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Sporadic Late Onset Nemaline Myopathy Presenting with Cranial Mononeuropathies

Author:Shammas, Ibrahim   Feher, Samuel   Granger, Andre   Kourelis, Taxiarchis   Naddaf, Elie   

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

Topic:Neuromuscular and Clinical Neurophysiology (EMG)  

Program Number:P3.019  

Author Institution:Mayo Clinic, MN, Rochester, MN  Mayo Clinic, FL, Jacksonville, FL  Mayo Clinic, MN, Rochester , MN  

Unique Presentation of Inflammatory Cerebral Amyloid Angiopathy (iCAA) Presenting as Acute Encephalopathy

Author:Khosa, Shaweta   Khosa, Gurveer   Anandaram, Sanjay   

Session Name:P3: Autoimmune Neurology: Paraneoplastic Neurological Disease and Other Inflammatory Disorders  

Topic:Autoimmune Neurology  

Program Number:P3.019  

Author Institution:Olive View-UCLA Medical Center, Granada Hills, CA  Adesh Institute of Medical Sciences & Research, Malout, India  Neuroscience Institute - Rochester General Hospital, Rochester, NY  

Spanish Language Adaptation of the ALLFTD Genetic Counseling Protocol in Costa Rica

Author:Josephy, Sylvia   Godoy, Maria Eugenia   Ibanez, Agustin   Boxer, Adam   Rosen, Howard   Forsberg, Leah   Heuer, Hilary   Boeve, Bradley   Leon Salas, Jorge Mario   

Session Name:P3: Aging, Dementia, and Behavioral Neurology: Genetics of Cognitive Disorders and Dementia  

Topic:Aging, Dementia, and Behavioral Neurology  

Program Number:P3.019  

Author Institution:Caja Costarricense de Seguro Social, San Jose, Costa Rica  Universidad Adolfo Ibáñez, Latin American Brain Health Institute, Buenos Aires, Chile  University of California, San Francisco, San Francisco, CA  UCSF, San Francisco, CA  Mayo Clinic, Rochester, MN  

PINK1 Parkinson’s Disease in New Zealand: An Overview

Author:Donnelly, Joseph   Buchanan, Christina   Patel, Shilpan   Vailahi, Garcia   Viali, Satupaitea   Puli’uvea, Chris   Dayal, Viswas   Roxburgh, Richard   

Session Name:P3: Movement Disorders: Parkinson's Disease Genetics, Biomarkers, and Basic Science  

Topic:Movement Disorders  

Program Number:P3.019  

Author Institution:Auckland City Hospital, Auckland, New Zealand  Auckland Hospital, Auckland, New Zealand  

The road towards implementation of TMEM106B genetic testing in clinical practice in progranulin pathogenic variant carriers

Author:Vandebergh, Marijne   Ramos, Eliana Marisa   Geschwind, Daniel   Mirza, Saira   Masellis, Mario   Rogaeva, Ekaterina   Chisman-Russell, Lucy   Rohrer, Jonathan   Heuer, Hilary   Forsberg, Leah   Boxer, Adam   Rosen, Howard   Boeve, Bradley   Rademakers, Rosa   

Session Name:P3: Aging, Dementia, and Behavioral Neurology: Genetics of Cognitive Disorders and Dementia  

Topic:Aging, Dementia, and Behavioral Neurology  

Program Number:P3.020  

Author Institution:University of Antwerp, Antwerp, Belgium, Antwerp, Belgium  University of California, Los Angeles, USA, Los Angeles, CA  Sunnybrook Health Sciences Centre and the University of Toronto, Toronto, Canada, Toronto, ON, Canada  San Francisco Weill Institute for Neurosciences, San Francisco, USA, San Francisco, CA  Mayo Clinic, Rochester, USA, Rochester, MN  Mayo Clinic, Jacksonville, USA, Antwerp, Belgium