Browse All

Current Filters

CLEAR FILTER x

TITLE

Outstripping of Motor Unit Compensation with Disease Severity in Adults with Spinal Muscular Atrophy

Author:Deardorff, Adam   Guerra Castanon, Felix   Zhao, Songzhu   Kelly, Kristina   Tellez, Marco   Heintzman, Sarah   Kolb, Stephen   Arnold, William   Elsheikh, Bakri   

Session Name:P3: Neuromuscular Disease: ALS, SMA, and Other Motor Neuron Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.009  

Author Institution:The Ohio State University Wexner Medical Center, Columbus, OH  The Ohio State University Wexner Medical Center, Columbus, UT  University of Missouri, columbia, MO  

Impact of Nusinersen treatment on quality of life in adult patients with Spinal Muscular Atrophy

Author:Guerra Castanon, Felix   Deardorff, Adam   Zhao, Songzhu   Severyn, Steven   Kelly, Kristrina   Tellez, Marco   Heintzman, Sarah   Sterling, Gary   Kolb, Stephen   Arnold, David   Elsheikh, Bakri   

Session Name:P3: Neuromuscular Disease: ALS, SMA, and Other Motor Neuron Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.010  

Author Institution:Ohio State University, Columbus, OH  University of Missouri, Missouri, MO  

VRK1 mutation associated with adult-onset spinal muscular atrophy and persistently elevated creatine kinase

Author:Rodriguez-Hernandez, Adrian   Carranza-Renteria, Octavio   Faktorovich, Svetlana   

Session Name:P3: Neuromuscular Disease: ALS, SMA, and Other Motor Neuron Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.011  

Author Institution:Charles E. Schmidt School of Medicine, Florida Atlantic University, Boca Raton, FL  Marcus Neuroscience Institute, Boca Raton, FL  

Mills’ Disease Variant

Author:Moussallem, Rasha   Jawdat, Omar   Jabari, Duaa   Pasnoor, Mamatha   Dimachkie, Mazen   Statland, Jeffery   

Session Name:P3: Neuromuscular Disease: ALS, SMA, and Other Motor Neuron Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.012  

Author Institution:University of Kansas Medical Center, Kansas City, KS  The University of Kansas Medical Center, Kansas City, KS  

A Rare Case of Hereditary Spastic Paraplegia 46 With Novel Compound Heterozygous GBA2 gene variants

Author:Gill, Sandeep   Gill, Sukhraj   Williamson, Madeline   Avila, J. David   

Session Name:P3: Neuromuscular Disease: ALS, SMA, and Other Motor Neuron Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.013  

Author Institution:Geisinger Medical Center , Bloomsburg, PA  Geisinger Medical Center , Bloomsberg, PA  Geisinger, Danville, PA  Geisinger Medical Center, Danville, PA