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Seminars in Fetal & Neonatal Medicine|June 10, 2011
Mitochondrial DNA mutations and depletion in pediatric medicineA SpinazzolaJournal of Internal Medicine|February 5, 2009
Disorders from perturbations of nuclear-mitochondrial intergenomic cross-talkA Spinazzola, M ZevianiScience (New York, N.Y.)|January 29, 1999
Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorderI Nishino, A Spinazzola, M HiranoNeuromuscular Disorders : NMD|February 13, 2001
MNGIE: from nuclear DNA to mitochondrial DNAI Nishino, A Spinazzola, M HiranoJournal of Ultrasound|February 12, 2013
Ultrasound guided treatment of pseudoaneurysm caused by puncture of the common femoral arteryA Spinazzola, L Cireni, A FarinaJournal of Ultrasound|February 12, 2013
Diagnosis and treatment of abdominal aortic endoleaks using color Doppler US: Two clinical casesG Nano, S Stegher, A SpinazzolaThe Annals of Thoracic Surgery|January 1, 1979
Axillofemoral bypass: intrapleural methodV Tangpraphaphorn, A Spinazzola, J KingAnnali Dell'Istituto Superiore Di Sanita|January 1, 1977
[Environmental dust in a plant for the production of polyvinyl chloride]D Casula, P Cherchi, G Spiga, et al.Nucleosides, Nucleotides & Nucleic Acids|December 2, 2004
Thymidine phosphorylase deficiency causes MNGIE: an autosomal recessive mitochondrial disorderM Hirano, R Martí, A Spinazzola, et al.Giornale Italiano Di Medicina Del Lavoro|July 1, 1982
[The work environment in steel-cord production]S Atzeri, P Bario, P Cherchi, et al.Pageof 3