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 do periódico: 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: 18 set. 2024. -
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 2024 set. 18 ] 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 2024 set. 18 ] Available from: https://doi.org/10.1210/clinem/dgab293 - Genetics basis for GnRH-dependent pubertal disorders in humans
- KISS1R Intracellular Trafficking and Degradation: Effect of the Arg386Pro Disease-Associated Mutation
- New genetic factors implicated in human GnRH-dependent precocius puberty: the role of kisspeptin system
- A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations
- Disorders of Sex Development and Hypogonadism [Editorial]: Genetics, Mechanism, and Therapies
- An ancient founder mutation in PROKR2 impairs human reproduction
- Puberty: When is it normal? [Editorial]
- Hipogonadismo
- Mutações ativadoras no gene do receptor do hormônio luteinizante em meninos brasileiros com testotoxicose
- Evidence of the Importance of the First Intracellular Loop of Prokineticin Receptor 2 in Receptor Function
Informações sobre o DOI: 10.1210/clinem/dgab293 (Fonte: oaDOI API)
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