Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective (2019)
- Authors:
- Autor USP: JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1159/000502231
- Subjects: TRANSTORNOS DO CRESCIMENTO; HORMÔNIO DO CRESCIMENTO; CRIANÇAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Hormone research in paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 92, n. 1, p. 1-14, 2019
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by-nc-nd
-
ABNT
COLLETT-SOLBERG, Paulo F et al. Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective. Hormone research in paediatrics, v. 92, n. 1, p. 1-14, 2019Tradução . . Disponível em: https://doi.org/10.1159/000502231. Acesso em: 11 jan. 2026. -
APA
Collett-solberg, P. F., Ambler, G., Backeljauw, P. F., Bidlingmaier, M., Biller, B. M. K., Boguszewski, M. C. S., et al. (2019). Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective. Hormone research in paediatrics, 92( 1), 1-14. doi:10.1159/000502231 -
NLM
Collett-solberg PF, Ambler G, Backeljauw PF, Bidlingmaier M, Biller BMK, Boguszewski MCS, Cheung PT, Choong CSY, Cohen LE, Jorge AA de L. Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective [Internet]. Hormone research in paediatrics. 2019 ; 92( 1): 1-14.[citado 2026 jan. 11 ] Available from: https://doi.org/10.1159/000502231 -
Vancouver
Collett-solberg PF, Ambler G, Backeljauw PF, Bidlingmaier M, Biller BMK, Boguszewski MCS, Cheung PT, Choong CSY, Cohen LE, Jorge AA de L. Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective [Internet]. Hormone research in paediatrics. 2019 ; 92( 1): 1-14.[citado 2026 jan. 11 ] Available from: https://doi.org/10.1159/000502231 - Influence of growth hormone receptor (GHR) exon 3 and -202A/C IGFBP-3 genetic polymorphisms on clinical and biochemical features and therapeutic outcome of patients with acromegaly
- Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders
- Abordagem clínica
- Whole Exome Sequencing in the Investigation of Growth Disorders, Including Patients with Primary IGF-1 Deficiency
- A Novel Homologous Model for Gene Therapy of Dwarfism by Non-Viral Transfer of the Mouse Growth Hormone Gene into Immunocompetent Dwarf Mice
- Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2
- Aplicações clínicas dos testes genéticos em endocrinologia
- A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings
- Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants
- Clinical and molecular analysis of pubertal control in a cohort of silver-russel and temple syndromes patients
Informações sobre o DOI: 10.1159/000502231 (Fonte: oaDOI API)
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