Glucose transporter-1 deficiency syndrome is caused by mutations in the SLC2A1 gene in
the majority of patients and results in impaired glucose transport into the brain. From 2004–…

In the mouse, neurotransmitter metabolism can be regulated by modulation of the synthesis
of pyridoxal 5′-phosphate and failure to maintain pyridoxal phosphate (PLP) levels results …

Purpose Infantile Pompe disease resulting from a deficiency of lysosomal acid α-glucosidase
(GAA) requires enzyme replacement therapy (ERT) with recombinant human GAA (rhGAA). …

Recent research has demonstrated broad benefits of video game play to perceptual and
cognitive abilities. These broad improvements suggest that video game-based cognitive …

Objective: Charcot-Marie-Tooth (CMT) disease is the most common inherited neuromuscular
disorder, affecting 1 in 2,500 individuals. Mitochondrial DNA (mtDNA) mutations are not …

BACKGROUND Medium chain acyl-CoA dehydrogenase (MCAD) deficiency is the most
common inborn error of fatty acid metabolism. Undiagnosed, it has a mortality rate of 20–25%. …

Situation awareness (SA) in the cyber security domain is particularly relevant to teams of
security analysts who are responsible for detecting cyber threats by perusing continual floods of …

Transport And Golgi Organization protein 2 (TANGO2) deficiency has recently been identified
as a rare metabolic disorder with a distinct clinical and biochemical phenotype of recurrent …

LonP1 is a mitochondrial matrix protease whose selective substrate specificity is essential
for maintaining mitochondrial homeostasis. Recessively inherited, pathogenic defects in …

… Champion, Michael W. Explaining the cosmos: creation and cultural interaction in late-antique
Gaza / Michael W. Champion. pages cm.—(Oxford studies in late antiquity) Includes …