-
1
-
-
15044354104
-
GIP and GLP-1, as inrecitin hormones, lessons from single and double inrecitin receptor knockout mice
-
Hansotia, T., Drucker, D. J.: GIP and GLP-1, as inrecitin hormones, lessons from single and double inrecitin receptor knockout mice. Regul. Pept. 2005, 128, 125-134.
-
(2005)
Regul. Pept
, vol.128
, pp. 125-134
-
-
Hansotia, T.1
Drucker, D.J.2
-
2
-
-
2642519637
-
Treatment of type 2 diabetes mellitus with agonists of the GLP-1 receptor or DPP-inhibitors
-
Holst, J. J.: Treatment of type 2 diabetes mellitus with agonists of the GLP-1 receptor or DPP-inhibitors. Exp. Opin. Emerg. Drugs, 2004, 9, 155-166.
-
(2004)
Exp. Opin. Emerg. Drugs
, vol.9
, pp. 155-166
-
-
Holst, J.J.1
-
3
-
-
34848840532
-
A glukagonszerü peptid (GLP)-1 részvétele a szénhidrát-anyagcsere szábályozásában, receptor agonistái és analógjai potenciális helye a 2-es típusú diabetes mellims jövobeni terápiájában
-
Winkler G., Cseh K.: A glukagonszerü peptid (GLP)-1 részvétele a szénhidrát-anyagcsere szábályozásában, receptor agonistái és analógjai potenciális helye a 2-es típusú diabetes mellims jövobeni terápiájában. Diabetol. Hung., 2002, 12, 187-197.
-
(2002)
Diabetol. Hung
, vol.12
, pp. 187-197
-
-
Winkler, G.1
Cseh, K.2
-
4
-
-
34848882417
-
Az inkretinmimetikum exenatid - új kezelési lehetoség a 2-es típusú diabetesben
-
Winkler G., Cseh K.: Az inkretinmimetikum exenatid - új kezelési lehetoség a 2-es típusú diabetesben. Diabetol. Hung., 2005, 13 (Suppl. 3), 20-29.
-
(2005)
Diabetol. Hung
, vol.13
, Issue.SUPPL. 3
, pp. 20-29
-
-
Winkler, G.1
Cseh, K.2
-
5
-
-
0942279564
-
-
Gastaldelli, A., Ferrannini, E., Miyazaki, Y. és mtsai: Betacell dysfunction and glucose intolerance: results from the San Antonio Metabolism (SAM) Study. Diabetologia, 2004, 47, 31-39.
-
Gastaldelli, A., Ferrannini, E., Miyazaki, Y. és mtsai: Betacell dysfunction and glucose intolerance: results from the San Antonio Metabolism (SAM) Study. Diabetologia, 2004, 47, 31-39.
-
-
-
-
6
-
-
0037382455
-
Contributions of insulin-resistance, an insulinsecretory defects to the pathogenesis of type 2 diabetes mellitus
-
Gerich, J. E.: Contributions of insulin-resistance, an insulinsecretory defects to the pathogenesis of type 2 diabetes mellitus. Mayo Clin. Proc., 2003, 78, 447-456.
-
(2003)
Mayo Clin. Proc
, vol.7
, Issue.8
, pp. 447-456
-
-
Gerich, J.E.1
-
7
-
-
34047096301
-
Glucose inhibits glucagon secretion by a direct effect on mouse pancreatic alpha cells
-
Vieira, E., Salehi, A., Gylfe, E.: Glucose inhibits glucagon secretion by a direct effect on mouse pancreatic alpha cells. Diabetologia, 2007, 50, 370-379.
-
(2007)
Diabetologia
, vol.50
, pp. 370-379
-
-
Vieira, E.1
Salehi, A.2
Gylfe, E.3
-
8
-
-
24944577486
-
-
Dunning, B. E., Foley, J. E., Ahrén, B.: Alpha cell function in health and disease: influence of glucagon-like peptide-1. Diabetologia, 2005, 48, 1700-1713.
