Brain MRI in girls with central precocious puberty: a time for new approaches comment (2021)
- Authors:
- Autor USP: XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- DOI: 10.1210/clinem/dgab293
- Subjects: PUBERDADE PRECOCE; RESSONÂNCIA MAGNÉTICA; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2021
- Source:
- Título: Journal of clinical endocrinology & metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 106, n. 7, p. E2806-E2808, 2021
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
CANTON, Ana Pinheiro Machado e XAVIER, Ana Claudia Latronico. Brain MRI in girls with central precocious puberty: a time for new approaches comment. Journal of clinical endocrinology & metabolism, v. 106, n. 7, p. E2806-E2808, 2021Tradução . . Disponível em: https://doi.org/10.1210/clinem/dgab293. Acesso em: 10 jan. 2026. -
APA
Canton, A. P. M., & Xavier, A. C. L. (2021). Brain MRI in girls with central precocious puberty: a time for new approaches comment. Journal of clinical endocrinology & metabolism, 106( 7), E2806-E2808. doi:10.1210/clinem/dgab293 -
NLM
Canton APM, Xavier ACL. Brain MRI in girls with central precocious puberty: a time for new approaches comment [Internet]. Journal of clinical endocrinology & metabolism. 2021 ; 106( 7): E2806-E2808.[citado 2026 jan. 10 ] Available from: https://doi.org/10.1210/clinem/dgab293 -
Vancouver
Canton APM, Xavier ACL. Brain MRI in girls with central precocious puberty: a time for new approaches comment [Internet]. Journal of clinical endocrinology & metabolism. 2021 ; 106( 7): E2806-E2808.[citado 2026 jan. 10 ] Available from: https://doi.org/10.1210/clinem/dgab293 - A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties
- Normal bone mass and normocalcemia in adulthood despite homozygous vitamin D receptor mutations
- Puberdade precoce
- MicroRNA era: The importance for diagnosis and prognosis of adrenocortical tumors
- An ancient founder mutation in PROKR2 impairs human reproduction
- Mutational analysis of the genes encoding RFAmide-related peptide-3 the human orthologue of gonadotrophin-inhibitory hormone, and its receptor (GPR 147) in patients with gonadotrophin-releasing hormone-dependent pubertal disorders
- Mutation Analysis of EDG2 (LPAR1) and GPR26 in the Patients with Precocious Puberty
- A new pathway in the control of the initiation of puberty: the MKRN3 gene
- Insulin-like growth factor system on adrenocortical tumorigenesis
- Aspectos clínicos e moleculares do hipogonadismo hipogonadotrófico isolado congênito
Informações sobre o DOI: 10.1210/clinem/dgab293 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
