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A Phase 2/3 Adaptive Design Study of GHF-201 as the First Potential Treatment of Adult Polyglucosan Body Disease

Author:Hirano, Michio   Weil, Miguel   Kakhlon, Or   Mordechai, Anat   Garti, Nissim   Gilgun-Sherki, Yossi   Lossos, Alexander   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:Neuromuscular and Clinical Neurophysiology (EMG)  

Author Institution:Columbia University Medical Center, New York, NY  Tel-Aviv University, Tel Aviv, Israel  Hadassah Hospital, Jerusalem, Israel  Lyotropic Delivery Systems Ltd, Jerusalem, Israel  Golden Heart Flower, Afula, Israel  

Late-onset Tay-Sachs Disease Mimicking Amyotrophic Lateral Sclerosis: A Report of Three Cases

Author:Cantu-Martinez, Leonel   Martinez, Hector   Figueroa Sanchez, Jose A   Gutierrez Trevino, Oscar   Gamez Lopez, Sebastian   Perez Martinez, Beatriz   Pons Monnier, Guillermo   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:Neuromuscular and Clinical Neurophysiology (EMG)  

Author Institution:Instituto de Neurologia y Neurocirugia, Centro Medico Zambrano Hellion, TecSalud, San Pedro NL, Mexico  Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Monterrey, Mexico  

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:Neuromuscular and Clinical Neurophysiology (EMG)  

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:Neuromuscular and Clinical Neurophysiology (EMG)  

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:Neuromuscular and Clinical Neurophysiology (EMG)  

Author Institution:Rush University Medical Center, Chicago, IL