Background and objectives: Wolfram syndrome (WFS) is a genetic disorder mainly caused by pathogenic variants in the WFS1 gene. It is characterized clinically by optic atrophy (OA), diabetes mellitus ...

Although the cerebellum is increasingly being viewed as a brain area involved in cognition, it typically is excluded from circuitry considered to mediate stimulant-associated behaviors since it is low ...

Figure 1: Western blot analysis of serum and CSF immunoreactivity to cdr2. Figure 2: Peripheral blood of PCD patients contains cdr2-specific killer cells. Figure 3: Enhanced CTL activity is detected ...

Biohaven shares tumbled in premarket trading Wednesday after the U.S. Food and Drug Administration turned away the clinical-stage biopharmaceutical company's proposed Vyglxia treatment for the rare ...

Investigator & Co-Director of the Neurotherapeutics IWI, Lundquist Institute (Formerly "LA BioMed"); Assistant Professor, David Geffen School of Medicine at UCLA Department of Neurology Ataxia ...

These findings provide evidence of the relevance of markers of cardiometabolic health for dementia among adults in China, ...

Heterozygous missense variants in the KIF21A gene are best known to cause congenital fibrosis of the extraocular muscles. A recent report by Borja et al., 2025 suggested that the KIF21A gene may also ...