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Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency (2003)
Merjo, Livia M.; Elias, Lucila Leico Kagohara; Amaral, Fernando C.; Moreira, Ayrton Custódio; Castro, Margaret de
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FMRP
Assunto: ENDOCRINOLOGIA
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ABNT
MERJO, Livia M. et al. Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency. 2003, Anais.. Philadelphia: Endocrine Society, 2003. . Acesso em: 06 nov. 2025.
APA
Merjo, L. M., Elias, L. L. K., Amaral, F. C., Moreira, A. C., & Castro, M. de. (2003). Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency. In Program and Abstracts. Philadelphia: Endocrine Society.
NLM
Merjo LM, Elias LLK, Amaral FC, Moreira AC, Castro M de. Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency. Program and Abstracts. 2003 ;[citado 2025 nov. 06 ]
Vancouver
Merjo LM, Elias LLK, Amaral FC, Moreira AC, Castro M de. Molecular analysis of the hot spot area of the HSD3B2 gene in patientswith 3'beta'HSD deficiency. Program and Abstracts. 2003 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus (2002)
Elias, P. C. L.; Elias, Lucila L. L. K.; Torres, Natalia; Moreira, Ayrton Custódio; Antunes-Rodrigues, José; Castro, Margaret de
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FMRP
Assunto: ENDOCRINOLOGIA
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ABNT
ELIAS, P. C. L. et al. A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus. 2002, Anais.. San Francisco: Endocrine Society, 2002. . Acesso em: 06 nov. 2025.
APA
Elias, P. C. L., Elias, L. L. L. K., Torres, N., Moreira, A. C., Antunes-Rodrigues, J., & Castro, M. de. (2002). A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus. In Program and Abstracts. San Francisco: Endocrine Society.
NLM
Elias PCL, Elias LLLK, Torres N, Moreira AC, Antunes-Rodrigues J, Castro M de. A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus. Program and Abstracts. 2002 ;[citado 2025 nov. 06 ]
Vancouver
Elias PCL, Elias LLLK, Torres N, Moreira AC, Antunes-Rodrigues J, Castro M de. A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus. Program and Abstracts. 2002 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency (2002)
Castro, Margaret de; Penachioni, Junia Y.; Bachega, Tania A. S. S.; Mendonça, Berenice Bilharinho de; Fernandes, Vania F. T.; Kater, Claudio E.; Longui, Carlos A.; Moreira, Ayrton Custódio; Mello, Maricilda P.
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidades: FMRP, FM
Assunto: ENDOCRINOLOGIA
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ABNT
CASTRO, Margaret de et al. Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency. 2002, Anais.. San Francisco: Endocrine Society, 2002. . Acesso em: 06 nov. 2025.
APA
Castro, M. de, Penachioni, J. Y., Bachega, T. A. S. S., Mendonça, B. B. de, Fernandes, V. F. T., Kater, C. E., et al. (2002). Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency. In Program and Abstracts. San Francisco: Endocrine Society.
NLM
Castro M de, Penachioni JY, Bachega TASS, Mendonça BB de, Fernandes VFT, Kater CE, Longui CA, Moreira AC, Mello MP. Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency. Program and Abstracts. 2002 ;[citado 2025 nov. 06 ]
Vancouver
Castro M de, Penachioni JY, Bachega TASS, Mendonça BB de, Fernandes VFT, Kater CE, Longui CA, Moreira AC, Mello MP. Mutations in the CYP11B1 gene in Brazillian patients with 11'beta'-hidroxylase deficiency. Program and Abstracts. 2002 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Molecular screening and immunocytochemistry for RET proto-oncogene: role in the diagnosis and management of inherited Medullary Thyroid Carcinoma (2002)
Magalhães, P. K. R.; Castro, Margaret de; Elias, Lucila L. L. K.; Santos, Sandra S. R.; Torres, Natalia; Soares, Edson Garcia; Maciel, Léa Maria Zanini
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FMRP
Assunto: ENDOCRINOLOGIA
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ABNT
MAGALHÃES, P. K. R. et al. Molecular screening and immunocytochemistry for RET proto-oncogene: role in the diagnosis and management of inherited Medullary Thyroid Carcinoma. 2002, Anais.. San Francisco: Endocrine Society, 2002. . Acesso em: 06 nov. 2025.
