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Journal of Neurology
|
January 9, 2019
A systematic review on the definition of rhabdomyolysis
Kristina Stahl, Emanuele Rastelli, Benedikt Schoser
Muscle & Nerve
|
December 2, 2017
Aquaporin 4 expression in human skeletal muscle fiber types
Elisa Vizzaccaro, Chiara Terracciano, Emanuele Rastelli, et al.
Current Opinion in Neurology
|
July 27, 2018
Towards clinical outcome measures in myotonic dystrophy type 2: a systematic review
Emanuele Rastelli, Federica Montagnese, Roberto Massa, et al.
Neuromuscular Disorders : NMD
|
September 5, 2020
How to capture activities of daily living in myotonic dystrophy type 2?
Federica Montagnese, Emanuele Rastelli, Kristina Stahl, et al.
Frontiers in Neurology
|
May 7, 2020
Validation of Motor Outcome Measures in Myotonic Dystrophy Type 2
Federica Montagnese, Emanuele Rastelli, Nina Khizanishvili, et al.
Ultrastructural Pathology
|
March 28, 2018
Neurofibromatous neuropathy: An ultrastructural study
Chiara Terracciano, Christa Pachatz, Emanuele Rastelli, et al.
Current Neurology and Neuroscience Reports
|
November 2, 2018
Comparative Sleep Disturbances in Myotonic Dystrophy Types 1 and 2
Andrea Romigi, Valentina Franco, Fabio Placidi, et al.
Muscle & Nerve
|
November 25, 2015
Neutral lipid-storage disease with myopathy and extended phenotype with novel PNPLA2 mutation
Roberto Massa, Simone Pozzessere, Emanuele Rastelli, et al.
Neuromuscular Disorders : NMD
|
October 2, 2018
Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1
Claudia Cutellè, Emanuele Rastelli, Manuela Gibellini, et al.
Neurophysiologie Clinique = Clinical Neurophysiology
|
June 30, 2020
Understanding hyper-reflexia in acute motor axonal neuropathy (AMAN)
Viviana Versace, Stefania Campostrini, Emanuele Rastelli, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Journal of Neurology
|
January 9, 2019
A systematic review on the definition of rhabdomyolysis
Kristina Stahl, Emanuele Rastelli, Benedikt Schoser
Muscle & Nerve
|
December 2, 2017
Aquaporin 4 expression in human skeletal muscle fiber types
Elisa Vizzaccaro, Chiara Terracciano, Emanuele Rastelli, et al.
Current Opinion in Neurology
|
July 27, 2018
Towards clinical outcome measures in myotonic dystrophy type 2: a systematic review
Emanuele Rastelli, Federica Montagnese, Roberto Massa, et al.
Neuromuscular Disorders : NMD
|
September 5, 2020
How to capture activities of daily living in myotonic dystrophy type 2?
Federica Montagnese, Emanuele Rastelli, Kristina Stahl, et al.
Frontiers in Neurology
|
May 7, 2020
Validation of Motor Outcome Measures in Myotonic Dystrophy Type 2
Federica Montagnese, Emanuele Rastelli, Nina Khizanishvili, et al.
Ultrastructural Pathology
|
March 28, 2018
Neurofibromatous neuropathy: An ultrastructural study
Chiara Terracciano, Christa Pachatz, Emanuele Rastelli, et al.
Current Neurology and Neuroscience Reports
|
November 2, 2018
Comparative Sleep Disturbances in Myotonic Dystrophy Types 1 and 2
Andrea Romigi, Valentina Franco, Fabio Placidi, et al.
Muscle & Nerve
|
November 25, 2015
Neutral lipid-storage disease with myopathy and extended phenotype with novel PNPLA2 mutation
Roberto Massa, Simone Pozzessere, Emanuele Rastelli, et al.
Neuromuscular Disorders : NMD
|
October 2, 2018
Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1
Claudia Cutellè, Emanuele Rastelli, Manuela Gibellini, et al.
Neurophysiologie Clinique = Clinical Neurophysiology
|
June 30, 2020
Understanding hyper-reflexia in acute motor axonal neuropathy (AMAN)
Viviana Versace, Stefania Campostrini, Emanuele Rastelli, et al.
Page
of 2