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Items: 1 to 20 of 39


Metabolically healthy obese women have longer telomere length than obese women with metabolic syndrome.

Iglesias Molli AE, Panero J, Dos Santos PC, González CD, Vilariño J, Sereday M, Cerrone GE, Slavutsky I, Frechtel GD.

PLoS One. 2017 Apr 6;12(4):e0174945. doi: 10.1371/journal.pone.0174945. eCollection 2017.


NETosis before and after Hyperglycemic Control in Type 2 Diabetes Mellitus Patients.

Carestia A, Frechtel G, Cerrone G, Linari MA, Gonzalez CD, Casais P, Schattner M.

PLoS One. 2016 Dec 22;11(12):e0168647. doi: 10.1371/journal.pone.0168647. eCollection 2016.


The effects of exenatide twice daily compared to insulin lispro added to basal insulin in Latin American patients with type 2 diabetes: A retrospective analysis of the 4B trial.

de Lapertosa SB, Frechtel G, Hardy E, Sauque-Reyna L.

Diabetes Res Clin Pract. 2016 Dec;122:38-45. doi: 10.1016/j.diabres.2016.10.001. Epub 2016 Oct 8.


Use of cross-reactivity immunoassay to orient insulin replacement in diabetic patients with high levels of insulin antibodies.

Cardoso Landaburu A, Pomares M, Avalos A, Lapertosa S, Frechtel G, Poskus E.

MethodsX. 2016 Aug 5;3:502-7. doi: 10.1016/j.mex.2016.08.003. eCollection 2016.


Challenges associated with insulin therapy progression among patients with type 2 diabetes: Latin American MOSAIc study baseline data.

Linetzky B, Curtis B, Frechtel G, Montenegro R Jr, Escalante Pulido M, Stempa O, de Lana JM, Gagliardino JJ.

Diabetol Metab Syndr. 2016 Jul 22;8:41. doi: 10.1186/s13098-016-0157-1. eCollection 2016.


Analysis of mutations in the glucokinase gene in people clinically characterized as MODY2 without a family history of diabetes.

Lopez AP, de Dios A, Chiesa I, Perez MS, Frechtel GD.

Diabetes Res Clin Pract. 2016 Aug;118:38-43. doi: 10.1016/j.diabres.2016.04.057. Epub 2016 May 26.


Characterization of zinc transporter 8 (ZnT8) antibodies in autoimmune diabetic patients from Argentinian population using monomeric, homodimeric, and heterodimeric ZnT8 antigen variants.

Faccinetti NI, Guerra LL, Penas Steinhardt A, Iacono RF, Frechtel GD, Trifone L, Poskus E, Trabucchi A, Valdez SN.

Eur J Endocrinol. 2016 Feb;174(2):157-65. doi: 10.1530/EJE-15-0681. Epub 2015 Nov 13.


Saxagliptin and cardiovascular outcomes in patients with type 2 diabetes mellitus.

Scirica BM, Bhatt DL, Braunwald E, Steg PG, Davidson J, Hirshberg B, Ohman P, Frederich R, Wiviott SD, Hoffman EB, Cavender MA, Udell JA, Desai NR, Mosenzon O, McGuire DK, Ray KK, Leiter LA, Raz I; SAVOR-TIMI 53 Steering Committee and Investigators..

N Engl J Med. 2013 Oct 3;369(14):1317-26. doi: 10.1056/NEJMoa1307684. Epub 2013 Sep 2.


Functional characterization of TLR4 +3725 G/C polymorphism and association with protection against overweight.

Penas-Steinhardt A, Barcos LS, Belforte FS, de Sereday M, Vilariño J, Gonzalez CD, Martínez-Larrad MT, Tellechea ML, Serrano-Ríos M, Poskus E, Frechtel GD, Leskow FC.

PLoS One. 2012;7(12):e50992. doi: 10.1371/journal.pone.0050992. Epub 2012 Dec 11.


Association between β2-adrenoceptor (ADRB2) haplotypes and insulin resistance in PCOS.

Tellechea ML, Muzzio DO, Iglesias Molli AE, Belli SH, Graffigna MN, Levalle OA, Frechtel GD, Cerrone GE.

Clin Endocrinol (Oxf). 2013 Apr;78(4):600-6. doi: 10.1111/cen.12019.


