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Filtros : "Mendonça, B. B." "2000" Limpar

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Artigo de periodico
Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions (2000)
Arnhold, I. J.; Oliveira, S. B.; Osorio, M G; Carrilho, A J F; Nicolau, Wilian; Bianco, Antônio Carlos; Mendonça, B. B.
Source: Journal of Endocrinological Investigation. Unidade: ICB
Assunto: FISIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARNHOLD, I. J. et al. Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions. Journal of Endocrinological Investigation, v. 23, p. 258-262, 2000Tradução . . Disponível em: https://doi.org/10.1007/bf03343719. Acesso em: 14 nov. 2024.
APA
Arnhold, I. J., Oliveira, S. B., Osorio, M. G., Carrilho, A. J. F., Nicolau, W., Bianco, A. C., & Mendonça, B. B. (2000). Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions. Journal of Endocrinological Investigation, 23, 258-262. doi:10.1007/bf03343719
NLM
Arnhold IJ, Oliveira SB, Osorio MG, Carrilho AJF, Nicolau W, Bianco AC, Mendonça BB. Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions [Internet]. Journal of Endocrinological Investigation. 2000 ; 23 258-262.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/bf03343719
Vancouver
Arnhold IJ, Oliveira SB, Osorio MG, Carrilho AJF, Nicolau W, Bianco AC, Mendonça BB. Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions [Internet]. Journal of Endocrinological Investigation. 2000 ; 23 258-262.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/bf03343719
Artigo de periodico
Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls (2000)
Marui, S.; Castro, Margaret de; Latronico, A. C.; Elias, Lucila Leico Kagohara; Arnhold, Ivo Jorge Prado; Moreira, Ayrton Custódio; Mendonça, B. B.
Source: Clinical Endocrinology. Unidade: FMRP
Subjects: ENDOCRINOLOGIA, HORMÔNIOS (METABOLISMO), DESENVOLVIMENTO FÍSICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARUI, S. et al. Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls. Clinical Endocrinology, v. 52, p. 67-75, 2000Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2000.00873.x. Acesso em: 14 nov. 2024.
APA
Marui, S., Castro, M. de, Latronico, A. C., Elias, L. L. K., Arnhold, I. J. P., Moreira, A. C., & Mendonça, B. B. (2000). Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls. Clinical Endocrinology, 52, 67-75. doi:10.1046/j.1365-2265.2000.00873.x
NLM
Marui S, Castro M de, Latronico AC, Elias LLK, Arnhold IJP, Moreira AC, Mendonça BB. Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls [Internet]. Clinical Endocrinology. 2000 ; 52 67-75.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1046/j.1365-2265.2000.00873.x
Vancouver
Marui S, Castro M de, Latronico AC, Elias LLK, Arnhold IJP, Moreira AC, Mendonça BB. Mutations in the type II 3'beta'-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls [Internet]. Clinical Endocrinology. 2000 ; 52 67-75.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1046/j.1365-2265.2000.00873.x

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