Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review (2021)
- Authors:
- Dantas, Naiara Castelo Branco
- Braz, Adriana F.
- Malaquias, Alexsandra
- Lemos-Marini, Sofia - Universidade Estadual de Campinas (UNICAMP)
- Arnhold, Ivo Jorge Prado
- Ramos, Ester Silveira
- Antonini, Sonir Roberto Rauber
- Guerra-Junior, Gil - Universidade Estadual de Campinas (UNICAMP)
- Mendonça, Berenice Bilharinho de
- Jorge, Alexander Augusto de Lima
- Scalco, Renata C.
- USP affiliated authors: ARNHOLD, IVO JORGE PRADO - FM ; RAMOS, ESTER SILVEIRA - FMRP ; ANTONINI, SONIR ROBERTO RAUBER - FMRP ; MENDONÇA, BERENICE BILHARINHO DE - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; DANTAS, NAIARA CASTELO BRANCO - FM
- Unidades: FM; FMRP
- DOI: 10.1159/000516869
- Subjects: HORMÔNIO DO CRESCIMENTO; ADULTOS; HORMÔNIOS
- Keywords: Adult height; Growth hormone therapy; Turner syndrome
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 94, n. 1-2, p. 63-70, 2021
- Status:
- Artigo possui versão em acesso aberto em repositório (Green Open Access)
- Versão do Documento:
- Versão submetida (Pré-print)
- Acessar versão aberta:
-
ABNT
DANTAS, Naiara Castelo Branco et al. Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review. Hormone Research in Paediatrics, v. 94, n. 1-2, p. 63-70, 2021Tradução . . Disponível em: https://doi.org/10.1159/000516869. Acesso em: 10 abr. 2026. -
APA
Dantas, N. C. B., Braz, A. F., Malaquias, A., Lemos-Marini, S., Arnhold, I. J. P., Ramos, E. S., et al. (2021). Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review. Hormone Research in Paediatrics, 94( 1-2), 63-70. doi:10.1159/000516869 -
NLM
Dantas NCB, Braz AF, Malaquias A, Lemos-Marini S, Arnhold IJP, Ramos ES, Antonini SRR, Guerra-Junior G, Mendonça BB de, Jorge AA de L, Scalco RC. Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review [Internet]. Hormone Research in Paediatrics. 2021 ; 94( 1-2): 63-70.[citado 2026 abr. 10 ] Available from: https://doi.org/10.1159/000516869 -
Vancouver
Dantas NCB, Braz AF, Malaquias A, Lemos-Marini S, Arnhold IJP, Ramos ES, Antonini SRR, Guerra-Junior G, Mendonça BB de, Jorge AA de L, Scalco RC. Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review [Internet]. Hormone Research in Paediatrics. 2021 ; 94( 1-2): 63-70.[citado 2026 abr. 10 ] Available from: https://doi.org/10.1159/000516869 - Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and - 202 A/C IGFBP3 variants an treatment outcomes of children with severe GH deficiency
- Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism
- The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome
- Adult Height of Patients with <it><bold>SHOX</it></bold> Haploinsufficiency with or without GH Therapy: A Real-World Single-Center Study
- Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability
- Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
- Baixa estatura desproporcional por mutações no gene SHOX
- Novel Mutations (p.G6R and p.R511W) in IGF1R Gene in Children Born Small for Gestational Age (SGA) Without Catch-up Growth
- Growth Hormone (GH) Pharmacogenetics: Positive Influence of GH Receptor (GHR) Exon 3 Deleted Allele (d3) on First-year Growth Velocity and Final Height in Patients with Turner Syndrome (TS) Treated with Recombinant Human GH (rhGH)
- Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients
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