Common variants in SOCS7 gene predict obesity, disturbances in lipid metabolism and insulin resistance.

Tellechea ML, Steinhardt AP, Rodriguez G, Taverna MJ, Poskus E, Frechtel G.

Nutr Metab Cardiovasc Dis. 2013 May;23(5):424-31. doi: 10.1016/j.numecd.2011.10.005. Epub 2012 Mar 6.


Association of common variants in JAK2 gene with reduced risk of metabolic syndrome and related disorders.

Penas-Steinhardt A, Tellechea ML, Gomez-Rosso L, Brites F, Frechtel GD, Poskus E.

BMC Med Genet. 2011 Dec 20;12:166. doi: 10.1186/1471-2350-12-166.


Design, history and results of the Thiazolidinedione Intervention with vitamin D Evaluation (TIDE) randomised controlled trial.

Punthakee Z, Bosch J, Dagenais G, Diaz R, Holman R, Probstfield J, Ramachandran A, Riddle M, Rydén LE, Zinman B, Afzal R, Yusuf S, Gerstein H; TIDE Trial Investigators..

Diabetologia. 2012 Jan;55(1):36-45. doi: 10.1007/s00125-011-2357-4. Epub 2011 Oct 29.


Detection and characterization of ZnT8 autoantibodies could help to screen latent autoimmune diabetes in adult-onset patients with type 2 phenotype.

Trabucchi A, Faccinetti NI, Guerra LL, Puchulu FM, Frechtel GD, Poskus E, Valdez SN.

Autoimmunity. 2012 Mar;45(2):137-42. doi: 10.3109/08916934.2011.604658. Epub 2011 Aug 30.


The rs1801278 G>A polymorphism of IRS-1 is associated with metabolic syndrome in healthy nondiabetic men. Modulation by cigarette smoking status.

Pérez MS, Tellechea ML, Aranguren F, Taverna MJ, Rodríguez RG, Meroño T, Brites F, Poskus E, Frechtel GD.

Diabetes Res Clin Pract. 2011 Sep;93(3):e95-7. doi: 10.1016/j.diabres.2011.05.018. Epub 2011 Jun 8.


Treatment of type 2 diabetes in Latin America: a consensus statement by the medical associations of 17 Latin American countries. Latin American Diabetes Association.

Guzmán JR, Lyra R, Aguilar-Salinas CA, Cavalcanti S, Escaño F, Tambasia M, Duarte E; ALAD Consensus Group..

Rev Panam Salud Publica. 2010 Dec;28(6):463-71.


Lipid accumulation product: a powerful marker of metabolic syndrome in healthy population.

Taverna MJ, Martínez-Larrad MT, Frechtel GD, Serrano-Ríos M.

Eur J Endocrinol. 2011 Apr;164(4):559-67. doi: 10.1530/EJE-10-1039. Epub 2011 Jan 24. Erratum in: Eur J Endocrinol. 2011 May;164(5):849.


HNF1 alpha gene coding regions mutations screening, in a Caucasian population clinically characterized as MODY from Argentina.

Lopez AP, Foscaldi SA, Perez MS, Rodriguez M, Traversa M, Puchulu FM, Bergada I, Frechtel GD.

Diabetes Res Clin Pract. 2011 Feb;91(2):208-12. doi: 10.1016/j.diabres.2010.11.024. Epub 2010 Dec 17.


A functional nonsynonymous toll-like receptor 4 gene polymorphism is associated with metabolic syndrome, surrogates of insulin resistance, and syndromes of lipid accumulation.

Steinhardt AP, Aranguren F, Tellechea ML, Gómez Rosso LA, Brites FD, Martínez-Larrad MT, Serrano-Ríos M, Frechtel GD, Taverna MJ.

Metabolism. 2010 May;59(5):711-7. doi: 10.1016/j.metabol.2009.09.015. Epub 2009 Nov 18.


GJB2 and GJB6 genes: molecular study and identification of novel GJB2 mutations in the hearing-impaired Argentinean population.

Dalamón V, Lotersztein V, Béhèran A, Lipovsek M, Diamante F, Pallares N, Francipane L, Frechtel G, Paoli B, Mansilla E, Diamante V, Elgoyhen AB.

Audiol Neurootol. 2010;15(3):194-202. doi: 10.1159/000254487. Epub 2009 Nov 4.


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