-
Dunning, B. E., Foley, J. E., Ahrén, B.: Alpha cell function in health and disease: influence of glucagon-like peptide-1. Diabetologia, 2005, 48, 1700-1713.
-
-
-
-
9
-
-
33745301045
-
-
Meier, J. J., Kjems, L. L., Veldhuis, J. D. és mtsai: Postprandial suppression of glucagon secretion depends on intact pulsatile insulin secretion. Further evidence for the intraislet hypothesis. Diabetes, 2006, 55, 1051-1056.
-
Meier, J. J., Kjems, L. L., Veldhuis, J. D. és mtsai: Postprandial suppression of glucagon secretion depends on intact pulsatile insulin secretion. Further evidence for the intraislet hypothesis. Diabetes, 2006, 55, 1051-1056.
-
-
-
-
10
-
-
66749175733
-
Alpha-cell function in type 2 diabetes
-
Lefébvre, P.: Alpha-cell function in type 2 diabetes. European Endocrine Disease, 2006. pp. 3-4 (www.touchbriefings. com).
-
(2006)
European Endocrine Disease
, pp. 3-4
-
-
Lefébvre, P.1
-
11
-
-
12244284000
-
Beta- and alpha cell dysfunction in type 2 diabetes
-
Del Prato, S., Marchetti, P.: Beta- and alpha cell dysfunction in type 2 diabetes. Horm. Metab. Res., 2004, 36, 775-781.
-
(2004)
Horm. Metab. Res
, vol.36
, pp. 775-781
-
-
Del Prato, S.1
Marchetti, P.2
-
12
-
-
27744560292
-
Deconvolution analysis of rapid insulin pulses before and after six weeks of continuous subcutaneous administration of glucagon-like peptide-1 in elderly patients with Type 2 diabetes
-
Meneilly, G. S, Veldhuis, J. D., Elahi, D.: Deconvolution analysis of rapid insulin pulses before and after six weeks of continuous subcutaneous administration of glucagon-like peptide-1 in elderly patients with Type 2 diabetes. J. Clin. Endocr. Metab., 2005, 90, 6251-6256.
-
(2005)
J. Clin. Endocr. Metab
, vol.90
, pp. 6251-6256
-
-
Meneilly, G.S.1
Veldhuis, J.D.2
Elahi, D.3
-
13
-
-
33644618433
-
-
Drucker, D, J.: The biology of incretine hormones. Cell. Metab., 2006, 3, 153-165.
-
Drucker, D, J.: The biology of incretine hormones. Cell. Metab., 2006, 3, 153-165.
-
-
-
-
14
-
-
21744433419
-
-
Gautier, J. F., Fetita, S., Sobngwi, E. és mtsai: Biological actions of the incretins GIP and GLP-1 and therapeutic perspectives in patients with type 2 diabetes. Diabetes Metab., 2005, 31, 233-242.
-
Gautier, J. F., Fetita, S., Sobngwi, E. és mtsai: Biological actions of the incretins GIP and GLP-1 and therapeutic perspectives in patients with type 2 diabetes. Diabetes Metab., 2005, 31, 233-242.
-
-
-
-
15
-
-
31844443202
-
Glucagon-like peptide-l: From extract to agent. The Claude Bernard Lecture
-
Holst, J.: Glucagon-like peptide-l: from extract to agent. The Claude Bernard Lecture. Diabetologia, 2006, 49, 253-260.
-
(2006)
Diabetologia
, vol.49
, pp. 253-260
-
-
Holst, J.1
-
16
-
-
0038121744
-
-
Vilsbøll, T., Krarup, T., Madsbad, S. és mtsai: Both GLP-1 and GIP are insulinotropic at basal at postprandial glucose levels and contribute nearly equally to the incretin effect of a meal in healthy subjects. Regul. Pept., 2003, 114, 115-121.
-
Vilsbøll, T., Krarup, T., Madsbad, S. és mtsai: Both GLP-1 and GIP are insulinotropic at basal at postprandial glucose levels and contribute nearly equally to the incretin effect of a meal in healthy subjects. Regul. Pept., 2003, 114, 115-121.
