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Valosin-containing Protein-associated Myopathy: A Genetic Link Between Familial Amyotrophic Lateral Sclerosis and Inclusion Body Myositis

Author:Stearns, Hunter   Vanood, Aimen   Jacobi, Jackie   

Session Name:P5: Neuromuscular and Clinical Neurophysiology (EMG): Motor Neuron Disorders  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P5.016  

Author Institution:Mayo Clinic Arizona, Scottsdale, AZ  Mayo Clinic Arizona, AZ  

Novel Compound Heterozygous SPG7 Mutation Mimicking Amyotrophic Lateral Sclerosis

Author:Doward, Matthew   Granger, Andre   

Session Name:P5: Neuromuscular and Clinical Neurophysiology (EMG): Motor Neuron Disorders  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P5.017  

Author Institution:Mayo Clinic , FL  Mayo Clinic, Jacksonville, FL  

PSEN1 Mutation Presenting as Isolated Hereditary Spastic Paraplegia

Author:Joyce, Jessica   Dineen, Richard   Jacobson, Ryan   

Session Name:P5: Neuromuscular and Clinical Neurophysiology (EMG): Motor Neuron Disorders  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P5.018  

Author Institution:Rush University Medical Center, Chicago, IL  

Vigorous Physical Activity Accelerates ALS Symptom Onset in Sporadic and Genetic Cases

Author:Grassano, Maurizio   Tosetto, Federico   Moglia, Cristina   Calvo, Andrea   Chio, Adriano   

Session Name:P5: Neuromuscular and Clinical Neurophysiology (EMG): Motor Neuron Disorders  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P5.019  

Author Institution:ALS Center, Department of Neuroscience, University of Turin, Torino, Italy  

TDP-43 Cooperates With Nuclear Exosome Targeting Complex in Regulating SCARNA2 Metabolism

Author:Oshima, Yuki   Suzuki, Hidefumi   Abe, Ryota   Ogawa, Shintaro   Ike, Yoko   Yaguchi, Hiroaki   Takahashi, Hidehisa   Yabe, Ichiro   

Session Name:P5: Neuromuscular and Clinical Neurophysiology (EMG): Motor Neuron Disorders  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P5.020  

Author Institution:Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Yokohama-shi, Kanagawa, Japan  Department of Molecular Biology, Yokohama City University, Japan  Department of Neurology and Stroke Medicine, Yokohama City University , Japan  Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan