Showing results (531-540 of 543) with videos related to

Sort By:
Pageof 55
Frontiers in Endocrinology|August 22, 2022
Corrigendum: The silent epidemic of diabetic ketoacidosis at diagnosis of type 1 diabetes in children and adolescents in italy during the covid-19 pandemic in 2020Valentino Cherubini, Monica Marino, Andrea E Scaramuzza, et al.
Frontiers in Endocrinology|July 5, 2022
The Silent Epidemic of Diabetic Ketoacidosis at Diagnosis of Type 1 Diabetes in Children and Adolescents in Italy During the COVID-19 Pandemic in 2020Valentino Cherubini, Monica Marino, Andrea E Scaramuzza, et al.
Clinical Chemistry and Laboratory Medicine|May 19, 2021
S100B protein, cerebral ultrasound and magnetic resonance imaging patterns in brain injured preterm infantsGiorgia Gasparroni, Alessandro Graziosi, Iliana Bersani, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for diabetes, obesity, and metabolismChantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
Hormone Research in Paediatrics|November 26, 2025
EndoCompass Project: Research Roadmap for Diabetes, Obesity, and MetabolismChantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
Pediatric Diabetes|November 22, 2017
Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomesTimothy C Skinner, Karin S Lange, Hilary Hoey, et al.
JAMA Pediatrics|April 13, 2026
Nirsevimab Immunization to Prevent Pediatric RSV HospitalizationsFederica Attaianese, Giulia Carreras, Sandra Trapani, et al.
Italian Journal of Pediatrics|August 2, 2018
Diagnosis, treatment and prevention of pediatric obesity: consensus position statement of the Italian Society for Pediatric Endocrinology and Diabetology and the Italian Society of PediatricsGiuliana Valerio, Claudio Maffeis, Giuseppe Saggese, et al.
Med (New York, N.Y.)|April 27, 2024
An international multidisciplinary consensus on pediatric metabolic dysfunction-associated fatty liver diseaseLe Zhang, Mortada El-Shabrawi, Louise A Baur, et al.
American Journal of Human Genetics|December 20, 2023
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndromeVincenzo Salpietro, Reza Maroofian, Maha S Zaki, et al.
Pageof 55