APA
Magalhães, P. K. R., Castro, M. de, Elias, L. L. L. K., Santos, S. S. R., Torres, N., Soares, E. G., & Maciel, L. M. Z. (2002). Molecular screening and immunocytochemistry for RET proto-oncogene: role in the diagnosis and management of inherited Medullary Thyroid Carcinoma. In Program and Abstracts. San Francisco: Endocrine Society.
NLM
Magalhães PKR, Castro M de, Elias LLLK, Santos SSR, Torres N, Soares EG, Maciel LMZ. Molecular screening and immunocytochemistry for RET proto-oncogene: role in the diagnosis and management of inherited Medullary Thyroid Carcinoma. Program and Abstracts. 2002 ;[citado 2025 nov. 06 ]
Vancouver
Magalhães PKR, Castro M de, Elias LLLK, Santos SSR, Torres N, Soares EG, Maciel LMZ. Molecular screening and immunocytochemistry for RET proto-oncogene: role in the diagnosis and management of inherited Medullary Thyroid Carcinoma. Program and Abstracts. 2002 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Myocardial ultrasonic tissue characterization in patients with thyroid dysfunction (2002)
Almeida-Filho, Oswaldo C.; Maciel, Léa Maria Zanini; Pazin-Filho, Antonio; Schmidt, André; Maciel, Benedito Carlos
Source: Program and Abstracts. Conference titles: Annual Meeting of The Endocrine Society. Unidade: FMRP
Subjects: DOENÇAS DA TIREOIDE, ULTRASSONOGRAFIA (DIAGNÓSTICO), MIOCÁRDIO
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ABNT
ALMEIDA-FILHO, Oswaldo C. et al. Myocardial ultrasonic tissue characterization in patients with thyroid dysfunction. 2002, Anais.. San Francisco: Endocrine Society, 2002. . Acesso em: 06 nov. 2025.
APA
Almeida-Filho, O. C., Maciel, L. M. Z., Pazin-Filho, A., Schmidt, A., & Maciel, B. C. (2002). Myocardial ultrasonic tissue characterization in patients with thyroid dysfunction. In Program and Abstracts. San Francisco: Endocrine Society.
NLM
Almeida-Filho OC, Maciel LMZ, Pazin-Filho A, Schmidt A, Maciel BC. Myocardial ultrasonic tissue characterization in patients with thyroid dysfunction. Program and Abstracts. 2002 ;[citado 2025 nov. 06 ]
Vancouver
Almeida-Filho OC, Maciel LMZ, Pazin-Filho A, Schmidt A, Maciel BC. Myocardial ultrasonic tissue characterization in patients with thyroid dysfunction. Program and Abstracts. 2002 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Vitamin d3 growth inhibition of normal mammary cells: relationship to c-myc mrna expression (1996)
Escaleira, M T F; Brentani, Maria Mitzi
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Assunto: MEDICINA
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ABNT
ESCALEIRA, M T F e BRENTANI, Maria Mitzi. Vitamin d3 growth inhibition of normal mammary cells: relationship to c-myc mrna expression. 1996, Anais.. San Francisco: Endocrine Society, 1996. . Acesso em: 06 nov. 2025.
APA
Escaleira, M. T. F., & Brentani, M. M. (1996). Vitamin d3 growth inhibition of normal mammary cells: relationship to c-myc mrna expression. In Program and Abstracts. San Francisco: Endocrine Society.
NLM
Escaleira MTF, Brentani MM. Vitamin d3 growth inhibition of normal mammary cells: relationship to c-myc mrna expression. Program and Abstracts. 1996 ;[citado 2025 nov. 06 ]
Vancouver
Escaleira MTF, Brentani MM. Vitamin d3 growth inhibition of normal mammary cells: relationship to c-myc mrna expression. Program and Abstracts. 1996 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Missense mutation in the lh receptor gene causas leydig cell hypoplasia (1995)
Themmen, A P N; Kraais, R; Kremer, H; Post, M; Toledo, S. P. A.; Brunner, H G; Grootegoed, J A
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
THEMMEN, A P N et al. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 06 nov. 2025.
