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The Journal of Clinical Endocrinology and Metabolism
|
September 27, 2007
Polymorphisms identified in the upstream core polyadenylation signal of IGF1 gene exon 6 do not cause pre- and postnatal growth impairment
Debora C Coutinho, Rocio R D Coletta, Elaine M F Costa, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
August 25, 2014
Are CYP1A1, CYP17 and CYP1B1 mutation genes involved on girls with precocious puberty? A pilot study
Cezar Noboru Matsuzaki, José Maria Soares Júnior, Durval Damiani, et al.
Frontiers in Pediatrics
|
June 10, 2021
The Cost-Effectiveness of Congenital Adrenal Hyperplasia Newborn Screening in Brazil: A Comparison Between Screened and Unscreened Cohorts
Mirela Costa de Miranda, Luciana Bertocco de Paiva Haddad, Evelinda Trindade, et al.
Frontiers in Endocrinology
|
October 6, 2025
12-month outcomes of GLP - 1 in severe pediatric obesity: real-world data
Louise Cominato, Mariana L Resende, Natalia Bernardes, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo
|
October 27, 2018
PRADER-WILLI SYNDROME: WHAT IS THE GENERAL PEDIATRICIAN SUPPOSED TO DO? - A REVIEW
Caroline Buff Gouveia Passone, Paula Lage Pasqualucci, Ruth Rocha Franco, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 8, 2006
Diagnosis of 5alpha-reductase type 2 deficiency: contribution of anti-Müllerian hormone evaluation
Eliana G Stuchi-Perez, Christine Hackel, Luiz Eduardo C Oliveira, et al.
BMC Pediatrics
|
July 21, 2011
Latin American consensus: children born small for gestational age
Margaret C S Boguszewski, Veronica Mericq, Ignacio Bergada, et al.
Frontiers in Endocrinology
|
July 5, 2024
Puberty in girls with Prader-Willi syndrome: cohort evaluation and clinical recommendations in a Latin American tertiary center
Caroline Gouveia Buff Passone, Luciana Felipe Ferrer Aragão, Ruth Rocha Franco, et al.
European Journal of Endocrinology
|
May 18, 2016
Molecular CYP21A2 diagnosis in 480 Brazilian patients with congenital adrenal hyperplasia before newborn screening introduction
Daniel F de Carvalho, Mirela C Miranda, Larissa G Gomes, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2014
The E180splice mutation in the GHR gene causing Laron syndrome: witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?
Fernanda T Gonçalves, Cintia Fridman, Emília M Pinto, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 75) with videos related to
Sort By:
Page
of 8
The Journal of Clinical Endocrinology and Metabolism
|
September 27, 2007
Polymorphisms identified in the upstream core polyadenylation signal of IGF1 gene exon 6 do not cause pre- and postnatal growth impairment
Debora C Coutinho, Rocio R D Coletta, Elaine M F Costa, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
August 25, 2014
Are CYP1A1, CYP17 and CYP1B1 mutation genes involved on girls with precocious puberty? A pilot study
Cezar Noboru Matsuzaki, José Maria Soares Júnior, Durval Damiani, et al.
Frontiers in Pediatrics
|
June 10, 2021
The Cost-Effectiveness of Congenital Adrenal Hyperplasia Newborn Screening in Brazil: A Comparison Between Screened and Unscreened Cohorts
Mirela Costa de Miranda, Luciana Bertocco de Paiva Haddad, Evelinda Trindade, et al.
Frontiers in Endocrinology
|
October 6, 2025
12-month outcomes of GLP - 1 in severe pediatric obesity: real-world data
Louise Cominato, Mariana L Resende, Natalia Bernardes, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo
|
October 27, 2018
PRADER-WILLI SYNDROME: WHAT IS THE GENERAL PEDIATRICIAN SUPPOSED TO DO? - A REVIEW
Caroline Buff Gouveia Passone, Paula Lage Pasqualucci, Ruth Rocha Franco, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 8, 2006
Diagnosis of 5alpha-reductase type 2 deficiency: contribution of anti-Müllerian hormone evaluation
Eliana G Stuchi-Perez, Christine Hackel, Luiz Eduardo C Oliveira, et al.
BMC Pediatrics
|
July 21, 2011
Latin American consensus: children born small for gestational age
Margaret C S Boguszewski, Veronica Mericq, Ignacio Bergada, et al.
Frontiers in Endocrinology
|
July 5, 2024
Puberty in girls with Prader-Willi syndrome: cohort evaluation and clinical recommendations in a Latin American tertiary center
Caroline Gouveia Buff Passone, Luciana Felipe Ferrer Aragão, Ruth Rocha Franco, et al.
European Journal of Endocrinology
|
May 18, 2016
Molecular CYP21A2 diagnosis in 480 Brazilian patients with congenital adrenal hyperplasia before newborn screening introduction
Daniel F de Carvalho, Mirela C Miranda, Larissa G Gomes, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2014
The E180splice mutation in the GHR gene causing Laron syndrome: witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?
Fernanda T Gonçalves, Cintia Fridman, Emília M Pinto, et al.
Page
of 8