Frechtel GD - Search Results

1

Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion.

Ferreiro V, Giliberto F, Muñiz GM, Francipane L, Marzese DM, Mampel A, Roqué M, Frechtel GD, Szijan I. Ferreiro V, et al. Among authors: frechtel gd. Muscle Nerve. 2009 Feb;39(2):239-43. doi: 10.1002/mus.21193. Muscle Nerve. 2009. PMID: 19012301

2

Advancing therapy in people with suboptimally controlled basal insulin-treated type 2 diabetes: Subanalysis of the SoliMix trial in participants in Latin American countries.

Frechtel G, Sauque-Reyna L, Choza-Romero R, Anguiano L, Melas-Melt L, Sañudo-Maury ME. Frechtel G, et al. Diabetes Obes Metab. 2023 Sep;25(9):2526-2534. doi: 10.1111/dom.15125. Epub 2023 May 30. Diabetes Obes Metab. 2023. PMID: 37253689 Clinical Trial.

3

Supernumerary marker 15 chromosome in a patient with Prader-Willi syndrome.

Borelina D, Esperante S, Gutnisky V, Ferreiro V, Ferrer M, Giliberto F, Frechtel G, Francipane L, Szijan I. Borelina D, et al. Clin Genet. 2004 Mar;65(3):242-3. doi: 10.1111/j.0009-9163.2004.00203.x. Clin Genet. 2004. PMID: 14756675 No abstract available.

4

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. Dalamón V, et al. Audiol Neurootol. 2010;15(3):194-202. doi: 10.1159/000254487. Epub 2009 Nov 4. Audiol Neurootol. 2010. PMID: 19887791

5

A novel mutation in exon 5 of the glucokinase gene in an Argentinian family with maturity onset diabetes of the young.

Frechtel GD, López AP, Rodríguez M, Cerrone GE, Targovnik HM. Frechtel GD, et al. Mol Diagn. 2003;7(2):129-31. doi: 10.1007/BF03260029. Mol Diagn. 2003. PMID: 14580233

6

Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidism.

Targovnik HM, Frechtel GD, Mendive FM, Vono J, Cochaux P, Vassart G, Medeiros-Neto G. Targovnik HM, et al. Among authors: frechtel gd. Thyroid. 1998 Apr;8(4):291-7. doi: 10.1089/thy.1998.8.291. Thyroid. 1998. PMID: 9588493

7

17alpha-hydroxylase deficiency : biochemical and molecular findings in two sisters and their family.

Perez MS, Benencia H, Frechtel GD, Esteban EO, Gil MC, Targovnik HM, Marquez NB. Perez MS, et al. Among authors: frechtel gd. Mol Diagn. 2004;8(3):171-8. doi: 10.1007/BF03260061. Mol Diagn. 2004. PMID: 15771555

8

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. Lopez AP, et al. Among authors: frechtel gd. Diabetes Res Clin Pract. 2016 Aug;118:38-43. doi: 10.1016/j.diabres.2016.04.057. Epub 2016 May 26. Diabetes Res Clin Pract. 2016. PMID: 27289208

9

Glucokinase gene mutation screening in Argentinean clinically characterized MODY patients.

Lopez AP, Foscaldi SA, Pérez MS, Krochik G, Rodríguez M, Traversa M, Puchulu FM, Hirschler V, Bergada I, Frechtel GD. Lopez AP, et al. Among authors: frechtel gd. Exp Clin Endocrinol Diabetes. 2009 Sep;117(8):391-4. doi: 10.1055/s-0029-1214427. Epub 2009 Apr 8. Exp Clin Endocrinol Diabetes. 2009. PMID: 19358091

10

Pro12Ala polymorphism of the peroxisome proliferatoractivated receptor-gamma gene is associated with metabolic syndrome and surrogate measures of insulin resistance in healthy men: interaction with smoking status.

Tellechea ML, Aranguren F, Pérez MS, Cerrone GE, Frechtel GD, Taverna MJ. Tellechea ML, et al. Among authors: frechtel gd. Circ J. 2009 Nov;73(11):2118-24. doi: 10.1253/circj.cj-09-0320. Epub 2009 Sep 10. Circ J. 2009. PMID: 19745552 Free article.

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