ReP USP - Resultado da busca

Trabalho de evento-resumo periodico
Genotype-phenotype correlation in brazilian patients with congenital goiter and hypothyroidism due to thyroglobulin gene mutations (2008)
Pardo, V.; Knobel, I.; Toniolo, J.; Oliveira, M.; Kopp, P.; Medeiros Neto, Geraldo Antônio
Fonte: Thyroid. Nome do evento: Annual Meeting of the American Thyroid Association. Unidade: FM
Assuntos: HIPOTIREOIDISMO, MUTAÇÃO GENÉTICA, BRASILEIROS
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ABNT
PARDO, V. et al. Genotype-phenotype correlation in brazilian patients with congenital goiter and hypothyroidism due to thyroglobulin gene mutations. Thyroid. Chicago: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 02 nov. 2025. , 2008
APA
Pardo, V., Knobel, I., Toniolo, J., Oliveira, M., Kopp, P., & Medeiros Neto, G. A. (2008). Genotype-phenotype correlation in brazilian patients with congenital goiter and hypothyroidism due to thyroglobulin gene mutations. Thyroid. Chicago: Faculdade de Medicina, Universidade de São Paulo.
NLM
Pardo V, Knobel I, Toniolo J, Oliveira M, Kopp P, Medeiros Neto GA. Genotype-phenotype correlation in brazilian patients with congenital goiter and hypothyroidism due to thyroglobulin gene mutations. Thyroid. 2008 ; 18[citado 2025 nov. 02 ]
Vancouver
Pardo V, Knobel I, Toniolo J, Oliveira M, Kopp P, Medeiros Neto GA. Genotype-phenotype correlation in brazilian patients with congenital goiter and hypothyroidism due to thyroglobulin gene mutations. Thyroid. 2008 ; 18[citado 2025 nov. 02 ]
Trabalho de evento
Three brazilian families with congenital goiter and defective thyroglobolin synthesis associated with a novel homozygous mutation (A2234N) in the thyroglobulin gene (2002)
Vono-Toniolo, J.; Medeiros Neto, Geraldo Antônio; Kopp, P.
Nome do evento: Annual Meeting of the American Thyroid Association. Unidade: FM
Assuntos: HIPOTIROIDISMO (GENÉTICA), RADIOIMUNOENSAIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VONO-TONIOLO, J. e MEDEIROS NETO, Geraldo Antônio e KOPP, P. Three brazilian families with congenital goiter and defective thyroglobolin synthesis associated with a novel homozygous mutation (A2234N) in the thyroglobulin gene. 2002, Anais.. Los Angeles, CA: Faculdade de Medicina, Universidade de São Paulo, 2002. . Acesso em: 02 nov. 2025.
APA
Vono-Toniolo, J., Medeiros Neto, G. A., & Kopp, P. (2002). Three brazilian families with congenital goiter and defective thyroglobolin synthesis associated with a novel homozygous mutation (A2234N) in the thyroglobulin gene. In . Los Angeles, CA: Faculdade de Medicina, Universidade de São Paulo.
NLM
Vono-Toniolo J, Medeiros Neto GA, Kopp P. Three brazilian families with congenital goiter and defective thyroglobolin synthesis associated with a novel homozygous mutation (A2234N) in the thyroglobulin gene. 2002 ;[citado 2025 nov. 02 ]
Vancouver
Vono-Toniolo J, Medeiros Neto GA, Kopp P. Three brazilian families with congenital goiter and defective thyroglobolin synthesis associated with a novel homozygous mutation (A2234N) in the thyroglobulin gene. 2002 ;[citado 2025 nov. 02 ]
Trabalho de evento-anais periodico
Clinical and molecular analysis of three Mexican families with Pendred's syndrome (2001)
Trevino, O. Gonzalez; Arseven Karamanoglu, O.; Ceballos, C. J.; Vives, V. I.; Ramirez, R. C.; Gomez, V. V.; Medeiros-Neto, G.; Kopp, P.
Fonte: European Journal of Endocrinology. Unidade: FM
Assuntos: CLÍNICA GERAL, ENDOCRINOLOGIA
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ABNT
TREVINO, O. Gonzalez et al. Clinical and molecular analysis of three Mexican families with Pendred's syndrome. European Journal of Endocrinology. Reino Unido: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 02 nov. 2025. , 2001
APA
Trevino, O. G., Arseven Karamanoglu, O., Ceballos, C. J., Vives, V. I., Ramirez, R. C., Gomez, V. V., et al. (2001). Clinical and molecular analysis of three Mexican families with Pendred's syndrome. European Journal of Endocrinology. Reino Unido: Faculdade de Medicina, Universidade de São Paulo.
NLM
Trevino OG, Arseven Karamanoglu O, Ceballos CJ, Vives VI, Ramirez RC, Gomez VV, Medeiros-Neto G, Kopp P. Clinical and molecular analysis of three Mexican families with Pendred's syndrome. European Journal of Endocrinology. 2001 ; 144( 6): 585-593.[citado 2025 nov. 02 ]
Vancouver
Trevino OG, Arseven Karamanoglu O, Ceballos CJ, Vives VI, Ramirez RC, Gomez VV, Medeiros-Neto G, Kopp P. Clinical and molecular analysis of three Mexican families with Pendred's syndrome. European Journal of Endocrinology. 2001 ; 144( 6): 585-593.[citado 2025 nov. 02 ]
Artigo de periodico
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 (1999)
Kopp, P.; Arseven, O. Karamanoglu; Sabacan, L.; Kotlar, T.; Dupuis, J.; Cavalieri, H.; Santos, C. L. S.; Jameson, J. L.; Medeiros Neto, Geraldo Antônio
Fonte: Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Assuntos: ENDOCRINOPATIAS, ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOPP, P. 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. Journal of Clinical Endocrinology & Metabolism, v. 84, n. 1, p. 336-341, 1999Tradução . . Acesso em: 02 nov. 2025.
APA
Kopp, P., Arseven, O. K., Sabacan, L., Kotlar, T., Dupuis, J., Cavalieri, H., et al. (1999). 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. Journal of Clinical Endocrinology & Metabolism, 84( 1), 336-341.
NLM
Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavalieri H, Santos CLS, Jameson JL, Medeiros Neto GA. 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. Journal of Clinical Endocrinology & Metabolism. 1999 ; 84( 1): 336-341.[citado 2025 nov. 02 ]
Vancouver
Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavalieri H, Santos CLS, Jameson JL, Medeiros Neto GA. 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. Journal of Clinical Endocrinology & Metabolism. 1999 ; 84( 1): 336-341.[citado 2025 nov. 02 ]
Artigo de periodico
Molecular analysis of the TSH-receptor gene in five kindreds with congenital hypothyroidism due to thyroid hypoplasia (1998)
Nogueira, C. R.; Kopp, P.; Rodrigues, J.; Medeiros-Neto, G.
Fonte: The thyroid and age. Nome do evento: Merck European Thyroid Symposium. Unidade: FM
Assunto: HIPERTIREOIDISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NOGUEIRA, C. R. et al. Molecular analysis of the TSH-receptor gene in five kindreds with congenital hypothyroidism due to thyroid hypoplasia. The thyroid and age, p. 2, 1998Tradução . . Acesso em: 02 nov. 2025.
APA
Nogueira, C. R., Kopp, P., Rodrigues, J., & Medeiros-Neto, G. (1998). Molecular analysis of the TSH-receptor gene in five kindreds with congenital hypothyroidism due to thyroid hypoplasia. The thyroid and age, 2.
NLM
Nogueira CR, Kopp P, Rodrigues J, Medeiros-Neto G. Molecular analysis of the TSH-receptor gene in five kindreds with congenital hypothyroidism due to thyroid hypoplasia. The thyroid and age. 1998 ; 2.[citado 2025 nov. 02 ]
Vancouver
Nogueira CR, Kopp P, Rodrigues J, Medeiros-Neto G. Molecular analysis of the TSH-receptor gene in five kindreds with congenital hypothyroidism due to thyroid hypoplasia. The thyroid and age. 1998 ; 2.[citado 2025 nov. 02 ]

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