DRUG EFFECT;
DRUG MECHANISM;
HYPOGLYCEMIA;
NON INSULIN DEPENDENT DIABETES MELLITUS;
SHORT SURVEY;
ARTICLE;
COMPARATIVE STUDY;
DIABETES MELLITUS;
HUMAN;
ORAL DRUG ADMINISTRATION;
SECRETION;
Comparison between repaglinide and glipizide in Type 2 diabetes mellitus: A 1-year multicentre study
Madsbad S, Kilhovd B, Lager I, Mustajoki P, Dejgaard A. Comparison between repaglinide and glipizide in Type 2 diabetes mellitus: a 1-year multicentre study. Diabetic Med 2001; 18: 395-401.
Rapid and short acting mealtime insulin secretion with nateglinide controls both prandial and mean glycemia
Hanefeld M, Bouter KP, Dickinson S, Guitard C. Rapid and short acting mealtime insulin secretion with nateglinide controls both prandial and mean glycemia. Diabetes Care 2000; 23: 202-7.
Lower incidence of severe hypoglycaemia in patients with type 2 diabetes treated with glimepiride versus glibenclamide
Holstein A, Plaschke A, Egberts E. Lower incidence of severe hypoglycaemia in patients with type 2 diabetes treated with glimepiride versus glibenclamide. Diabetes Metab Res Rev 2001; 17: 467-73.
Glimepiride, a novel sulfonylurea, does not abolish myocardial protection afforded by either ischemic preconditioning or diazoxide
Mocanu MM, Maddock HL, Baxter GF, Lawrence CL, Standen NB, Yellon DM. Glimepiride, a novel sulfonylurea, does not abolish myocardial protection afforded by either ischemic preconditioning or diazoxide. Circulation 2001; 103: 3111-6.
Intensive blood-glucose control with sulphonylurea or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)
UK Prospective Diabetes Study (UKPDS) Group. Intensive blood-glucose control with sulphonylurea or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet 1998; 352: 837-53.