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Herrmann M, Obeid R, Scharhag J, Kindermann W, Herrmann W

Subjects were followed for 24 (VISP), 40 (NORVIT), 60 (HOPE-2), 88 (WAFACS), 41 (VITATOPS), or 80 months (SEARCH)

However, atrophic gastritis and pernicious anemia in patients with type 1 autoimmune polyglandular syndrome usually demonstrate low or normal gastrin levels, probably because of the loss of gastrin-producing cells (130)

Other systemic illnesses, such as diabetes and hyperthyroidism, or organ diseases affecting the liver and kidneys, can also contribute to deficiency by either preventing normal absorption or disrupting vitamin storage

[99] A person with cobalamin C disease, a rare autosomal, recessive, inheritance disease which results in combined methylmalonic aciduria and homocystinuria), [100] can be treated with intravenous or intramuscular hydroxocobalamin

Milk fat globular membranes (MFGM) contain four key compounds arranged in three layers: Glycerophospholipids, sphingolipids, cholesterol, and glycosphingolipids