Targovnik HM - Search Results

1

Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect.

Rivolta CM, Esperante SA, Gruñeiro-Papendieck L, Chiesa A, Moya CM, Domené S, Varela V, Targovnik HM. Rivolta CM, et al. Among authors: targovnik hm. Hum Mutat. 2003 Sep;22(3):259. doi: 10.1002/humu.9175. Hum Mutat. 2003. PMID: 12938097

2

Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.

Abramowicz MJ, Targovnik HM, Varela V, Cochaux P, Krawiec L, Pisarev MA, Propato FV, Juvenal G, Chester HA, Vassart G. Abramowicz MJ, et al. Among authors: targovnik hm. J Clin Invest. 1992 Oct;90(4):1200-4. doi: 10.1172/JCI115981. J Clin Invest. 1992. PMID: 1401057 Free PMC article.

3

Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis.

Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros-Neto G. Targovnik HM, et al. Thyroid. 1991 Winter;1(4):339-45. doi: 10.1089/thy.1991.1.339. Thyroid. 1991. PMID: 1726786

4

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

5

Low levels of thyroglobulin messenger ribonucleic acid in congenital goitrous hypothyroidism with defective thyroglobulin synthesis.

Targovnik H, Propato F, Varela V, Wajchenberg B, Knobel M, D'Abronzo HF, Medeiros-Neto G. Targovnik H, et al. J Clin Endocrinol Metab. 1989 Dec;69(6):1137-47. doi: 10.1210/jcem-69-6-1137. J Clin Endocrinol Metab. 1989. PMID: 2584351

6

Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter. Absence of gross gene deletion of coding sequences in the TG gene structure.

Medeiros-Neto G, Targovnik H, Knobel M, Propato F, Varela V, Alkmin M, Barbosa S, Wajchenberg BL. Medeiros-Neto G, et al. J Endocrinol Invest. 1989 Dec;12(11):805-13. doi: 10.1007/BF03350067. J Endocrinol Invest. 1989. PMID: 2614017

7

Inhibitory action of dipyrone on rat thyroid peroxidase and lactoperoxidase activities.

Varela V, del Valle Paz CV, Houssay AB, Targovnik HM. Varela V, et al. Among authors: targovnik hm. Acta Physiol Pharmacol Latinoam. 1985;35(2):259-66. Acta Physiol Pharmacol Latinoam. 1985. PMID: 2938410

8

Effects of indomethacin on thyroid iodine metabolism.

Targovnik HM, Varela V, Houssay AB, Paz C, Cohen Saban H. Targovnik HM, et al. Acta Physiol Lat Am. 1983;33(4):327-34. Acta Physiol Lat Am. 1983. PMID: 6678104

9

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. Braz J Med Biol Res. 1994 Dec;27(12):2745-57. Braz J Med Biol Res. 1994. PMID: 7549998 Review.

10

A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis.

Targovnik HM, Vono J, Billerbeck AE, Cerrone GE, Varela V, Mendive F, Wajchenberg BL, Medeiros-Neto G. Targovnik HM, et al. J Clin Endocrinol Metab. 1995 Nov;80(11):3356-60. doi: 10.1210/jcem.80.11.7593451. J Clin Endocrinol Metab. 1995. PMID: 7593451

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