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Hereditary Myopathy with Early Respiratory Failure (HMERF): A Case Report and Review of the Literature

Author:Calisaya-Madariaga, Irving   Acurio, Karlos   Pacheco, Niels   Chuquilin Arista, Miguel   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Genetic Muscle Diseases  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.014  

Author Institution:Universidad Peruana Cayetano Heredia, Lima, Peru  Universidad Peruana Cayetano Heredia, Cusco, Peru  Harvard Medical School, Boston, MA  University of Florida, Gainesville, FL  

Late onset myopathy related to CACNA1S mutation: expanding the phenotype.

Author:Ahmed, Samreen   Mnatsakanova, Diana   Paul, Pritikanta   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Genetic Muscle Diseases  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.015  

Author Institution:University of Illinois in Chicago, Glen Ellyn, IL  University of Illinois in Chicago, Chicago, IL  University of California, San Francisco, San Francisco, CA  

Clinical Characteristics of Myotonic Dystrophy with Associated Parkinsonism: An 11 Patients Case Series

Author:Nascimento Andrade, Eduardo Inacio   Smith, kara   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Genetic Muscle Diseases  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.016  

Author Institution:University of Massachusetts Chan Medical School, Worcester, MA  University Of Massachusetts Chan Medical School , Worcester, MA  

Adult-onset Leigh Syndrome: An analysis of the North American Mitochondrial Disease Consortium Database

Author:Barca, Emanuele   Kroopnick, Adam   Houck, Alexander   Thakur, Kiran   Dugue, Rachelle   Zolkipli-Cunningham, Zarazuela   Falk, Marni   Goldstein, Amy   Demczko, Matthew   Gavrilova, Ralitza   Larson, Austin   Van Hove, Johan   Saneto, Russell   Buchsbaum, Richard   Thompson, John   Hirano, Michio   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Genetic Muscle Diseases  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.017  

Author Institution:Columbia University Irving Medical Center, New York, NY  Stanford University, Palo Alto, CA  The Children's Hospital of Philadelphia, Philadelphia, PA  Mayo Clinic, Rochester, MN  Children`s Hospital Colorado, Aurora, CO  Seattle Childrens Hospital, Seattle, WA  Columbia Univ School of Public Health, New York, NY  

Lipid Metabolism Myopathy Associated with Predominantly Chronic Motor Neuron Disorder

Author:Mauney, Sarah   El Seblani, Nader   Su, Xiaowei   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Genetic Muscle Diseases  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.018  

Author Institution:Penn State Milton S. Hershey Medical Center, Hershey, PA  Penn State Health Milton S. Hershey Medical Center, Hershey, PA