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Hormone Research in Paediatrics|April 10, 2014
17α-hydroxylase deficiency diagnosed in early infancy caused by a novel mutation of the CYP17A1 geneChristina Petri, Stefan A Wudy, Felix G Riepe, et al.Journal of the Endocrine Society|January 18, 2024
Urinary Androgens Provide Additional Evidence Related to Metabolism and Are Correlated With Serum Androgens in GirlsSasinya N Scott, Marvin Siguencia, Frank Z Stanczyk, et al.Clinical Chemistry and Laboratory Medicine|August 3, 2026
Mapping pediatric cardiac troponin testing worldwide: results from the IFCC survey on emerging applications, standardization needs and accessCatherine L Omosule, Tim Lang, Sharon M Geaghan, et al.Endocrine Connections|January 22, 2021
Sex-specific differences in HPA axis activity in VLBW preterm newbornsBritt J van Keulen, Michelle Romijn, Bibian van der Voorn, et al.Endocrine|March 8, 2022
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndromeMatthias K Auer, Wiebke Birnbaum, Michaela F Hartmann, et al.ACS Nano|May 24, 2017
Solitary Oxygen Dopant Emission from Carbon Nanotubes Modified by Dielectric MetasurfacesXuedan Ma, Anthony R James, Nicolai F Hartmann, et al.Pediatric Obesity|July 23, 2021
Personalized approach to childhood obesity: Lessons from gut microbiota and omics studies. Narrative review and insights from the 29th European childhood obesity congressAneta Gawlik, Anne Salonen, Ching Jian, et al.ACS Nano|July 12, 2018
Solvent- and Wavelength-Dependent Photoluminescence Relaxation Dynamics of Carbon Nanotube sp3 Defect StatesXiaowei He, Kirill A Velizhanin, George Bullard, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|November 12, 2020
Late diagnosis of 3β-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the HSD3B2 genePavlos Fanis, Vassos Neocleous, Konstantina Kosta, et al.Scientific Reports|August 4, 2026
Exonisation of an Alu element in the 3'-UTR contributes to SRD5A2 deficiencyRalf Werner, Anna Basina, Axel Künstner, et al.Pageof 80