ReP USP - Resultado da busca

Artigo de periodico
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole (2008)
Almeida, Madson Queiroz; Brito, Vinicius Nahime; Lins, Thereza Selma S.; Guerra-Júnior, Gil; Castro, Margaret de; Antonini, Sonir Roberto; Arnhold, Ivo Jorge Prado; Mendonça, Berenice Bilharinho; Latronico, Ana Claudia
Source: Clinical Endocrinology. Unidades: FM, FMRP
Subjects: ENDOCRINOLOGIA, PUBERDADE PRECOCE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA, Madson Queiroz et al. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole. Clinical Endocrinology, v. 69, n. 1, p. 93-98, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2007.03160.x. Acesso em: 28 set. 2024.
APA
Almeida, M. Q., Brito, V. N., Lins, T. S. S., Guerra-Júnior, G., Castro, M. de, Antonini, S. R., et al. (2008). Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole. Clinical Endocrinology, 69( 1), 93-98. doi:10.1111/j.1365-2265.2007.03160.x
NLM
Almeida MQ, Brito VN, Lins TSS, Guerra-Júnior G, Castro M de, Antonini SR, Arnhold IJP, Mendonça BB, Latronico AC. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole [Internet]. Clinical Endocrinology. 2008 ; 69( 1): 93-98.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03160.x
Vancouver
Almeida MQ, Brito VN, Lins TSS, Guerra-Júnior G, Castro M de, Antonini SR, Arnhold IJP, Mendonça BB, Latronico AC. Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole [Internet]. Clinical Endocrinology. 2008 ; 69( 1): 93-98.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1365-2265.2007.03160.x
Artigo de periodico
Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion (2006)
Abrão, Milena Garcia; Leitet, M. V.; Carvalho, L. R.; Billerbeck, A. E. C.; Nishi, M. Y.; Barbosa, A. S.; Martin, R. M.; Arnhold, I. J. P.; Mendonça, Berenice Bilharinho
Source: Clinical Endocrinology. Unidade: FM
Subjects: ENDOCRINOLOGIA, HORMÔNIOS HIPOFISÁRIOS (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABRÃO, Milena Garcia et al. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion. Clinical Endocrinology, v. 65, n. 3, p. 294-300, 2006Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2006.02592.x. Acesso em: 28 set. 2024.
APA
Abrão, M. G., Leitet, M. V., Carvalho, L. R., Billerbeck, A. E. C., Nishi, M. Y., Barbosa, A. S., et al. (2006). Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion. Clinical Endocrinology, 65( 3), 294-300. doi:10.1111/j.1365-2265.2006.02592.x
NLM
Abrão MG, Leitet MV, Carvalho LR, Billerbeck AEC, Nishi MY, Barbosa AS, Martin RM, Arnhold IJP, Mendonça BB. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion [Internet]. Clinical Endocrinology. 2006 ; 65( 3): 294-300.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02592.x
Vancouver
Abrão MG, Leitet MV, Carvalho LR, Billerbeck AEC, Nishi MY, Barbosa AS, Martin RM, Arnhold IJP, Mendonça BB. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion [Internet]. Clinical Endocrinology. 2006 ; 65( 3): 294-300.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1365-2265.2006.02592.x
Artigo de periodico
The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH anlogue therapy not restored by dihydrotestosterone administration (2004)
Jorge, Alexander A. L.; Souza, Silvia C. A. L.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
JORGE, Alexander A. L. et al. The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH anlogue therapy not restored by dihydrotestosterone administration. Clinical Endocrinology, v. 60, p. 36-40, 2004Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2004.01930.x. Acesso em: 28 set. 2024.
APA
Jorge, A. A. L., Souza, S. C. A. L., Arnhold, I. J. P., & Mendonça, B. B. (2004). The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH anlogue therapy not restored by dihydrotestosterone administration. Clinical Endocrinology, 60, 36-40. doi:10.1111/j.1365-2265.2004.01930.x
NLM
Jorge AAL, Souza SCAL, Arnhold IJP, Mendonça BB. The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH anlogue therapy not restored by dihydrotestosterone administration [Internet]. Clinical Endocrinology. 2004 ; 60 36-40.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1365-2265.2004.01930.x
Vancouver
Jorge AAL, Souza SCAL, Arnhold IJP, Mendonça BB. The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH anlogue therapy not restored by dihydrotestosterone administration [Internet]. Clinical Endocrinology. 2004 ; 60 36-40.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1365-2265.2004.01930.x
Artigo de periodico
Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy (2003)
Carvalho, Luciani R.; Faria, Maria Estela Justamante de; Osorio, Maria Geralda Farah; Estefan, Vivian; Jorge, Alexander Augusto Lima; Arnhold, Ivo Jorge P.; Mendonça, Berenice B.