APA
Themmen, A. P. N., Kraais, R., Kremer, H., Post, M., Toledo, S. P. A., Brunner, H. G., & Grootegoed, J. A. (1995). Missense mutation in the lh receptor gene causas leydig cell hypoplasia. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Vancouver
Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Metformin treatment changes insulin receptor bindig and tyrosine kinase activity of obese subjects with normal glucose tolerance (1995)
Santos, R F; Nomizo, R; Rosco, A; Wajchenberg, B L
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
SANTOS, R F et al. Metformin treatment changes insulin receptor bindig and tyrosine kinase activity of obese subjects with normal glucose tolerance. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 06 nov. 2025.
APA
Santos, R. F., Nomizo, R., Rosco, A., & Wajchenberg, B. L. (1995). Metformin treatment changes insulin receptor bindig and tyrosine kinase activity of obese subjects with normal glucose tolerance. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Santos RF, Nomizo R, Rosco A, Wajchenberg BL. Metformin treatment changes insulin receptor bindig and tyrosine kinase activity of obese subjects with normal glucose tolerance. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Vancouver
Santos RF, Nomizo R, Rosco A, Wajchenberg BL. Metformin treatment changes insulin receptor bindig and tyrosine kinase activity of obese subjects with normal glucose tolerance. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Basal and pulsatile gh 24 hours secretion in active and cured acromegaly and normal subjects (1995)
Semer, M; Salgado, L R; Knoepfelmacher, M; Nery, M; Wajchenberg, B L; Liberman, Bernardo
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
SEMER, M et al. Basal and pulsatile gh 24 hours secretion in active and cured acromegaly and normal subjects. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 06 nov. 2025.
APA
Semer, M., Salgado, L. R., Knoepfelmacher, M., Nery, M., Wajchenberg, B. L., & Liberman, B. (1995). Basal and pulsatile gh 24 hours secretion in active and cured acromegaly and normal subjects. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Semer M, Salgado LR, Knoepfelmacher M, Nery M, Wajchenberg BL, Liberman B. Basal and pulsatile gh 24 hours secretion in active and cured acromegaly and normal subjects. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Vancouver
Semer M, Salgado LR, Knoepfelmacher M, Nery M, Wajchenberg BL, Liberman B. Basal and pulsatile gh 24 hours secretion in active and cured acromegaly and normal subjects. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Circardian variation of plasma atrial natriuretic peptid (anp) corticostere and acth in rats (1995)
Oliveira, M H A; Moreira, Ayrton Custódio; Antunes-Rodrigues, José
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FMRP
Assunto: ENDODONTIA
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ABNT
OLIVEIRA, M H A e MOREIRA, Ayrton Custódio e ANTUNES-RODRIGUES, José. Circardian variation of plasma atrial natriuretic peptid (anp) corticostere and acth in rats. 1995, Anais.. Washington: Endocrine Society, 1995. . Acesso em: 06 nov. 2025.
APA
Oliveira, M. H. A., Moreira, A. C., & Antunes-Rodrigues, J. (1995). Circardian variation of plasma atrial natriuretic peptid (anp) corticostere and acth in rats. In Program and Abstracts. Washington: Endocrine Society.
NLM
Oliveira MHA, Moreira AC, Antunes-Rodrigues J. Circardian variation of plasma atrial natriuretic peptid (anp) corticostere and acth in rats. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Vancouver
Oliveira MHA, Moreira AC, Antunes-Rodrigues J. Circardian variation of plasma atrial natriuretic peptid (anp) corticostere and acth in rats. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients (1995)
Borges, M F; Abelin, N M A; Barros, M A E; Resende, E A M; Toledo, S. P. A.
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
BORGES, M F et al. Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients. 1995, Anais.. Washington: Endocrine Society, 1995. . Acesso em: 06 nov. 2025.
APA
Borges, M. F., Abelin, N. M. A., Barros, M. A. E., Resende, E. A. M., & Toledo, S. P. A. (1995). Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients. In Program and Abstracts. Washington: Endocrine Society.
