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Results: 1-6 |
Results: 6

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

Authors: Arseven, OK Wilkes, WP Jameson, JL Kopp, P
Citation: Ok. Arseven et al., Substitutions of tyrosine 601 in the human thyrotropin receptor result in increase or loss of basal activation of the cyclic adenosine monophosphate pathway and disrupt coupling to G(q/11), THYROID, 10(1), 2000, pp. 3-10

Authors: Nogueira, CR Nguyen, LQ Coelho-Neto, JR Arseven, OK Jameson, JL Kopp, P Medeiros-Neto, GA
Citation: Cr. Nogueira et al., Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia, THYROID, 9(6), 1999, pp. 523-529

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

Authors: Nogueira, CR Nguyen, LQ Coelho-Neto, JR Arseven, OK Jameson, JL Kopp, P Medeiros-Neto, GA
Citation: Cr. Nogueira et al., Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia (vol 9, pg 523, 1999), THYROID, 9(11), 1999, pp. 1159-1159

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
Risultati: 1-6 |