 more
wiley   +1 more source

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