Browse All

Current Filters

CLEAR FILTER x

TITLE

Program Number:

Homozygous and Compound Heterozygous Mutations in the CLCN1 Gene Causes Myotonia in Two Related Saudi Families

Author:Pagliarani, Serena   Alabdulwahed, Alwaleed   Monfrini, Edoardo   Lucchiari, Sabrina   Comi, Giacomo   Di Fonzo, Alessio   AlAhmari, Aawadh   Abulaban, Ahmed   AlEyaid, Wafaa   

Session Name:P2: Neuromuscular and Clinical Neurophysiology (EMG): Genetic Myopathies  

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P2.032  

Author Institution:Department of Neurology, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia, Riyadh, Saudi Arabia  

Medication Reduction After Bilateral Globus Pallidus Internus Deep Brain Stimulation

Author:Lee, Philip   He, Xin   Patrie, James   Shaikh, Sajid Hameed   Higinbotham, Alissa   Dalrymple, William   Shah, Binit   Figari-Jordan, Renzo   

Session Name:P2: Movement Disorders: Neuromodulation: Patient Selection, Programming, and Outcomes 1  

Topic:Movement Disorders  

Program Number:P2.032  

Author Institution:University of Virginia, Charlottesville, VA  Aga Khan University, Karachi, Pakistan