NLM
Borges MF, Abelin NMA, Barros MAE, Resende EAM, Toledo SPA. Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Vancouver
Borges MF, Abelin NMA, Barros MAE, Resende EAM, Toledo SPA. Calcitonin (ct) levels during combined stimulation test with calcium ('CA POT.2+') and pentagastrin (pg) by ria and irma methods in normal subjects and in thyroidectomized patients. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Resistance to adh action on the kidney in patients with cushing's disease (1995)
Knoepfelmacher, M; Pradal, M J; Di Dio, R; Salgado, L R; Semer, M; Wajchenberg, B L; Liberman, Bernardo
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
KNOEPFELMACHER, M et al. Resistance to adh action on the kidney in patients with cushing's disease. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 06 nov. 2025.
APA
Knoepfelmacher, M., Pradal, M. J., Di Dio, R., Salgado, L. R., Semer, M., Wajchenberg, B. L., & Liberman, B. (1995). Resistance to adh action on the kidney in patients with cushing's disease. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Knoepfelmacher M, Pradal MJ, Di Dio R, Salgado LR, Semer M, Wajchenberg BL, Liberman B. Resistance to adh action on the kidney in patients with cushing's disease. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Vancouver
Knoepfelmacher M, Pradal MJ, Di Dio R, Salgado LR, Semer M, Wajchenberg BL, Liberman B. Resistance to adh action on the kidney in patients with cushing's disease. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Molecular analysis of p53 vhl and ret genes in pheochromocytoma (1995)
Dahia, P L M; Aguiar, R C T; Eng, C; Crossey, P A; Maher, E R; Grossman, A; Ponder, B A J; Toledo, S. P. A.
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
DAHIA, P L M et al. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 06 nov. 2025.
APA
Dahia, P. L. M., Aguiar, R. C. T., Eng, C., Crossey, P. A., Maher, E. R., Grossman, A., et al. (1995). Molecular analysis of p53 vhl and ret genes in pheochromocytoma. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Dahia PLM, Aguiar RCT, Eng C, Crossey PA, Maher ER, Grossman A, Ponder BAJ, Toledo SPA. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Vancouver
Dahia PLM, Aguiar RCT, Eng C, Crossey PA, Maher ER, Grossman A, Ponder BAJ, Toledo SPA. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency (1995)
Mendonça, B. B.; Arnhold, I J P; Pelegrinelli, A C; Frade, E C; Latronico, A C; Lin, C J; Marcondes, J A M; Nicolau, Wilian; Bloise, W; Wajchenberg, B L
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
MENDONÇA, B. B. et al. Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 06 nov. 2025.
APA
Mendonça, B. B., Arnhold, I. J. P., Pelegrinelli, A. C., Frade, E. C., Latronico, A. C., Lin, C. J., et al. (1995). Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency. In Program and Abstracts. Rockville: Endocrine Society.
NLM
Mendonça BB, Arnhold IJP, Pelegrinelli AC, Frade EC, Latronico AC, Lin CJ, Marcondes JAM, Nicolau W, Bloise W, Wajchenberg BL. Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Vancouver
Mendonça BB, Arnhold IJP, Pelegrinelli AC, Frade EC, Latronico AC, Lin CJ, Marcondes JAM, Nicolau W, Bloise W, Wajchenberg BL. Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency. Program and Abstracts. 1995 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Peak detection analysis of 12-hour secretion of gonadotropins in normals and women with clinical hyperandrogenism (1994)
Minanni, S L; Cavaleiro, A M S; Fortes, M A H Z; Rego, M A; Marcondes, J A M; Mendonça, B. B.; Vezozzo, D C P; Wajchenberg, B L; Rodbard, D; Giannella Neto, D
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
MINANNI, S L et al. Peak detection analysis of 12-hour secretion of gonadotropins in normals and women with clinical hyperandrogenism. 1994, Anais.. Anaheim: Endocrine Society, 1994. . Acesso em: 06 nov. 2025.
APA
Minanni, S. L., Cavaleiro, A. M. S., Fortes, M. A. H. Z., Rego, M. A., Marcondes, J. A. M., Mendonça, B. B., et al. (1994). Peak detection analysis of 12-hour secretion of gonadotropins in normals and women with clinical hyperandrogenism. In Program and Abstracts. Anaheim: Endocrine Society.
