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The Cochrane Database of Systematic Reviews|May 24, 2016
Salbutamol for transient tachypnea of the newbornLuca Moresco, Matteo Bruschettini, Amnon Cohen, et al.
American Journal of Medical Genetics|January 25, 2002
Meier-Gorlin syndrome (ear-patella-short stature syndrome) in an Italian patient: clinical evaluation and analysis of possible candidate genesAmnon Cohen, Roberta Mulas, Marco Seri, et al.
Nutrients|September 28, 2021
Early Pediatric Benefit of Lutein for Maturing Eyes and Brain-An OverviewDiego Gazzolo, Simonetta Picone, Alberto Gaiero, et al.
Italian Journal of Pediatrics|March 22, 2021
Management and outcome of benign acute childhood myositis in pediatric emergency departmentGiacomo Brisca, Marcello Mariani, Daniela Pirlo, et al.
Neurogenetics|January 31, 2014
A novel homozygous splicing mutation in PSAP gene causes metachromatic leukodystrophy in two Moroccan brothersLaura Siri, Andrea Rossi, Federica Lanza, et al.
American Journal of Medical Genetics. Part A|March 21, 2017
Maxillofacial features and systemic malformations in expanded spectrum Hemifacial MicrosomiaNoah Cohen, Erica Cohen, Alberto Gaiero, et al.
Pediatric Transplantation|May 23, 2006
Distinctive characteristics of diabetes mellitus after hematopoietic cell transplantation during childhoodSonia Bonanomi, Alberto Gaiero, Nicoletta Masera, et al.
Frontiers in Clinical Diabetes and Healthcare|March 30, 2023
Increased Frequency of Diabetic Ketoacidosis: The Link With COVID-19 PandemicGiuseppe d'Annunzio, Marta Bassi, Elena Lucia De Rose, et al.
Frontiers in Public Health|February 27, 2026
A region-wide hub and spoke approach to standardize and decentralize type 1 diabetes managementNicola Minuto, Giordano Spacco, Giulia Siri, et al.
Frontiers in Endocrinology|December 28, 2023
Pubertal attainment and Leydig cell function following pediatric hematopoietic stem cell transplantation: a three-decade longitudinal assessmentAlessandro Cattoni, Maria Laura Nicolosi, Giulia Capitoli, et al.
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