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Luciani R. et al. Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy. Clinical Endocrinology, v. 59, p. 788-792, 2003Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2003.01899.x. Acesso em: 28 set. 2024.
APA
Carvalho, L. R., Faria, M. E. J. de, Osorio, M. G. F., Estefan, V., Jorge, A. A. L., Arnhold, I. J. P., & Mendonça, B. B. (2003). Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy. Clinical Endocrinology, 59, 788-792. doi:10.1046/j.1365-2265.2003.01899.x
NLM
Carvalho LR, Faria MEJ de, Osorio MGF, Estefan V, Jorge AAL, Arnhold IJP, Mendonça BB. Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy [Internet]. Clinical Endocrinology. 2003 ; 59 788-792.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01899.x
Vancouver
Carvalho LR, Faria MEJ de, Osorio MGF, Estefan V, Jorge AAL, Arnhold IJP, Mendonça BB. Acromegalic features in growth hormore (GH)-deficient patients after long-term GH therapy [Internet]. Clinical Endocrinology. 2003 ; 59 788-792.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01899.x
Artigo de periodico
Glucocorticoid receptor gene polymorphism in ACTH-secreting pituitary tumours (2002)
Antonini, S. R. R.; Latronico, Ana Claudia; Elias, L. L. K.; Cukier, A.; Machado, H. R.; Liberman, Bernardo; Mendonça, Berenice B.; Moreira, Ayrton Custódio; Castro, M.
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANTONINI, S. R. R. et al. Glucocorticoid receptor gene polymorphism in ACTH-secreting pituitary tumours. Clinical Endocrinology, v. 57, n. 05, p. 657-662, 2002Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2002.01639.x. Acesso em: 28 set. 2024.
APA
Antonini, S. R. R., Latronico, A. C., Elias, L. L. K., Cukier, A., Machado, H. R., Liberman, B., et al. (2002). Glucocorticoid receptor gene polymorphism in ACTH-secreting pituitary tumours. Clinical Endocrinology, 57( 05), 657-662. doi:10.1046/j.1365-2265.2002.01639.x
NLM
Antonini SRR, Latronico AC, Elias LLK, Cukier A, Machado HR, Liberman B, Mendonça BB, Moreira AC, Castro M. Glucocorticoid receptor gene polymorphism in ACTH-secreting pituitary tumours [Internet]. Clinical Endocrinology. 2002 ; 57( 05): 657-662.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.2002.01639.x
Vancouver
Antonini SRR, Latronico AC, Elias LLK, Cukier A, Machado HR, Liberman B, Mendonça BB, Moreira AC, Castro M. Glucocorticoid receptor gene polymorphism in ACTH-secreting pituitary tumours [Internet]. Clinical Endocrinology. 2002 ; 57( 05): 657-662.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.2002.01639.x
Artigo de periodico
Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors (2002)
Antonini, S. R. R.; Latronicot, A. C.; ELIAS, L. L. K.; Cukiert, A. (Hospital Brigadeiro-US, São Paulo, Brasil); Machado, Hélio Rubens; Liberman, Bernardo; Mendonça, Berenice Bilharinho de; Moreira, Ayrton Custódio; Castro, Margaret de
Source: Clinical Endocrinology. Unidades: FMRP, FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANTONINI, S. R. R. et al. Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors. Clinical Endocrinology, v. 57, p. 657-662, 2002Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2002.01639.x. Acesso em: 28 set. 2024.
APA
Antonini, S. R. R., Latronicot, A. C., ELIAS, L. L. K., Machado, H. R., Liberman, B., Mendonça, B. B. de, et al. (2002). Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors. Clinical Endocrinology, 57, 657-662. doi:10.1046/j.1365-2265.2002.01639.x
NLM
Antonini SRR, Latronicot AC, ELIAS LLK, Machado HR, Liberman B, Mendonça BB de, Moreira AC, Castro M de. Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors [Internet]. Clinical Endocrinology. 2002 ; 57 657-662.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.2002.01639.x
Vancouver
Antonini SRR, Latronicot AC, ELIAS LLK, Machado HR, Liberman B, Mendonça BB de, Moreira AC, Castro M de. Glucocorticoid receptor gene polymorphysms in ACTH-secreting pituitary tumors [Internet]. Clinical Endocrinology. 2002 ; 57 657-662.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.2002.01639.x
Artigo de periodico
Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil (2000)
Barca, Maria Fernanda; Knobel, Meyer; Tomimori, Eduardo; Cardia, Maria Silvia; Medeiros Neto, Geraldo Antônio
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARCA, Maria Fernanda et al. Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil. Clinical Endocrinology, v. 53, p. 21-31, 2000Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2000.01034.x. Acesso em: 28 set. 2024.
APA
Barca, M. F., Knobel, M., Tomimori, E., Cardia, M. S., & Medeiros Neto, G. A. (2000). Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil. Clinical Endocrinology, 53, 21-31. doi:10.1046/j.1365-2265.2000.01034.x
NLM
Barca MF, Knobel M, Tomimori E, Cardia MS, Medeiros Neto GA. Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil [Internet]. Clinical Endocrinology. 2000 ; 53 21-31.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.2000.01034.x
Vancouver
Barca MF, Knobel M, Tomimori E, Cardia MS, Medeiros Neto GA. Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil [Internet]. Clinical Endocrinology. 2000 ; 53 21-31.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.2000.01034.x
Artigo de periodico
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect (1999)
Santos, Cecilia L. S.; Bikker, Hennie; Rego, Katia G. M.; Nascimento, Antonio C.; Tambascia, Marcos; Vijlder, Jan J. M. de; Medeiros Neto, Geraldo Antônio
Source: Clinical Endocrinology. Unidade: FM
Subjects: ENDOCRINOLOGIA, HORMÔNIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Cecilia L. S. et al. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect. Clinical Endocrinology, v. 51, n. 2, p. 165-172, 1999Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1999.00746.x. Acesso em: 28 set. 2024.
APA
Santos, C. L. S., Bikker, H., Rego, K. G. M., Nascimento, A. C., Tambascia, M., Vijlder, J. J. M. de, & Medeiros Neto, G. A. (1999). A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect. Clinical Endocrinology, 51( 2), 165-172. doi:10.1046/j.1365-2265.1999.00746.x
NLM
Santos CLS, Bikker H, Rego KGM, Nascimento AC, Tambascia M, Vijlder JJM de, Medeiros Neto GA. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect [Internet]. Clinical Endocrinology. 1999 ; 51( 2): 165-172.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00746.x
Vancouver
Santos CLS, Bikker H, Rego KGM, Nascimento AC, Tambascia M, Vijlder JJM de, Medeiros Neto GA. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect [Internet]. Clinical Endocrinology. 1999 ; 51( 2): 165-172.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00746.x
Artigo de periodico
Clinical features of women with resistance to luteinizing hormone (1999)
Arnhold, Ivo J. P.; Latrônico, Ana C.; Batista, Marcelo C.; Izzo, Carlos R.; Mendonça, Berenice Bilharinho de
Source: Clinical Endocrinology. Unidade: FM
Subjects: ENDOCRINOLOGIA, HORMÔNIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARNHOLD, Ivo J. P. et al. Clinical features of women with resistance to luteinizing hormone. Clinical Endocrinology, v. 51, n. 6, p. 701-707, 1999Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1999.00863.x. Acesso em: 28 set. 2024.
APA
Arnhold, I. J. P., Latrônico, A. C., Batista, M. C., Izzo, C. R., & Mendonça, B. B. de. (1999). Clinical features of women with resistance to luteinizing hormone. Clinical Endocrinology, 51( 6), 701-707. doi:10.1046/j.1365-2265.1999.00863.x
NLM
Arnhold IJP, Latrônico AC, Batista MC, Izzo CR, Mendonça BB de. Clinical features of women with resistance to luteinizing hormone [Internet]. Clinical Endocrinology. 1999 ; 51( 6): 701-707.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00863.x
Vancouver
Arnhold IJP, Latrônico AC, Batista MC, Izzo CR, Mendonça BB de. Clinical features of women with resistance to luteinizing hormone [Internet]. Clinical Endocrinology. 1999 ; 51( 6): 701-707.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00863.x
Artigo de periodico
Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas (1996)
Aguiar, Ricardo C T; Dahia, Patricia L M; Sill, Heinz; Toledo, S. P. A.; Goldman, John M; Cross, Nicholas C P
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AGUIAR, Ricardo C T et al. Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas. Clinical Endocrinology, v. 45, n. 1, p. 93-96, 1996Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1996.00762.x. Acesso em: 28 set. 2024.
APA
Aguiar, R. C. T., Dahia, P. L. M., Sill, H., Toledo, S. P. A., Goldman, J. M., & Cross, N. C. P. (1996). Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas. Clinical Endocrinology, 45( 1), 93-96. doi:10.1046/j.1365-2265.1996.00762.x
NLM
Aguiar RCT, Dahia PLM, Sill H, Toledo SPA, Goldman JM, Cross NCP. Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas [Internet]. Clinical Endocrinology. 1996 ; 45( 1): 93-96.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.1996.00762.x
Vancouver
Aguiar RCT, Dahia PLM, Sill H, Toledo SPA, Goldman JM, Cross NCP. Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas [Internet]. Clinical Endocrinology. 1996 ; 45( 1): 93-96.[citado 2024 set. 28 ] Available from: https://doi.org/10.1046/j.1365-2265.1996.00762.x
Artigo de periodico
Letters to the editors (1994)
Medeiros Neto, Geraldo Antônio
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
MEDEIROS NETO, Geraldo Antônio. Letters to the editors. Clinical Endocrinology, v. 40, n. 3 , p. 435, 1994Tradução . . Acesso em: 28 set. 2024.
APA
Medeiros Neto, G. A. (1994). Letters to the editors. Clinical Endocrinology, 40( 3 ), 435.
NLM
Medeiros Neto GA. Letters to the editors. Clinical Endocrinology. 1994 ;40( 3 ): 435.[citado 2024 set. 28 ]
Vancouver
Medeiros Neto GA. Letters to the editors. Clinical Endocrinology. 1994 ;40( 3 ): 435.[citado 2024 set. 28 ]
Artigo de periodico
Desmopressin stimulation test in the differential diagnosis of cushing's syndrome (1993)
Malerbi, D A; Mendonça, B. B.; Liberman, Bernardo; Toledo, S. P. A.; Corradini, M C M; Cunha Neto, M B C; Fragoso, M C B V; Wajchenberg, B L
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MALERBI, D A et al. Desmopressin stimulation test in the differential diagnosis of cushing's syndrome. Clinical Endocrinology, v. 38, n. 5 , p. 463-72, 1993Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.1993.tb00341.x. Acesso em: 28 set. 2024.
APA
Malerbi, D. A., Mendonça, B. B., Liberman, B., Toledo, S. P. A., Corradini, M. C. M., Cunha Neto, M. B. C., et al. (1993). Desmopressin stimulation test in the differential diagnosis of cushing's syndrome. Clinical Endocrinology, 38( 5 ), 463-72. doi:10.1111/j.1365-2265.1993.tb00341.x
NLM
Malerbi DA, Mendonça BB, Liberman B, Toledo SPA, Corradini MCM, Cunha Neto MBC, Fragoso MCBV, Wajchenberg BL. Desmopressin stimulation test in the differential diagnosis of cushing's syndrome [Internet]. Clinical Endocrinology. 1993 ;38( 5 ): 463-72.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1365-2265.1993.tb00341.x
Vancouver
Malerbi DA, Mendonça BB, Liberman B, Toledo SPA, Corradini MCM, Cunha Neto MBC, Fragoso MCBV, Wajchenberg BL. Desmopressin stimulation test in the differential diagnosis of cushing's syndrome [Internet]. Clinical Endocrinology. 1993 ;38( 5 ): 463-72.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1365-2265.1993.tb00341.x
Parte de monografia/livro
Extra endocrine actions of 1,25-dihydroxyvitamin 'D IND.3' determination of specific receptors in human leukemic cells (1988)
Feldman, J; Sonohara, Shigueko; Federico, Miriam Hatsue Honda; Leite, M O R; Brentani, Maria Mitzi
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FELDMAN, J et al. Extra endocrine actions of 1,25-dihydroxyvitamin 'D IND.3' determination of specific receptors in human leukemic cells. Clinical Endocrinology. Tradução . Amsterdam: Elsevier, 1988. . . Acesso em: 28 set. 2024.