-
-
-
-
17
-
-
21344451403
-
-
Mannucci, E., Pala, L., Ciani, S. és mtsai: Hyperglycaemia increases dipeptidyl peptidase IV activity in diabetes mellitus. Diabetologia, 2005, 48, 1168-1172.
-
Mannucci, E., Pala, L., Ciani, S. és mtsai: Hyperglycaemia increases dipeptidyl peptidase IV activity in diabetes mellitus. Diabetologia, 2005, 48, 1168-1172.
-
-
-
-
18
-
-
33846006173
-
The incretin system: Glucagonlike peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes
-
Drucker, D. J, Nauck, M. A.: The incretin system: glucagonlike peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes. Lancet, 2006, 368, 1696-1705.
-
(2006)
Lancet
, vol.368
, pp. 1696-1705
-
-
Drucker, D.J.1
Nauck, M.A.2
-
19
-
-
3843072211
-
Dipeptidyl peptidase IV inhibitors for the treatment of diabetes
-
Weber, A. E.: Dipeptidyl peptidase IV inhibitors for the treatment of diabetes. J. Med. Chem., 2004, 47, 4135-4141.
-
(2004)
J. Med. Chem
, vol.47
, pp. 4135-4141
-
-
Weber, A.E.1
-
20
-
-
33845476757
-
J. és mtsai (for the Sitagliptin Study 020 Group): Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagpliptin added to ongoing metformin therapy in patients with type 2 diabetes inadequately controlled with metformin alone
-
Charbonnel, B., Karasik, A., Liu, J. és mtsai (for the Sitagliptin Study 020 Group): Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagpliptin added to ongoing metformin therapy in patients with type 2 diabetes inadequately controlled with metformin alone. Diabetes Care, 2006, 29, 2638-2643.
-
(2006)
Diabetes Care
, vol.29
, pp. 2638-2643
-
-
Charbonnel, B.1
Karasik, A.2
Liu3
-
21
-
-
14044264798
-
Glucagon-like peptide-1 and inhibitors of dipeptidyl peptidase IV in the treatment of type 2 diabetes mellitus
-
Holst, J. J., Deacon, C. F.: Glucagon-like peptide-1 and inhibitors of dipeptidyl peptidase IV in the treatment of type 2 diabetes mellitus. Curr. Opin. Pharmacol., 2004, 4, 589-596.
-
(2004)
Curr. Opin. Pharmacol
, vol.4
, pp. 589-596
-
-
Holst, J.J.1
Deacon, C.F.2
-
22
-
-
0037342614
-
-
Pospisilik, J. A., Martin, J., Doty, T. és mtsai: Dipeptidyl peptidase IV inhibitor treatment stimulates β-cell survival and islet neogenesis in streptozotocin-induced diabetic rats. Diabetes, 2003, 52, 741-750.
-
Pospisilik, J. A., Martin, J., Doty, T. és mtsai: Dipeptidyl peptidase IV inhibitor treatment stimulates β-cell survival and islet neogenesis in streptozotocin-induced diabetic rats. Diabetes, 2003, 52, 741-750.
-
-
-
-
23
-
-
33748331194
-
Y-P. és mtsai: Chronic inhibition of dipeptidyl peptidase-4 with a sitagliptin analog preserves pancreatic β-cell mass and function in a rodent model of type 2 diabetes
-
Mu, J., Woods, J., Zhou, Y-P. és mtsai: Chronic inhibition of dipeptidyl peptidase-4 with a sitagliptin analog preserves pancreatic β-cell mass and function in a rodent model of type 2 diabetes. Diabetes, 2006, 55, 1695-704.
-
(2006)
Diabetes
, vol.55
, pp. 1695-1704
-
-
Mu, J.1
Woods, J.2
Zhou3
-
24
-
-
33646492251
-
-
Xu, L., Kaneto, H., Lopez-Avalos, M. D. és mtsai: GLP1/ exendin-4 facilitates β-cell neogenesis in rat and human pancreatic ducts. Diab. Res. Clin. Pract., 2006, 3, 107-110.
-
Xu, L., Kaneto, H., Lopez-Avalos, M. D. és mtsai: GLP1/ exendin-4 facilitates β-cell neogenesis in rat and human pancreatic ducts. Diab. Res. Clin. Pract., 2006, 3, 107-110.
-
-
-
-
25
-
-
4544232468
-
Inhibition of dipeptidyl peptidase IV: A novel approach for the prevention and treatment of Type 2 diabetes
-
Deacon, C. F, Ahrén, B., Holst, J. J.: Inhibition of dipeptidyl peptidase IV: a novel approach for the prevention and treatment of Type 2 diabetes. Exp. Opin. Invest. Drugs, 2004, 13, 1091-1102.
-
(2004)
Exp. Opin. Invest. Drugs
, vol.13
, pp. 1091-1102
-
-
Deacon, C.F.1
Ahrén, B.2
Holst, J.J.3
-
26
-
-
33750914846
-
Exendin 4 controls insulin production in rat islet beta cells predominantly by potentiation of glucose-stimulated proinsulin biosynthesis at the translational level
-
Alarcon, C., Wicksteed, B., Rhodes, C. J.: Exendin 4 controls insulin production in rat islet beta cells predominantly by potentiation of glucose-stimulated proinsulin biosynthesis at the translational level. Diabetologia, 2006, 49, 2920-2929.
-
(2006)
Diabetologia
, vol.49
, pp. 2920-2929
-
-
Alarcon, C.1
Wicksteed, B.2
Rhodes, C.J.3
-
27
-
-
33644819643
-
Exendin-4, but not glucagon-like peptide-1, is cleared exclusively by glomerular filtration in anaesthetised pigs
-
Simonsen, L., Holst, J. J., Deacon, C. F.: Exendin-4, but not glucagon-like peptide-1, is cleared exclusively by glomerular filtration in anaesthetised pigs. Diabetologia, 2006, 49, 706-712.
-
(2006)
Diabetologia
, vol.49
, pp. 706-712
-
-
Simonsen, L.1
Holst, J.J.2
Deacon, C.F.3
-
28
-
-
2342599057
-
-
Degn, K. B. J., Sturis, C. B., Jakobsen, J. és mtsai: One week's treatment with the long-acting glucagon-like peptide 1 derivative liraglutide (NN2211) markedly improves 24-h glycemia and alpha- and beta-cell function and reduces endogenous glucose release in patients with type 2 diabetes. Diabetes, 2004, 53, 1187-1194.
-
Degn, K. B. J., Sturis, C. B., Jakobsen, J. és mtsai: One week's treatment with the long-acting glucagon-like peptide 1 derivative liraglutide (NN2211) markedly improves 24-h glycemia and alpha- and beta-cell function and reduces endogenous glucose release in patients with type 2 diabetes. Diabetes, 2004, 53, 1187-1194.
-
-
-
-
29
-
-
32844473903
-
-
Bergman, A. J., Stevens, C., Zhou, Y. Y. és mtsai: Pharmacokinetic and pharmacodynamic properties of multiple oral doses of sitagliptin, a dipeptidyl peptidase-IV inhibitor: a double-blind randomized, placebo-controlled study in healthy male volunteers. Clin. Ther., 2006, 28, 55-72.
-
Bergman, A. J., Stevens, C., Zhou, Y. Y. és mtsai: Pharmacokinetic and pharmacodynamic properties of multiple oral doses of sitagliptin, a dipeptidyl peptidase-IV inhibitor: a double-blind randomized, placebo-controlled study in healthy male volunteers. Clin. Ther., 2006, 28, 55-72.
-
-
-
-
30
-
-
19944427998
-
-
Kim, D., Wang, L., Beconi, M. és mtsai: (2R)-4-oxo-4 [3-(trifluoromethyl)-5,6-dihydro/1,2,4/triazolo/4,3-a/pyrazin-7 (8H)-yl-] 1-(2,4,5-trifluorophenyl)butan-2-amine: a potent, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. J. Med. Chem., 2005, 48, 141-151.
