A novel mutation in the vasopressin-neurofisin II gene (Ala68Pro) associated with familial autosomal dominant neurohypophyseal diabetes insipidus (2002)
- Authors:
- USP affiliated authors: MOREIRA, AYRTON CUSTODIO - FMRP ; RODRIGUES, JOSE ANTUNES - FMRP ; CASTRO, MARGARET DE - FMRP
- Unidade: FMRP
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: Endocrine Society
- Publisher place: San Francisco
- Date published: 2002
- Source:
- Título: Program and Abstracts
- Conference titles: Annual Meeting of the Endocrine Society
-
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: 28 dez. 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 dez. 28 ] -
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 dez. 28 ] - Ocitocina (OT) na secreção de ACTH em ratos adrenalectomizados (ADX)
- Nova mutação do gene da vasopressina-neurofisina II (Ala68Pro) associada à forma familiar de diabetes insípido central
- Pituitary-adrenal axis response to acute and chronic salt load in functionally neurolobectomized rats
- Pituitary-adrenal axis (HPA) response to stress in functionally neurolobectomized rats
- Eixo HHA e vasopressina (AVP) em ratos submetidos à adrenalectomia (ADX) e estresse
- Progressive decline of vasopressin secretion in familial autossomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene
- Expression of clock-related genes in response to different restricted feeding patterns
- O gene homeobox Hexx1 nos defeitos da linha média cerebral (DLMC)
- Diagnóstico laboratorial da Síndorme de Cushing
- Efetio fundador da mutação Q356X no gene CYP11B1 em pacientes com deficiência da '11beta'- hidroxilase
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