Because of the combined merits of rich physicochemical properties, abundance, low toxicity,
etc., hematite (α-Fe2O3), one of the most chemically stable compounds based on the …

Riboflavin transporter deficiency (RTD) is a rare genetic disorder characterized by motor,
sensory and cranial neuropathy. This childhood-onset neurodegenerative disease is caused …

Objective: Rare disease Background: Brown-Vialetto-Van Laere (BVVL) syndrome is a rare
autosomal recessive disorder caused by mutations in intestinal riboflavin transporter genes …

The neurotransmitter γ-hydroxybutyric acid (GHB) is suggested to be involved in neuronal
energy homeostasis processes, but the substance is also used as a recreational drug and …

Hereditary spastic paraplegia type 56 (SPG56-HSP) is a rare autosomal recessive disorder
caused by loss of function mutations in CYP2U1, leading to an early-onset limbs spasticity …