APA
Feldman, J., Sonohara, S., Federico, M. H. H., Leite, M. O. R., & Brentani, M. M. (1988). Extra endocrine actions of 1,25-dihydroxyvitamin 'D IND.3' determination of specific receptors in human leukemic cells. In Clinical Endocrinology. Amsterdam: Elsevier.
NLM
Feldman J, Sonohara S, Federico MHH, Leite MOR, Brentani MM. Extra endocrine actions of 1,25-dihydroxyvitamin 'D IND.3' determination of specific receptors in human leukemic cells. In: Clinical Endocrinology. Amsterdam: Elsevier; 1988. [citado 2024 set. 28 ]
Vancouver
Feldman J, Sonohara S, Federico MHH, Leite MOR, Brentani MM. Extra endocrine actions of 1,25-dihydroxyvitamin 'D IND.3' determination of specific receptors in human leukemic cells. In: Clinical Endocrinology. Amsterdam: Elsevier; 1988. [citado 2024 set. 28 ]
Parte de monografia/livro
Effect of injectable cyproterone acetate on plasma testosterone fractionation in hirsute patients (1988)
Marcondes, J A M; Luthold, W W; Wajchenberg, B L
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARCONDES, J A M e LUTHOLD, W W e WAJCHENBERG, B L. Effect of injectable cyproterone acetate on plasma testosterone fractionation in hirsute patients. Clinical Endocrinology. Tradução . Amsterdam: Elsevier, 1988. . . Acesso em: 28 set. 2024.
APA
Marcondes, J. A. M., Luthold, W. W., & Wajchenberg, B. L. (1988). Effect of injectable cyproterone acetate on plasma testosterone fractionation in hirsute patients. In Clinical Endocrinology. Amsterdam: Elsevier.
NLM
Marcondes JAM, Luthold WW, Wajchenberg BL. Effect of injectable cyproterone acetate on plasma testosterone fractionation in hirsute patients. In: Clinical Endocrinology. Amsterdam: Elsevier; 1988. [citado 2024 set. 28 ]
Vancouver
Marcondes JAM, Luthold WW, Wajchenberg BL. Effect of injectable cyproterone acetate on plasma testosterone fractionation in hirsute patients. In: Clinical Endocrinology. Amsterdam: Elsevier; 1988. [citado 2024 set. 28 ]
Artigo de periodico
Glucocorticoids and glucose metabolism ; hepatic glucose production in untreated addisonian patients and on two different levels of glucocorticoid administration (1988)
Malerli, D; Liberman, Bernardo; Giurno Filho, A; Giannella Neto, D; Wajchenberg, B L
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MALERLI, D et al. Glucocorticoids and glucose metabolism ; hepatic glucose production in untreated addisonian patients and on two different levels of glucocorticoid administration. Clinical Endocrinology, v. 28, p. 415-22, 1988Tradução . . Acesso em: 28 set. 2024.
APA
Malerli, D., Liberman, B., Giurno Filho, A., Giannella Neto, D., & Wajchenberg, B. L. (1988). Glucocorticoids and glucose metabolism ; hepatic glucose production in untreated addisonian patients and on two different levels of glucocorticoid administration. Clinical Endocrinology, 28, 415-22.
NLM
Malerli D, Liberman B, Giurno Filho A, Giannella Neto D, Wajchenberg BL. Glucocorticoids and glucose metabolism ; hepatic glucose production in untreated addisonian patients and on two different levels of glucocorticoid administration. Clinical Endocrinology. 1988 ;28 415-22.[citado 2024 set. 28 ]
Vancouver
Malerli D, Liberman B, Giurno Filho A, Giannella Neto D, Wajchenberg BL. Glucocorticoids and glucose metabolism ; hepatic glucose production in untreated addisonian patients and on two different levels of glucocorticoid administration. Clinical Endocrinology. 1988 ;28 415-22.[citado 2024 set. 28 ]

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