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Skeletal Radiology|February 8, 2011
MRI findings of neutrophilic fasciitis in a patient with acute febrile neutrophilic dermatosis (Sweet's syndrome)Michele Gaeta, Achille Mileto, Olimpia Musumeci, et al.Neuromuscular Disorders : NMD|August 28, 2012
Stiffness as a presenting symptom of an odd clinical condition caused by multiple sclerosis and myotonia congenitaSimona Portaro, Olimpia Musumeci, Vincenzo Rizzo, et al.Journal of Clinical Neuromuscular Disease|November 22, 2021
Methotrexate as a Steroid-Sparing Agent in Myasthenia Gravis: A Preliminary Retrospective StudyCarmelo Rodolico, Carmen Bonanno, Teresa Brizzi, et al.Neuromuscular Disorders : NMD|September 28, 2015
Clinical and pathophysiological clues of respiratory dysfunction in late-onset Pompe disease: New insights from a comparative study by MRI and respiratory function assessmentMichele Gaeta, Olimpia Musumeci, Stefania Mondello, et al.Molecular Genetics and Metabolism|August 7, 2013
Late-onset Pompe disease (LOPD): correlations between respiratory muscles CT and MRI features and pulmonary functionMichele Gaeta, Emanuele Barca, Paolo Ruggeri, et al.Frontiers in Neurology|March 21, 2022
Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic AspectsAntonino Lupica, Rosaria Oteri, Sara Volta, et al.Journal of Neurology|March 6, 2025
Cerebral foreign body reaction (CFBR) after endovascular treatments is a rare event to be aware of: case series and review of literatureGiorgia Atanasio, Salvatore Bertino, Mariano Velo, et al.Neuromuscular Disorders : NMD|October 26, 2002
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish familiesGeorgios M Hadjigeorgiou, Menachem Sadeh, Olimpia Musumeci, et al.Journal of Inherited Metabolic Disease|February 3, 2016
Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD)Federica Montagnese, Francesca Granata, Olimpia Musumeci, et al.Pageof 12