Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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11 |
Material Type: Artigo
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Phenocopies for Deafness and Goiter Development in a Large Inbred Brazilian Kindred with Pendred’s Syndrome Associated with a Novel Mutation in the PDS Gene1Kopp, P ; Arseven, O. Karamanoglu ; Sabacan, L ; Kotlar, T ; Dupuis, J ; Cavaliere, H ; Santos, C. L. S ; Jameson, J. L ; Medeiros-Neto, GThe journal of clinical endocrinology and metabolism, 1999-01, Vol.84 (1), p.336-341 [Periódico revisado por pares]Endocrine SocietyTexto completo disponível |
12 |
Material Type: Artigo
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Thyrotropin Receptor Mutations in Hyperfunctioning Thyroid Adenomas from BrazilNogueira, C R ; Kopp, P ; Arseven, O K ; Santos, C L ; Jameson, J L ; Medeiros-Neto, GThyroid (New York, N.Y.), 1999-11, Vol.9 (11), p.163-1068 [Periódico revisado por pares]United StatesTexto completo disponível |
13 |
Material Type: Artigo
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Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidismNguyen, Lynda Q ; Arseven, Onur Karamanoglu ; Gerber, Hans ; Stein, Barbara S ; Jameson, J Larry ; Kopp, PeterEndocrinology (Philadelphia), 2002-02, Vol.143 (2), p.395-402 [Periódico revisado por pares]United StatesTexto completo disponível |
14 |
Material Type: Artigo
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Structural Analysis of the Thyrotropin Receptor in Four Patients with Congenital Hypothyroidism Due to Thyroid HypoplasiaNogueira, C R ; Nguyen, L Q ; Coelho-Neto, J R ; Arseven, O K ; Jameson, J L ; Kopp, P ; Medeiros-Neto, G AThyroid (New York, N.Y.), 1999-06, Vol.9 (6), p.523-529 [Periódico revisado por pares]United StatesTexto completo disponível |