Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2 (2017)
- Authors:
- Autor USP: JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1515/jpem-2016-0280
- Subjects: HORMÔNIO DO CRESCIMENTO; MUTAÇÃO GENÉTICA; ESTATUTO DA CRIANÇA E DO ADOLESCENTE; IMAGEM POR RESSONÂNCIA MAGNÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of pediatric endocrinology & metabolism
- ISSN: 0334-018X
- Volume/Número/Paginação/Ano: v. 30, n. 1, p. 111-116, 2017
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
VASQUES, Gabriela A. et al. Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2. Journal of pediatric endocrinology & metabolism, v. 30, n. 1, p. 111-116, 2017Tradução . . Disponível em: https://doi.org/10.1515/jpem-2016-0280. Acesso em: 21 jan. 2026. -
APA
Vasques, G. A., Hisado-Oliva, A., Funari, M. F. A., Lerario, A. M., Quedas, E. P. S., Solberg, P., et al. (2017). Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2. Journal of pediatric endocrinology & metabolism, 30( 1), 111-116. doi:10.1515/jpem-2016-0280 -
NLM
Vasques GA, Hisado-Oliva A, Funari MFA, Lerario AM, Quedas EPS, Solberg P, Heath KE, Jorge AAL. Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2 [Internet]. Journal of pediatric endocrinology & metabolism. 2017 ; 30( 1): 111-116.[citado 2026 jan. 21 ] Available from: https://doi.org/10.1515/jpem-2016-0280 -
Vancouver
Vasques GA, Hisado-Oliva A, Funari MFA, Lerario AM, Quedas EPS, Solberg P, Heath KE, Jorge AAL. Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2 [Internet]. Journal of pediatric endocrinology & metabolism. 2017 ; 30( 1): 111-116.[citado 2026 jan. 21 ] Available from: https://doi.org/10.1515/jpem-2016-0280 - Whole Exome Sequencing in the Investigation of Growth Disorders, Including Patients with Primary IGF-1 Deficiency
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- Abordagem clínica
- Hormone resistance and short stature: a journey through the pathways of hormone signaling
- Crescimento
- Management of endocrine disease: Diagnostic and therapeutic approach of tall stature
- A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism
- A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings
Informações sobre o DOI: 10.1515/jpem-2016-0280 (Fonte: oaDOI API)
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