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Results: 1-18 |
Results: 18
Searching for iodine deficiency disorders in schoolchildren from Brazil: The Thyromobil project
Authors: Rossi, AC Tomimori, E Camargo, R Medeiros-Neto, G
Citation: Ac. Rossi et al., Searching for iodine deficiency disorders in schoolchildren from Brazil: The Thyromobil project, THYROID, 11(7), 2001, pp. 661-663
Congenital goiter with hypothyroidism caused by a 5 ' splice site mutationin the thyroglobulin gene
Authors: Targovnik, HM Rivolta, CM Mendive, FM Moya, CM Vono, J Medeiros-Neto, G
Citation: Hm. Targovnik et al., Congenital goiter with hypothyroidism caused by a 5 ' splice site mutationin the thyroglobulin gene, THYROID, 11(7), 2001, pp. 685-690
Aggressive metastatic follicular thyroid carcinoma with anaplastic transformation arising from a long-standing goiter in a patient with Pendred's syndrome
Authors: Camargo, R Limbert, E Gillam, M Henriques, MM Fernandes, C Catarino, AL Soares, J Alves, VAF Kopp, P Medeiros-Neto, G
Citation: R. Camargo et al., Aggressive metastatic follicular thyroid carcinoma with anaplastic transformation arising from a long-standing goiter in a patient with Pendred's syndrome, THYROID, 11(10), 2001, pp. 981-988
Overexpression of epidermal growth factor and epidermal growth factor-receptor mRNAs in dyshormonogenetic goiters
Authors: Pedrinola, F Rubio, I Santos, CLS Medeiros-Neto, G
Citation: F. Pedrinola et al., Overexpression of epidermal growth factor and epidermal growth factor-receptor mRNAs in dyshormonogenetic goiters, THYROID, 11(1), 2001, pp. 15-20
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
Authors: Trevino, OG Arseven, OK Ceballos, CJ Vives, VI Ramirez, RC Gomez, VV Medeiros-Neto, G Kopp, P
Citation: Og. Trevino et al., Clinical and molecular analysis of three Mexican families with Pendred's syndrome, EUR J ENDOC, 144(6), 2001, pp. 585-593
Gastrointestinal side effects of orlistat may be prevented by concomitant prescription of natural fibers (psyllium mucilloid)
Authors: Cavaliere, H Floriano, I Medeiros-Neto, G
Citation: H. Cavaliere et al., Gastrointestinal side effects of orlistat may be prevented by concomitant prescription of natural fibers (psyllium mucilloid), INT J OBES, 25(7), 2001, pp. 1095-1099
A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: Evidence for phenotypic variability in mother and child
Authors: Congdon, T Nguyen, LQ Nogueira, CR Habiby, RL Medeiros-Neto, G Kopp, P
Citation: T. Congdon et al., A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: Evidence for phenotypic variability in mother and child, J CLIN END, 86(8), 2001, pp. 3962-3967
Thyroid in the third millennium: Quo vadis?
Authors: Medeiros-Neto, G
Citation: G. Medeiros-neto, Thyroid in the third millennium: Quo vadis?, THYROID, 10(3), 2000, pp. 227-227
Decreased androgen levels in massively obese men may be associated with impaired function of the gonadostat
Authors: Lima, N Cavaliere, H Knobel, M Halpern, A Medeiros-Neto, G
Citation: N. Lima et al., Decreased androgen levels in massively obese men may be associated with impaired function of the gonadostat, INT J OBES, 24(11), 2000, pp. 1433-1437
Prevalence and characteristics of postpartum thyroid dysfunction in Sao Paulo, Brazil
Authors: Barca, MF Knobel, M Tomimori, E Cardia, MS Medeiros-Neto, G
Citation: Mf. Barca et al., Prevalence and characteristics of postpartum thyroid dysfunction in Sao Paulo, Brazil, CLIN ENDOCR, 53(1), 2000, pp. 21-31
Combined pituitary hormone deficiency in an inbred Brazilian kindred associated with a mutation in the PROP-1 gene
Authors: Nogueira, CR Sabacan, L Jameson, JL Medeiros-Neto, G Kopp, P
Citation: Cr. Nogueira et al., Combined pituitary hormone deficiency in an inbred Brazilian kindred associated with a mutation in the PROP-1 gene, MOL GEN MET, 67(1), 1999, pp. 58-61
Elevated anti-galactosyl antibody titers in endemic goiter
Authors: Knobel, M Umezawa, ES Cardia, MS Martins, MJT Correa, MLC Gianella-Neto, D Caulier, C Medeiros-Neto, G
Citation: M. Knobel et al., Elevated anti-galactosyl antibody titers in endemic goiter, THYROID, 9(5), 1999, pp. 493-498
Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil
Authors: Nogueira, CR Kopp, P Arseven, OK Santos, CLS Jameson, JL Medeiros-Neto, G
Citation: Cr. Nogueira et al., Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil, THYROID, 9(11), 1999, pp. 1063-1068
Combined ultrasonographic and cytological studies in the diagnosis of thyroid nodules
Authors: Tomimori, EK Camargo, RYA Bisi, H Medeiros-Neto, G
Citation: Ek. Tomimori et al., Combined ultrasonographic and cytological studies in the diagnosis of thyroid nodules, BIOCHIMIE, 81(5), 1999, pp. 447-452
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect
Authors: Santos, CLS Bikker, H Rego, KGM Nascimento, AC Tambascia, M de Vijlder, JJM Medeiros-Neto, G
Citation: Cls. Santos et al., A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect, CLIN ENDOCR, 51(2), 1999, pp. 165-172
A premature stopcodon in thyroglobulin messenger RNA results in familial goiter and moderate hypothyroidism
Authors: van de Graaf, SAR Ris-Stalpers, C Veenboer, GJM Cammenga, M Santos, C Targovnik, HM De Vijlder, JJM Medeiros-Neto, G
Citation: Sar. Van De Graaf et al., A premature stopcodon in thyroglobulin messenger RNA results in familial goiter and moderate hypothyroidism, J CLIN END, 84(7), 1999, pp. 2537-2542
Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene
Authors: Kopp, P Arseven, OK Sabacan, L Kotlar, T Dupuis, J Cavaliere, H Santos, CLS Jameson, JL Medeiros-Neto, G
Citation: P. Kopp et al., Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene, J CLIN END, 84(1), 1999, pp. 336-341
Congenital and iodine - Deficiency goiters
Authors: Medeiros-Neto, G
Citation: G. Medeiros-neto, Congenital and iodine - Deficiency goiters, ATLAS OF CLINICAL ENDOCRINOLOGY, VOL 1, 1999, pp. 33
Risultati: 1-18 |