What is the recommended protocol for switching from one glucagonlike peptide1 (GLP1) receptor agonist to another?
Huang YF, Wang PW, Huang LW, Lin MH, Yang W, Chen HC, Yu KP, Chen ML
Patients should inform at least one companion about their diabetes and how to recognize and respond to hypoglycemia
& Wasner, G
In 1993, it was discovered that Wilsons disease was caused by a mutation in the ATP7B gene, on chromosome 13, which resulted in absent or reduced function of a copperchaperone protein, ATP7B.14 ATP7B is a metal-transporting P-type ATPase, located on the trans-Golgi complex of the hepatocyte.15 The ATP7B protein is necessary for transport of copper into vesicles that form lysosomes for excretion into the bile
doi: 10.1081/JAS-120026089 260 MuleyPShahMMuleyA