Frechtel GD - Search Results

1

Cytotoxic T lymphocyte antigen 4 heterozygous codon 49 A/G dimorphism is associated to latent autoimmune diabetes in adults (LADA).

Caputo M, Cerrone GE, López AP, Villalba A, Krochik GA, Cédola FN, Targovnik HM, Frechtel GD. Caputo M, et al. Among authors: frechtel gd. Autoimmunity. 2005 Jun;38(4):277-81. doi: 10.1080/08916930500158203. Autoimmunity. 2005. PMID: 16206510 Free article.

2

Differential levels of thyroid peroxidase and thyroglobulin messenger ribonucleic acids in congenital goiter with defective thyroglobulin synthesis.

Targovnik HM, Varela V, Juvenal GJ, Propato F, Chester HA, Krawiec L, Frechtel G, Moran DH, Perinetti HA, Pisarev MA. Targovnik HM, et al. J Endocrinol Invest. 1990 Nov;13(10):797-806. doi: 10.1007/BF03349625. J Endocrinol Invest. 1990. PMID: 2096156

3

Molecular genetics of hereditary thyroid diseases due to a defect in the thyroglobulin or thyroperoxidase synthesis.

Targovnik HM, Varela V, Frechtel GD, Cerrone GE, Copelli SB, Propato FV, Mendive F. Targovnik HM, et al. Among authors: frechtel gd. Braz J Med Biol Res. 1994 Dec;27(12):2745-57. Braz J Med Biol Res. 1994. PMID: 7549998 Review.

4

Human thyroid tissue do not express thyroalbumin.

Targovnik HM, Frechtel GD, Varela V, Wajchenberg BL, Vassart G, Dumont J, Medeiros-Neto GA. Targovnik HM, et al. Among authors: frechtel gd. J Endocrinol Invest. 1993 Jun;16(6):415-9. doi: 10.1007/BF03348869. J Endocrinol Invest. 1993. PMID: 8370916

5

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

6

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

7

Variable number of tandem repeats of the insulin gene determines susceptibility to latent autoimmune diabetes in adults.

Cerrone GE, Caputo M, Lopez AP, González C, Massa C, Cédola N, Targovnik HM, Frechtel GD. Cerrone GE, et al. Among authors: frechtel gd. Mol Diagn. 2004;8(1):43-9. doi: 10.1007/BF03260046. Mol Diagn. 2004. PMID: 15230641

8

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

9

[HLA DQB1 genotyping in latent autoimmune diabetes of adults (LADA)].

Caputo M, Cerrone GE, Lopez AP, Gonzalez C, Mazza C, Cedola N, Puchulu FM, Targovnik HM, Frechtel GD. Caputo M, et al. Among authors: frechtel gd. Medicina (B Aires). 2005;65(3):235-40. Medicina (B Aires). 2005. PMID: 16042135 Spanish.

10

A simple method for the identification of three major haplotypes of the beta2AR.

Cerrone GE, Pérez MS, Caputo M, Targovnik HM, Frechtel GD. Cerrone GE, et al. Among authors: frechtel gd. Mol Cell Probes. 2007 Jun;21(3):222-5. doi: 10.1016/j.mcp.2006.12.004. Epub 2007 Jan 12. Mol Cell Probes. 2007. PMID: 17303378

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