-
Kim, D., Wang, L., Beconi, M. és mtsai: (2R)-4-oxo-4 [3-(trifluoromethyl)-5,6-dihydro/1,2,4/triazolo/4,3-a/pyrazin-7 (8H)-yl-] 1-(2,4,5-trifluorophenyl)butan-2-amine: a potent, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. J. Med. Chem., 2005, 48, 141-151.
-
-
-
-
31
-
-
25844459084
-
-
Lankas, G. R., Leiting, B., Roy, B. S. és mtsai: Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes. Potential importance of selectivity over dipeptidyl peptidases 8 and 9. Diabetes, 2005, 54, 2988-2994.
-
Lankas, G. R., Leiting, B., Roy, B. S. és mtsai: Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes. Potential importance of selectivity over dipeptidyl peptidases 8 and 9. Diabetes, 2005, 54, 2988-2994.
-
-
-
-
32
-
-
33745909432
-
-
Herman, G. A, Bergman, A., Liu, F. és mtsai: Pharmacokinetics and pharmacodynamic effects of the oral DPP-4 inhibitor sitagliptin in middle-aged obese subjects. J. Clin. Pharmacol., 2006, 46, 876-886.
-
Herman, G. A, Bergman, A., Liu, F. és mtsai: Pharmacokinetics and pharmacodynamic effects of the oral DPP-4 inhibitor sitagliptin in middle-aged obese subjects. J. Clin. Pharmacol., 2006, 46, 876-886.
-
-
-
-
33
-
-
33845489598
-
-
Raz, I., Hanefeld, M., Xu, L. és mtsai (for the Sitagliptin Study 023 Group): Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy in patients with type 2 diabetes mellitus. Diabetologia, 2006, 49, 2564-2571.
-
Raz, I., Hanefeld, M., Xu, L. és mtsai (for the Sitagliptin Study 023 Group): Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy in patients with type 2 diabetes mellitus. Diabetologia, 2006, 49, 2564-2571.
-
-
-
-
34
-
-
33745780301
-
-
Nathan, D. M, Buse, J. B., Davidson, M. B. és mtsai: Management of chronic hyperglycaemia in type 2 diabetes: a consensus algorithm for the initiation and adjustment of therapy. A consensus statement from the American Diabetes Association and the European Association for the Study of Diabetes. Diabetologia, 2006, 49, 1711-1721.
-
Nathan, D. M, Buse, J. B., Davidson, M. B. és mtsai: Management of chronic hyperglycaemia in type 2 diabetes: a consensus algorithm for the initiation and adjustment of therapy. A consensus statement from the American Diabetes Association and the European Association for the Study of Diabetes. Diabetologia, 2006, 49, 1711-1721.
-
-
-
-
35
-
-
33751557143
-
J. és mtsai (for the Sitagliptin Study 019 Group): Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagliptin added to ongoing pioglitazone therapy in patients with type 2 diabetes: a 24-week, multicenter, randomized, double-blind, placebo-controlled, parallel-group study
-
Rosenstock, J., Brazg, R., Andryuk, P. J. és mtsai (for the Sitagliptin Study 019 Group): Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagliptin added to ongoing pioglitazone therapy in patients with type 2 diabetes: a 24-week, multicenter, randomized, double-blind, placebo-controlled, parallel-group study. Clin. Ther., 2006, 28, 1556-1568.
-
(2006)
Clin. Ther
, vol.28
, pp. 1556-1568
-
-
Rosenstock, J.1
Brazg, R.2
Andryuk, P.3
-
36
-
-
33751098267
-
Vildaliptin
-
Henness, S., Keam, S. J.: Vildaliptin. Drugs, 2006, 66, 1989-2001.
-
(2006)
Drugs
, vol.66
, pp. 1989-2001
-
-
Henness, S.1
Keam, S.J.2
-
37
-
-
20444406121
-
-
Brandt, L, Joossens, J., Chen, X. és mtsai: Inhibition of dipeptidyl-peptidase IV catalyzed peptide truncation oy vildagliptin ((2S- [(3-hydroxyadamantan- 1-yl)amino]acetyl-pyrrolidine-2-carbonitrile). Biochem. Pharmacol., 2005, 70, 134-143.
