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Genetic panel testing's diagnostic accuracy for hereditary neuromuscular diseases in Hospital Universitário Antônio Pedro

Author:Adolphsson, Lorena   Braga, Carolina   Pupe, Camila   Eiras, Renata   Pinheiro, Thiago   Nascimento, Osvaldo   Azevedo, Helen   

Session Name:P1: Neuromuscular Disease: Imaging, Genetics and Outcome Measures  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P1.014  

Author Institution:UFF, Niteroi, Brazil  UFF, Rio De Janeiro, Brazil  UFF, Niterói, Brazil  Fluminense Federal University, Rio De Janeiro, Brazil  UFF, Rio de Janeiro , Brazil  

Validation of the Toronto Cramp Impact Index (TCII) for Assessment of Muscle Cramps

Author:Katzberg, Hans   Alnajjar, Sara   Alfaidi, Nouf   Mendoza, Meg   Zinman, Lorne   Abrahao, Agessandro   Shah, Hemant   Cherney, David   Bril, Vera   Barnett Tapia, Carolina   

Session Name:P1: Neuromuscular Disease: Imaging, Genetics and Outcome Measures  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P1.015  

Author Institution:University of Toronto, Toronto, ON, Canada  Sunnybrook Health Sciences Centre - University of Toronto, Toronto, ON, Canada  Toronto General Hospital, Toronto, ON, Canada  

Burden of Myasthenia Gravis Based on Sentiment Analysis of Patients’ Digital Conversations

Author:Brethenoux, Caroline   Pesa, Jacqueline   Chaudhry, Zia   Furey, Patrick   Gil Valleta, Lili   Gonzales Quijano, Laura   Lorenzo, Alex   

Session Name:P2: Neuromuscular Disease: Neuromuscular Junction Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.001  

Author Institution:CulturIntel, Irving, TX  Janssen Scientific Affairs, LLC, Superior, CO  Janssen Scientific Affairs, LLC, Titusville, NJ  CulturIntel, New York, NY  

The clinical and genetic characteristics of 17 cases with Congenital Myasthenic Syndrome: Data from a single center

Author:Yunisova, Gulshan   Arduç Akçay, Ayfer   Avci, Sahin   Eraslan, Serpil   Kayserili, Hülya   Oflazer, Piraye   

Session Name:P2: Neuromuscular Disease: Neuromuscular Junction Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.002  

Author Institution:Koç University Hospital, Muscle Center, Istanbul, Turkey  Koç University Hospital, Istanbul, Turkey  Koç University Hospital, Department of Medical Genetics & Genetic Diseases Evaluation Center, Istanbul, Turkey  Koç University , Istanbul, Turkey  

VAMP-1 associated congenital myasthenic syndrome: a demonstrative case with response to low-dose pyridostigmine

Author:Drakou, Eleni   Delfiner, Leslie   

Session Name:P2: Neuromuscular Disease: Neuromuscular Junction Disorders 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.003  

Author Institution:Montefiore Medical Center, Bronx, NY