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Journal of Clinical Research in Pediatric Endocrinology|November 21, 2012
Thyroid nodules in pediatrics: which ones can be left alone, which ones must be investigated, when and howAndrea Corrias, Alessandro MussaCancers|October 28, 2023
Introduction to the Beckwith-Wiedemann Syndrome and Cancer Special IssueAlessandro Mussa, Jennifer M KalishEuropean Journal of Emergency Medicine : Official Journal of the European Society for Emergency Medicine|November 9, 2005
A case of severe hypercalcemia with acute renal failure in sarcoidosis: a diagnostic challenge for the emergency departmentGiovanni Volpicelli, Alessandro Mussa, Mauro FrasciscoJournal of Clinical Ultrasound : JCU|September 13, 2012
Sonographic diagnosis of pulmonary embolism with cardiac arrest without major dilation of the right ventricle or direct sign of lower limb venous thrombosisGiovanni Volpicelli, Alessandro Mussa, Mauro F FrasciscoUltrasound in Medicine & Biology|March 4, 2008
Phalangeal quantitative ultrasound in children with phenylketonuria: a pilot studyFrancesco Porta, Marco Spada, Roberto Lala, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2024
Cognitive, Social, and Emotional-Behavioral Outcomes in Children and Adolescents With Beckwith-Wiedemann SyndromeNiccolò Butti, Cosimo Urgesi, Alessandro Mussa, et al.Journal of Clinical Research in Pediatric Endocrinology|April 11, 2019
Syndromic Disorders Caused by Disturbed Human ImprintingDiana Carli, Evelise Riberi, Giovanni Battista Ferrero, et al.Molecular Genetics and Metabolism|February 14, 2012
Dopamine agonists in dihydropteridine reductase deficiencyFrancesco Porta, Alessandro Mussa, Daniela Concolino, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2006
Image diagnosis in McCune-Albright syndromeClaudio Defilippi, Domenico Chiappetta, Daniela Marzari, et al.International Journal of Environmental Research and Public Health|February 25, 2022
Maxillo-Facial Morphology in Beckwith-Wiedemann Syndrome: A Preliminary Study on (epi)Genotype-Phenotype Association in CaucasiansPatrizia Defabianis, Alessandro Mussa, Rossella Ninivaggi, et al.Pageof 16