-
Brandt, L, Joossens, J., Chen, X. és mtsai: Inhibition of dipeptidyl-peptidase IV catalyzed peptide truncation oy vildagliptin ((2S- [(3-hydroxyadamantan- 1-yl)amino]acetyl-pyrrolidine-2-carbonitrile). Biochem. Pharmacol., 2005, 70, 134-143.
-
-
-
-
38
-
-
84873213325
-
-
Mari, A., Sallas, W. M., He, Y. L. és mtsai: Vildagliptin, a dipeptidyl peptidase-IV inhibitor, improves model-assessed β-cell function in patients with type 2 diabetes. J. Clin. Endocrinol. Metab., 2005, 90, 4858-4864.
-
Mari, A., Sallas, W. M., He, Y. L. és mtsai: Vildagliptin, a dipeptidyl peptidase-IV inhibitor, improves model-assessed β-cell function in patients with type 2 diabetes. J. Clin. Endocrinol. Metab., 2005, 90, 4858-4864.
-
-
-
-
39
-
-
27744540889
-
J. és mtsai: Improved glycaemic control with dipeptidyl peptidase-4 inhibition in patients with type 2 diabetes: vildaghptin (LAF237) dose response
-
Ristic, S., Byiers, S., Foley, J. és mtsai: Improved glycaemic control with dipeptidyl peptidase-4 inhibition in patients with type 2 diabetes: vildaghptin (LAF237) dose response. Diab. Obes. Metab., 2005, 7, 692-698.
-
(2005)
Diab. Obes. Metab
, vol.7
, pp. 692-698
-
-
Ristic, S.1
Byiers, S.2
Foley3
-
40
-
-
9444285818
-
-
Ahrén, B., Gomis, R., Standl, E. és mtsai: Twelve- and 52-week efficacy of the dipeptidyl peptidase IV inhibitor LAF237 in metformin-treated patients with type 2 diabetes. Diabetes Care, 2004, 27, 2874-2880.
-
Ahrén, B., Gomis, R., Standl, E. és mtsai: Twelve- and 52-week efficacy of the dipeptidyl peptidase IV inhibitor LAF237 in metformin-treated patients with type 2 diabetes. Diabetes Care, 2004, 27, 2874-2880.
-
-
-
-
41
-
-
2442482515
-
P-A. és mtsai: Inhibition of dipeptidy peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes
-
Ahrén, B., Landin-Olsson, M., Jansson, P-A. és mtsai: Inhibition of dipeptidy peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes. J. Clin. Endocr. Metab., 2004, 89, 2078-2084.
-
(2004)
J. Clin. Endocr. Metab
, vol.89
, pp. 2078-2084
-
-
Ahrén, B.1
Landin-Olsson, M.2
Jansson3
-
42
-
-
0033619675
-
Dipeptidyl-peptidase IV (CD26)-role in the inactivation of regulatory peptides
-
Mentlein, R.: Dipeptidyl-peptidase IV (CD26)-role in the inactivation of regulatory peptides. Regul. Pept., 1999, 85, 9-24.
-
(1999)
Regul. Pept
, vol.85
, pp. 9-24
-
-
Mentlein, R.1
-
43
-
-
21244495238
-
The incretin effect and its potentiation by glucagon-like peptide-l-based therapies: A revolution in diabetes management
-
Roges, O. A., Baron, M., Philis-Tsimikas, A.: The incretin effect and its potentiation by glucagon-like peptide-l-based therapies: a revolution in diabetes management. Exp. Opin. Investig. Drugs, 2005, 14, 705-727.
-
(2005)
Exp. Opin. Investig. Drugs
, vol.14
, pp. 705-727
-
-
Roges, O.A.1
Baron, M.2
Philis-Tsimikas, A.3
-
44
-
-
7444228521
-
-
Buse, J. B, Henry, R. R., Chan, J. és mtsai (for the Exenatide-113 Clinical Study Group): Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-patients with type 2 diabetes. Diabetes Care, 2004, 27, 2628-2635.
