High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screening (2019)
- Authors:
- Autor USP: BACHEGA, TÂNIA APARECIDA SARTORI SANCHEZ - FM
- Unidade: FM
- DOI: 10.1515/jpem-2018-0398
- Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA; PROGESTERONA; ESTEROIDE HIDROXILASE; TRIAGEM; RECÉM-NASCIDO
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of pediatric endocrinology & metabolism
- ISSN: 0334-018X
- Volume/Número/Paginação/Ano: v. 32, n. 5, p. 499-504, 2019
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
CASTRO, Patricia S et al. High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screening. Journal of pediatric endocrinology & metabolism, v. 32, n. 5, p. 499-504, 2019Tradução . . Disponível em: https://doi.org/10.1515/jpem-2018-0398. Acesso em: 04 maio 2024. -
APA
Castro, P. S., Rassi, T. O., Araujo, R. F., Pezzuti, I. L., Rodrigues, A. S., Bachega, T. A. S. S., & Silva, I. N. (2019). High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screening. Journal of pediatric endocrinology & metabolism, 32( 5), 499-504. doi:10.1515/jpem-2018-0398 -
NLM
Castro PS, Rassi TO, Araujo RF, Pezzuti IL, Rodrigues AS, Bachega TASS, Silva IN. High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screening [Internet]. Journal of pediatric endocrinology & metabolism. 2019 ; 32( 5): 499-504.[citado 2024 maio 04 ] Available from: https://doi.org/10.1515/jpem-2018-0398 -
Vancouver
Castro PS, Rassi TO, Araujo RF, Pezzuti IL, Rodrigues AS, Bachega TASS, Silva IN. High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screening [Internet]. Journal of pediatric endocrinology & metabolism. 2019 ; 32( 5): 499-504.[citado 2024 maio 04 ] Available from: https://doi.org/10.1515/jpem-2018-0398 - Hiperplasia adrenal congênita
- Molecular -genetic causes underlying primary adrenal insufficiency. [Editorial]: current insights into diagnosis and treatment
- Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency
- Guidelines for the Development of Comprehensive Care Centers for Congenital Adrenal Hyperplasia: Guidance from the CARES Foundation Initiative
- Insuficiência adrenal
- Low adrenomedullary function predicts acute illness in infants with classical congenital adrenal hyperplasia
- Mutações no gene da 21-hidroxilase em pacientes com hiperplasia adrenal congênita por deficiência da 21-hidroxilase, formas clássica e não clássica
- The Actual Incidence of Congenital Adrenal Hyperplasia in Brazil May Not be as High as Inferred - An Estimate Based on a Public Neonatal Screening Program in the State of Goiás
- Effects of endocrine disruptors in the development of the female reproductive tract
- Hiperplasia congênita das supras-renais
Informações sobre o DOI: 10.1515/jpem-2018-0398 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
