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These include 1) congenital pernicious anaemia, where there is a genetic defect in IF synthesis, leading to B12 malabsorption, 2) Imerslund-Grsbeck Syndrome (IGS) caused by mutations in genes encoding cubulin and amnionless , 3) inherited HC or TCII deficiencies, and 4) intracellular cobalamin defects (CblA-CblG defects)

doi: 10.1093/plphys/kiab600 22 LiN.ShangJ

Revival of Damaged Skin - The polynucleotides in Lumi Eyes repair damage to the dermis, fostering the regeneration of cells and tissues

While there have been no clinical randomized controlled studies to validate the clinical efficacy of ustekinumab in treating AA, the promising results seen in these case reports warrant further exploration of its potential in the future

Intestinal dysbiosis and hormonal neuroendocrine secretion in the fibromyalgic patient