-
Buse, J. B, Henry, R. R., Chan, J. és mtsai (for the Exenatide-113 Clinical Study Group): Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-patients with type 2 diabetes. Diabetes Care, 2004, 27, 2628-2635.
-
-
-
-
45
-
-
18144401971
-
-
DeFronzo, R. A., Rainer, R. E., Han, J. és mtsai: Effects of exenatide (exendin-4) on glycemic control and weight gain over 30 weeks in metformin-treated patients with type 2 diabetes. Diabetes Care, 2005, 28, 1092-1100.
-
DeFronzo, R. A., Rainer, R. E., Han, J. és mtsai: Effects of exenatide (exendin-4) on glycemic control and weight gain over 30 weeks in metformin-treated patients with type 2 diabetes. Diabetes Care, 2005, 28, 1092-1100.
-
-
-
-
46
-
-
33748442464
-
J. és mtsai: Interim analysis of the effects of exenatide treatment on Alc, weight and cardiovascular risk factors over 82 weeks in 314 overweight patients with type 2 diabetes
-
Blonde, L., Klein, E. J., Han, J. és mtsai: Interim analysis of the effects of exenatide treatment on Alc, weight and cardiovascular risk factors over 82 weeks in 314 overweight patients with type 2 diabetes. Diab. Obes. Metab., 2006, 8, 436-447.
-
(2006)
Diab. Obes. Metab
, vol.8
, pp. 436-447
-
-
Blonde, L.1
Klein, E.2
Han, J.3
-
47
-
-
26944477362
-
J. és mtsai (for the GWAA Study Group): Exenatide versus insulin glargine in patients with suboptimally controlled type 2 diabetes
-
Heine, R., Van Gaal, L. F., Mibm, M. J. és mtsai (for the GWAA Study Group): Exenatide versus insulin glargine in patients with suboptimally controlled type 2 diabetes. Ann. Intern. Med., 2005, 143, 559-569.
-
(2005)
Ann. Intern. Med
, vol.143
, pp. 559-569
-
-
Heine, R.1
Van Gaal, L.F.2
Mibm, M.3
-
48
-
-
34247195226
-
-
Nauck, M. A., Duran, S., Kim, D. és mtsai: A comparison of twice-daily exenatide and biphasic insulin aspart in patients suboptimally controlled with sulfonylurea and metformin: a non-inferiority study. Diabetologia, 2007, 50, 259-267.
-
Nauck, M. A., Duran, S., Kim, D. és mtsai: A comparison of twice-daily exenatide and biphasic insulin aspart in patients suboptimally controlled with sulfonylurea and metformin: a non-inferiority study. Diabetologia, 2007, 50, 259-267.
-
-
-
-
49
-
-
34848849278
-
Exenatid a klinikai gyakorlatban. Hosszabb távú alkalmazásának tapasztalatai 2-es típusú diabetesben, irodalmi áttekintés alapján
-
Winkler, G.: Exenatid a klinikai gyakorlatban. Hosszabb távú alkalmazásának tapasztalatai 2-es típusú diabetesben, irodalmi áttekintés alapján. Diabetol. Hung., 2006, 14 (Suppl. 4), 5-12.
-
(2006)
Diabetol. Hung
, vol.14
, Issue.SUPPL. 4
, pp. 5-12
-
-
Winkler, G.1
-
50
-
-
14644435731
-
-
Petersen, K. F., Dufour, S., Befroy, D. és mtsai: Reversal of nonalcoholic hepatic steatosis, hepatic insulin resistance, and hyperglycemia by moderate weight reduction in patients with type 2 diabetes. Diabetes, 2005, 54, 603-608.
-
Petersen, K. F., Dufour, S., Befroy, D. és mtsai: Reversal of nonalcoholic hepatic steatosis, hepatic insulin resistance, and hyperglycemia by moderate weight reduction in patients with type 2 diabetes. Diabetes, 2005, 54, 603-608.
-
-
-
|