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it is intended only as a diluent for medications that are subsequently administered per their approved routes and dosing
There is no official standard
Mutations in DDHD2, encoding an intracellular phospholipase A1, cause a recessive form of complex hereditary spastic paraplegia
According to the public registry, the trial was completed, and the results suggest a favorable safety profile with no significant adverse events reported (ClinicalTrials.gov Identifier: NCT03416053)
Research models cover traumatic brain injury, hippocampal ischemia, cuprizone-induced demyelination (a multiple sclerosis model), and spinal cord compression injury with tail paralysis
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