Results 211 to 220 of about 514,621 (311)

A Depolarizing Leak in Sodium Bicarbonate Cotransporter NBCe1 Causes Brain Edema

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives SLC4A4 encodes electrogenic sodium bicarbonate cotransporter NBCe1, prominently expressed in kidney and brain. Recessive loss‐of‐function variants in SLC4A4 cause proximal renal tubular acidosis, no brain edema. In the brain, NBCe1 is expressed by astrocytes, where it regulates pH and mediates astrocyte volume changes.
Quinty Bisseling   +16 more
wiley   +1 more source

CSF Monoamine Metabolites and Cognitive Trajectory in Early Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Imaging and postmortem studies indicate that abnormalities in monoaminergic neurotransmission contribute to cognitive impairment in Parkinson's disease (PD). However, it remains uncertain if cerebrospinal fluid (CSF) monoamine metabolites can serve as biomarkers of cognitive decline in early PD.
Jing‐Yu Shao   +7 more
wiley   +1 more source

The 11-Item Weight-Related Behaviours Questionnaire-Short Form (WRB-Q-SF): New Psychometric Evidence for the Arabic Version in Pregnant Women

open access: yesInternational Journal of Women's Health
Nour Al Hage,1 Sahar Obeid,2 Fouad Sakr,3 Mariam Dabbous,3 Patrick Zaarour,1,4 Souheil Hallit,1,5 Feten Fekih-Romdhane6,7 1School of Medicine and Medical Sciences, Holy Spirit University of Kaslik, Jounieh, Lebanon; 2Social and Education Sciences ...
Al Hage N   +6 more
doaj  

GL261 glioblastoma induces delayed body weight gain and stunted skeletal muscle growth in young mice. [PDF]

open access: yesAm J Physiol Regul Integr Comp Physiol
Huot JR   +6 more
europepmc   +1 more source

Effect of a light-darkness cycle on the body weight gain of preterm infants admitted to the neonatal intensive care unit. [PDF]

open access: yesSci Rep, 2022
Sánchez-Sánchez M   +19 more
europepmc   +1 more source

SPG4 and Dementia: Expanding the Clinical Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza   +19 more
wiley   +1 more source

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