ReP USP - Resultado da busca

High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screening (2019)

Castro, Patricia S; Rassi, Tatiana O; Araujo, Raquel F; Pezzuti, Isabela L; Rodrigues, Andresa S; Bachega, Tânia Aparecida Sartori Sanchez; Silva, Ivani N

Source: Journal of pediatric endocrinology & metabolism. Unidade: FM

Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA, PROGESTERONA, ESTEROIDE HIDROXILASE, TRIAGEM, RECÉM-NASCIDO

A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

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: 18 nov. 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 nov. 18 ] 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 nov. 18 ] Available from: https://doi.org/10.1515/jpem-2018-0398

Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a homozygous 25 BP duplication (NT 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon predicted by molecular modeling (2008)

Martin, Regina M.; Oliveira, Paulo S.; Costa, Elaine M. F.; Arnhold, Ivo J. P.; Mendonça, Berenice Bilharinho de

Source: Arquivos brasileiros de endocrinologia e metabologia. Unidade: FM

Subjects: HIDROXILASE (DEFICIÊNCIA), HIPERTENSÃO, HIPERPLASIA SUPRARRENAL CONGÊNITA, PROGESTERONA, MODELAGEM MOLECULAR

USP Schools

ReP

Filtros

Authors

Subjects