NLM
Minanni SL, Cavaleiro AMS, Fortes MAHZ, Rego MA, Marcondes JAM, Mendonça BB, Vezozzo DCP, Wajchenberg BL, Rodbard D, Giannella Neto D. Peak detection analysis of 12-hour secretion of gonadotropins in normals and women with clinical hyperandrogenism. Program and Abstracts. 1994 ;[citado 2025 nov. 06 ]
Vancouver
Minanni SL, Cavaleiro AMS, Fortes MAHZ, Rego MA, Marcondes JAM, Mendonça BB, Vezozzo DCP, Wajchenberg BL, Rodbard D, Giannella Neto D. Peak detection analysis of 12-hour secretion of gonadotropins in normals and women with clinical hyperandrogenism. Program and Abstracts. 1994 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Effect of pdgf isoforms on dna synthesis , igf-i gene expression, and 24 kd igfbp secretion by human aortic smooth muscle cell (smc) in culture (1994)
Correa, M L C; Oliveira, M. R.; Pares, M M N S; Bydlowski, Sérgio Paulo; Chamone, Dalton de Alencar Fischer; Wajchenberg, B L; Gianella Neto, D
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: HEMATOLOGIA
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ABNT
CORREA, M L C et al. Effect of pdgf isoforms on dna synthesis , igf-i gene expression, and 24 kd igfbp secretion by human aortic smooth muscle cell (smc) in culture. 1994, Anais.. Anaheim: Endocrine Society, 1994. . Acesso em: 06 nov. 2025.
APA
Correa, M. L. C., Oliveira, M. R., Pares, M. M. N. S., Bydlowski, S. P., Chamone, D. de A. F., Wajchenberg, B. L., & Gianella Neto, D. (1994). Effect of pdgf isoforms on dna synthesis , igf-i gene expression, and 24 kd igfbp secretion by human aortic smooth muscle cell (smc) in culture. In Program and Abstracts. Anaheim: Endocrine Society.
NLM
Correa MLC, Oliveira MR, Pares MMNS, Bydlowski SP, Chamone D de AF, Wajchenberg BL, Gianella Neto D. Effect of pdgf isoforms on dna synthesis , igf-i gene expression, and 24 kd igfbp secretion by human aortic smooth muscle cell (smc) in culture. Program and Abstracts. 1994 ;[citado 2025 nov. 06 ]
Vancouver
Correa MLC, Oliveira MR, Pares MMNS, Bydlowski SP, Chamone D de AF, Wajchenberg BL, Gianella Neto D. Effect of pdgf isoforms on dna synthesis , igf-i gene expression, and 24 kd igfbp secretion by human aortic smooth muscle cell (smc) in culture. Program and Abstracts. 1994 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing (1992)
Toledo, S. P. A.; Oliveira Filho, R. M.; Moreira-Filho, Carlos Alberto; Charreau, E H
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidades: ICB, FM
Assunto: IMUNOLOGIA
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ABNT
TOLEDO, S. P. A. et al. Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing. 1992, Anais.. Bethesda: Endocrine Society, 1992. . Acesso em: 06 nov. 2025.
APA
Toledo, S. P. A., Oliveira Filho, R. M., Moreira-Filho, C. A., & Charreau, E. H. (1992). Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing. In Program and Abstracts. Bethesda: Endocrine Society.
NLM
Toledo SPA, Oliveira Filho RM, Moreira-Filho CA, Charreau EH. Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing. Program and Abstracts. 1992 ;[citado 2025 nov. 06 ]
Vancouver
Toledo SPA, Oliveira Filho RM, Moreira-Filho CA, Charreau EH. Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing. Program and Abstracts. 1992 ;[citado 2025 nov. 06 ]
Trabalho de evento-resumo
Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin (1991)
Targovnik, H M; Varela, V; Abatangelo, C; Wajchenberg, B L; Medeiros Neto, Geraldo Antônio
Source: Program and Abstracts. Conference titles: Annual Meeting of the Endocrine Society. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TARGOVNIK, H M et al. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. 1991, Anais.. Washington: Endocrine Society, 1991. . Acesso em: 06 nov. 2025.
APA
Targovnik, H. M., Varela, V., Abatangelo, C., Wajchenberg, B. L., & Medeiros Neto, G. A. (1991). Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. In Program and Abstracts. Washington: Endocrine Society.
NLM
Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. Program and Abstracts. 1991 ;[citado 2025 nov. 06 ]
Vancouver
Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. Program and Abstracts. 1991 ;[citado 2025 nov. 06 ]

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