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Giuliano Tomelleri

Showing results (1-10 of 55) with videos related to

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Current Opinion in Rheumatology|August 25, 2012
Critical illness myopathyNicola Latronico, Giuliano Tomelleri, Massimiliano Filosto
Journal of Clinical Pathology|August 3, 2019
Relapsing-remitting painful masses of the skeletal muscleGaetano Vattemi, Valeria Guglielmi, Matteo Marini, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: A case report with 25 years of follow-upMauro Scarpelli, Giuliano Tomelleri, Laura Bertolasi, et al.
Genetics Research International|May 9, 2012
Mitochondrial Sensorineural Hearing Loss: A Retrospective Study and a Description of Cochlear Implantation in a MELAS PatientMauro Scarpelli, Francesca Zappini, Massimiliano Filosto, et al.
Acta Neuropathologica|March 22, 2002
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseasesMassimiliano Filosto, Paola Tonin, Gaetano Vattemi, et al.
Electrophoresis|September 19, 2015
Immunoblot as a potential diagnostic tool for myofibrillar myopathiesMatteo Marini, Valeria Guglielmi, Georgine Faulkner, et al.
Journal of Neuropathology and Experimental Neurology|September 15, 2018
Acute Sarcomeric M-Line Disease Associated With ATP Synthase Subunit α Autoantibodies in Ankylosing SpondylitisValeria Guglielmi, Gaetano Vattemi, Daniela Cecconi, et al.
Rheumatology International|January 15, 2008
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality?Sara Simeoni, Antonio Puccetti, Elisa Tinazzi, et al.
Journal of the Neurological Sciences|August 19, 2014
Polymyositis in solid organ transplant recipients receiving tacrolimusGaetano Vattemi, Matteo Marini, Marzia Di Chio, et al.
Neuromuscular Disorders : NMD|September 29, 2009
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M genePaola Tonin, Claudio Bruno, Denise Cassandrini, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Current Opinion in Rheumatology|August 25, 2012
Critical illness myopathyNicola Latronico, Giuliano Tomelleri, Massimiliano Filosto
Journal of Clinical Pathology|August 3, 2019
Relapsing-remitting painful masses of the skeletal muscleGaetano Vattemi, Valeria Guglielmi, Matteo Marini, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: A case report with 25 years of follow-upMauro Scarpelli, Giuliano Tomelleri, Laura Bertolasi, et al.
Genetics Research International|May 9, 2012
Mitochondrial Sensorineural Hearing Loss: A Retrospective Study and a Description of Cochlear Implantation in a MELAS PatientMauro Scarpelli, Francesca Zappini, Massimiliano Filosto, et al.
Acta Neuropathologica|March 22, 2002
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseasesMassimiliano Filosto, Paola Tonin, Gaetano Vattemi, et al.
Electrophoresis|September 19, 2015
Immunoblot as a potential diagnostic tool for myofibrillar myopathiesMatteo Marini, Valeria Guglielmi, Georgine Faulkner, et al.
Journal of Neuropathology and Experimental Neurology|September 15, 2018
Acute Sarcomeric M-Line Disease Associated With ATP Synthase Subunit α Autoantibodies in Ankylosing SpondylitisValeria Guglielmi, Gaetano Vattemi, Daniela Cecconi, et al.
Rheumatology International|January 15, 2008
Systemic sclerosis and superficial siderosis of the central nervous system: casuality or causality?Sara Simeoni, Antonio Puccetti, Elisa Tinazzi, et al.
Journal of the Neurological Sciences|August 19, 2014
Polymyositis in solid organ transplant recipients receiving tacrolimusGaetano Vattemi, Matteo Marini, Marzia Di Chio, et al.
Neuromuscular Disorders : NMD|September 29, 2009
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M genePaola Tonin, Claudio Bruno, Denise Cassandrini, et al.
Pageof 6