Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects (2015)
- Authors:
- USP affiliated authors: MARTINELLI JUNIOR, CARLOS EDUARDO - FMRP ; MOREIRA, AYRTON CUSTODIO - FMRP ; SANTOS, ANTONIO CARLOS DOS - FMRP ; CASTRO, MARGARET DE - FMRP ; ANTONINI, SONIR ROBERTO RAUBER - FMRP
- Unidade: FMRP
- DOI: 10.1111/cen.12565
- Subjects: NEOPLASIAS CRANIANAS; EXPRESSÃO GÊNICA
- Language: Inglês
- Imprenta:
- Publisher place: West Sussex
- Date published: 2015
- Source:
- Título: Clinical Endocrinology
- ISSN: 0300-0664
- Volume/Número/Paginação/Ano: v. 82, n. 4, p. 562-569, 2015
- Este artigo NÃO possui versão em acesso aberto
-
Status: Nenhuma versão em acesso aberto identificada -
ABNT
PAULO, Sabrina Soares et al. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects. Clinical Endocrinology, v. 82, n. 4, p. 562-569, 2015Tradução . . Disponível em: https://doi.org/10.1111/cen.12565. Acesso em: 15 mar. 2026. -
APA
Paulo, S. S., Fernandes-Rosa, F. L., Turatti, W., Coeli-Lacchini, F. B., Martinelli Junior, C. E., Nakiri, G. S., et al. (2015). Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects. Clinical Endocrinology, 82( 4), 562-569. doi:10.1111/cen.12565 -
NLM
Paulo SS, Fernandes-Rosa FL, Turatti W, Coeli-Lacchini FB, Martinelli Junior CE, Nakiri GS, Moreira AC, Santos AC dos, Castro M de, Antonini SRR. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects [Internet]. Clinical Endocrinology. 2015 ; 82( 4): 562-569.[citado 2026 mar. 15 ] Available from: https://doi.org/10.1111/cen.12565 -
Vancouver
Paulo SS, Fernandes-Rosa FL, Turatti W, Coeli-Lacchini FB, Martinelli Junior CE, Nakiri GS, Moreira AC, Santos AC dos, Castro M de, Antonini SRR. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects [Internet]. Clinical Endocrinology. 2015 ; 82( 4): 562-569.[citado 2026 mar. 15 ] Available from: https://doi.org/10.1111/cen.12565 - Análise dos genes SONIC HEDGEHOG (SHH) e GLI2 em pacientes com hipopituitarismo e/ou defeitos de linha média cerebral
- Salivary cortisol as a diagnostic tool of hypercortisolism in primary pigmented nodular adrenocortical disease (ppnad)
- Non-radioactive strategies on the diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency (CAH-210HD)
- OTX2 gene mutations are rare in patients with combined pituitary hormone deficiency (CPHD) and /or midline cerebral defects (MCD)
- Intermittent rhGH treatment as an alternative to rhlGF-I in a boy with GH1 macrodeletion
- Pituitary enlargement due to partial IGF-I insensitivity
- Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients
- Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care
- Mechanisms in endocrinology: a sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing’s syndrome
- Mutações no gene GHRHR em pacientes com deficiência isolada de GH(DIGH)
Informações sobre a disponibilidade de versões do artigo em acesso aberto coletadas automaticamente via oaDOI API (Unpaywall).
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas