Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients (2013)
- Autores:
- Autores USP: MENDONÇA, BERENICE BILHARINHO DE - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1159/000353762
- Assuntos: ENDOCRINOPATIAS; HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA); TRANSTORNOS DO CRESCIMENTO
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 80, suppl. 1, p. 295, res. P2-d1-952, 2013
- Nome do evento: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
LIDO, Andria C. V. et al. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 30 set. 2024. , 2013 -
APA
Lido, A. C. V., França, M. M., Otto, A. P., Carvalho, L. R., Mendonça, B. B. de, Arnhold, I. J. P., & Jorge, A. A. de L. (2013). Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762 -
NLM
Lido ACV, França MM, Otto AP, Carvalho LR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2024 set. 30 ] Available from: https://doi.org/10.1159/000353762 -
Vancouver
Lido ACV, França MM, Otto AP, Carvalho LR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2024 set. 30 ] Available from: https://doi.org/10.1159/000353762 - Investigação genética
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- Exome sequencing reveals the POLR3H gene as a novel cause of primary ovarian insufficiency
- Usefulness of MLPA in the detection of SHOX deletions
- Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE)
- The Effect of Transdermic Dihydrotestosterone Gel Treatment on Penile Size: Experience with Fifteen Patients
- Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly
- Role of GLI2 in hypopituitarism phenotype
- Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation
Informações sobre o DOI: 10.1159/000353762 (Fonte: oaDOI API)
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