Fonte: Journal of pediatric endocrinology and metabolism. Nome do evento: Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP). Unidade: FM
Assuntos: HIPERPLASIAS, HIDROXILASE, RESUMOS (CONGRESSOS)
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ABNT
PARENTE, E. B. et al. Final height in female patients with congenital adrenal hyperplasia due to 21-hydroxilase deficiency treated with cortisone acetate. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 23 ago. 2024. , 2004APA
Parente, E. B., Marquezine, G., Madureira, A. C., Brenilha, E. M. L., Ueti, R. C., Arnhold, I. J. P., et al. (2004). Final height in female patients with congenital adrenal hyperplasia due to 21-hydroxilase deficiency treated with cortisone acetate. Journal of pediatric endocrinology and metabolism. London: Faculdade de Medicina, Universidade de São Paulo.NLM
Parente EB, Marquezine G, Madureira AC, Brenilha EML, Ueti RC, Arnhold IJP, Mendonça BB, Bachega TASS. Final height in female patients with congenital adrenal hyperplasia due to 21-hydroxilase deficiency treated with cortisone acetate. Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1356.[citado 2024 ago. 23 ]Vancouver
Parente EB, Marquezine G, Madureira AC, Brenilha EML, Ueti RC, Arnhold IJP, Mendonça BB, Bachega TASS. Final height in female patients with congenital adrenal hyperplasia due to 21-hydroxilase deficiency treated with cortisone acetate. Journal of pediatric endocrinology and metabolism. 2004 ; 17( suppl.5): 1356.[citado 2024 ago. 23 ]
