Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
The Journal of Clinical Endocrinology and Metabolism|October 7, 2016
Randomized Trial of Aromatase Inhibitors, Growth Hormone, or Combination in Pubertal Boys with Idiopathic, Short StatureNelly Mauras, Judith L Ross, Priscila Gagliardi, et al.
Hormone Research in Paediatrics|March 2, 2019
Quality of Life in Adolescent Boys with Idiopathic Short Stature: Positive Impact of Growth Hormone and Aromatase InhibitorsMonika Bullinger, Janika Bloemeke, Veronica Mericq, et al.
Clinical Endocrinology|October 4, 2018
Impact of route of administration on genotoxic oestrogens concentrations using oral vs transdermal oestradiol in girls with Turner syndromeNelly Mauras, Lournaris Torres-Santiago, Richard Santen, et al.
Hormone Research in Paediatrics|October 27, 2021
Primary Ovarian Failure in Addition to Classical Clinical Features of Coats Plus Syndrome in a Female Carrying 2 Truncating Variants of CTC1Joel Riquelme, Sanami Takada, Tessa van Dijk, et al.
The Journal of Clinical Endocrinology and Metabolism|November 18, 2021
Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type IbAngelo Milioto, Monica Reyes, Patrick Hanna, et al.
European Journal of Endocrinology|March 2, 2022
Biallelic POC1A variants cause syndromic severe insulin resistance with muscle crampsVeronica Mericq, Isabel Huang-Doran, Dhekra Al-Naqeb, et al.
Hormone Research in Paediatrics|September 5, 2015
A Deletion of More than 800 kb Is the Most Recurrent Mutation in Chilean Patients with SHOX Gene DefectsHelena Poggi, Alejandra Vera, Carolina Avalos, et al.
BMC Pediatrics|July 21, 2011
Latin American consensus: children born small for gestational ageMargaret C S Boguszewski, Veronica Mericq, Ignacio Bergada, et al.
Pediatric Endocrinology Reviews : PER|March 9, 2012
Growth hormone and treatment outcomes: expert review of current clinical practiceFernando Cassorla, Stefano Cianfarani, Fritz Haverkamp, et al.
Human Mutation|February 24, 2015
Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short statureSophie R Wang, Christina M Jacobsen, Heather Carmichael, et al.
Pageof 6