Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes (2002)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; ARNHOLD, IVO J. P. - FM ; LEITE, CLAUDIA DA COSTA - FM
- Unidade: FM
- Subjects: ENDOCRINOLOGIA; GENÉTICA MOLECULAR
- Language: Inglês
- Imprenta:
- Source:
- Título: The Journal of Clinical Endocrinology & Metabolism
- Volume/Número/Paginação/Ano: v. 87, n. 11, p. 5076-5084, 2002
-
ABNT
OSORIO, Maria Geralda F. et al. Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes. The Journal of Clinical Endocrinology & Metabolism, v. 87, n. 11, p. 5076-5084, 2002Tradução . . Acesso em: 27 jan. 2026. -
APA
Osorio, M. G. F., Marui, S., Jorge, A. A. L., Latronico, A. C., Lo, L. S. S., Leite, C. C., et al. (2002). Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes. The Journal of Clinical Endocrinology & Metabolism, 87( 11), 5076-5084. -
NLM
Osorio MGF, Marui S, Jorge AAL, Latronico AC, Lo LSS, Leite CC, Estefan V, Mendonça BB, Arnhold IJP. Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 11): 5076-5084.[citado 2026 jan. 27 ] -
Vancouver
Osorio MGF, Marui S, Jorge AAL, Latronico AC, Lo LSS, Leite CC, Estefan V, Mendonça BB, Arnhold IJP. Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 11): 5076-5084.[citado 2026 jan. 27 ] - Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe
- Ressonancia magnética e função hipofisaria em pacientes com deficiência de GH com E sem mutações nos genes GH-1, receptor do GHRH-R e HESX-1
- Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations
- Novel heterozygous nonsesns GLI2 mutations in patientswith hypopituitarism and ectopic posterios pituitary lobe without holoprosencephaly
- Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Microconversão no promotor do gene CYP21A2 envolvendo os sítios de ligação dos fatores de transcrição Sp1 e ASP: nova etiologia molecular da deficiência de 21-hidroxilase (21OHD)
- Molecular analysis of two distinct candidate genes (GABRA1 and NPY-Y1) that could be implicated in the human puberty timing
- Nova etiologia da deficiência da 21OH: microconversão nos sítios de liga dos fatores de transcrição Sp1 e ASP no promotor do gene CYP21A2
- Clinical and molecular heterogeneity of hypogonadotropic hypogonadism (HH):: importance of olfactory system assessment in the differential diagnosis
- Reprodutive outcome of women with 21-Hydroxylase (21-OH) deficient non classic adrenal hyperplasia (NCAH):: a multicenter study
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas