Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene (2000)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Estados Unidos
- Date published: 2000
- Source:
- Título do periódico: The Journal of Clinical Endocrinology & Metabolism
- Volume/Número/Paginação/Ano: v. 85, n. 01, p. 390-397, 2000
-
ABNT
PERNASETTI, Flavia et al. Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. The Journal of Clinical Endocrinology & Metabolism, v. 85, n. 01, p. 390-397, 2000Tradução . . Acesso em: 22 maio 2024. -
APA
Pernasetti, F., Toledo, S. P. A., Vasilyev, V. V., Hayashida, C. Y., Cogan, J. D., Ferrari, C., et al. (2000). Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. The Journal of Clinical Endocrinology & Metabolism, 85( 01), 390-397. -
NLM
Pernasetti F, Toledo SPA, Vasilyev VV, Hayashida CY, Cogan JD, Ferrari C, Lourenço DM, Mellon PL. Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. The Journal of Clinical Endocrinology & Metabolism. 2000 ; 85( 01): 390-397.[citado 2024 maio 22 ] -
Vancouver
Pernasetti F, Toledo SPA, Vasilyev VV, Hayashida CY, Cogan JD, Ferrari C, Lourenço DM, Mellon PL. Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. The Journal of Clinical Endocrinology & Metabolism. 2000 ; 85( 01): 390-397.[citado 2024 maio 22 ] - Carcinoma medular de tireoide
- Sindrome hereditaria caracterizada por micropenis, hipoandrogenismo e niveis sericos altos de gonadotrofinas devido a disturbio primario nas celulas de leydig, associada a testiculos de tamanho normal e ausencia de ambiguidade genital: uma provavel nova entidade clinica
- Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female
- Missense mutation in the lh receptor gene causas leydig cell hypoplasia
- Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations
- Neoplasias endócrinas múltiplas
- Relato de caso de tireotropinoma
- Germline mutations in TMEM127 confer susceptibility to pheochromocytoma [Carta]
- Screening of RET gene mutations in multiple endocrine neoplasia type-2 using Conformation Sensitive Gel Electrophoresis (CSGE)
- Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
