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Heart Failure Clinics|November 15, 2021
Genetics in Congenital Heart Diseases: Unraveling the Link Between Cardiac Morphogenesis, Heart Muscle Disease, and Electrical DisordersAnwar Baban, Valentina Lodato, Giovanni Parlapiano, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|March 31, 2012
Ebstein's anomaly in a child with osteogenesis imperfecta type IPatrizia D'Eufemia, Mauro Celli, Paolo Versacci, et al.
Pediatric Research|February 13, 2014
Serum brain-type creatine kinase increases in children with osteogenesis imperfecta during neridronate treatmentPatrizia D'Eufemia, Roberto Finocchiaro, Ciro Villani, et al.
Journal of Pediatric Orthopedics. Part B|April 1, 2014
Scoliosis secondary to ganglioneuroma: a case report and up to date literature reviewPatrizia D'Eufemia, Enrico Properzi, Marta Palombaro, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|January 5, 2013
Child abuse and osteogenesis imperfecta: how can they be still misdiagnosed? A case reportPatrizia D'Eufemia, Marta Palombaro, Valentina Lodato, et al.
Biomolecules|November 27, 2021
Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in ChildrenAnwar Baban, Valentina Lodato, Giovanni Parlapiano, et al.
Journal of Cardiovascular Development and Disease|November 25, 2021
1p36 Deletion Syndrome and the Aorta: A Report of Three New Patients and a Literature ReviewValentina Lodato, Valeria Orlando, Viola Alesi, et al.
Journal of Cardiovascular Development and Disease|October 26, 2022
Cardiovascular Involvement in Pediatric <i>FLNC</i> Variants: A Case Series of Fourteen PatientsAnwar Baban, Viola Alesi, Monia Magliozzi, et al.
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