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Fasciculations Secondary to Severe Vitamin B12 Deficiency Mimicking Motor Neuron Disease

Author:Kaur, Manmeet   Morakinyo, Oreoluwa   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Case Studies in Neuromuscular Medicine 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:Neuromuscular and Clinical Neurophysiology (EMG)  

Author Institution:University of Texas Medical Branch, Galveston TX, Galveston, TX  

Recognizing Amyotrophic Lateral Sclerosis Early: Bilateral Internal Capsule Hyperintensities as a Diagnostic Clue

Author:Shahrigian, Taleen   Schick, Jason   Gilbert, Christopher   Antonio, Aileen   Goshgarian, Christopher   Taylor, Melanie   Phillips, Joel   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Case Studies in Neuromuscular Medicine 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:Neuromuscular and Clinical Neurophysiology (EMG)  

Author Institution:Trinity Health Grand Rapids, Grand Rapids, MI  Trinity Health Saint Mary's Hauenstein Neurosciences, Grand Rapids, MI  Trinity Health Grand Rapids , Ada, MI  Trinity Health Grand Rapids , Grand Rapids, MI  

Mitochondrial Trifunctional Protein Deficiency Masquerading as Charcot-Marie-Tooth Disease

Author:Cakar, Arman   Mus, Bilgehan   Durmus, Hacer   Parman, Fatma Yesim   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Case Studies in Neuromuscular Medicine 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:Neuromuscular and Clinical Neurophysiology (EMG)  

Author Institution:Neuromuscular Unit, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey  Neuromuscular Unit, Istanbul University, Istanbul Faculty of Medicine, Turkey  

A PNPLA6 Variant Case Report With a Combination of Heterozygous Mutations

Author:Blackbourn, Lisle   Chai, Eric   Zallek, Christopher   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Case Studies in Neuromuscular Medicine 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:Neuromuscular and Clinical Neurophysiology (EMG)  

Author Institution:University of Illinois College of Medicine Peoria, Elkhorn, WI  University of Illinois College of Medicine Peoria, IL  University of Illinois College of Medicine Peoria, Peoria Heights, IL  

Rare Case of Hereditary Transthyretin Amyloidosis With a Val122Ile Mutation Presenting as Recurrent Foot Drop in a Young Woman

Author:Khan, Imran   Malik, Hanna   LaBoy, Shannon   

Session Name:P3: Neuromuscular and Clinical Neurophysiology (EMG): Case Studies in Neuromuscular Medicine 2  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:Neuromuscular and Clinical Neurophysiology (EMG)  

Author Institution:University of Florida Jacksonville, FL  UF Health Neurology, Jacksonville, FL