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Movement Disorders Associated with Cerebral Artery Stenosis: A Nationwide Study

Author:Chung, Sun Ju   Choi, Nari   Oh, Eungseok   Ryu, Ho-Sung   You, Sooyeoun   Kim, Bum Joon   Lee, Seung Hyun   Park, Kye Won   

Session Name:P13: Movement Disorders: Miscellaneous Movement Disorders 1  

Topic:Movement Disorders  

Program Number:P13.003  

Author Institution:Neurology, Asan Medical Center, Seoul, Korea, Republic of  Heavenly Hospital, Goyang, Korea, Republic of  Chungnam National University College of Medicine, Daejeon, Korea, Republic of  Kyungpook National University Hospital, Daegu, Korea, Republic of  Dongsan Medical Center, Daegu, Korea, Republic of  Asan Medical Center, Seoul, Korea, Republic of  Seoul Medical Center, Seoul, Korea, Republic of  Uijeongbu Eulji University Hospital, Uijoengbu-si, Korea, Republic of  

Use of Liver Transplantation for Pure Neurologic Indications in Wilson Disease

Author:Marmol, Sarah   Feldman, Matthew   hislop, jenna   Shpiner, Danielle   Margolesky, Jason   

Session Name:P13: Movement Disorders: Miscellaneous Movement Disorders 1  

Topic:Movement Disorders  

Program Number:P13.004  

Author Institution:University of Miami, Miami, FL  Movement Disorders Fellowship - University of Miami, MIAMI, FL  Miami VAMC, Miami, FL  University of Miami Miller School of Medicine, Miami, FL  University of Miami School of Medicine, Miami, FL  

The Clinical And Molecular Spectrum Of ZFYVE26-Associated Hereditary Spastic Paraplegia (SPG15)

Author:Saffari, Afshin   Jordan, Catherine   Mo, Alisa   Zhang, Bo   Sahin, Mustafa   Blackstone, Craig   Yang, Edward   Ebrahimi-Fakhari, Darius   

Session Name:P13: Movement Disorders: Miscellaneous Movement Disorders 1  

Topic:Movement Disorders  

Program Number:P13.005  

Author Institution:Boston Children's Hospital, Boston, MA  Massachusetts General Hospital, Charlestown, MA  Boston Children's Hospital, Jamaica Plain, MA  Boston Children's Hospital, Brookline, MA  

Late-onset POLR3-related Leukodystrophy: report of a novel compound heterozygous mutation in the POLR3A gene and review of the phenotype

Author:Pesantez Pacheco, Laura   Hallett, Mark   

Session Name:P13: Movement Disorders: Miscellaneous Movement Disorders 1  

Topic:Movement Disorders  

Program Number:P13.006  

Author Institution:National Institute of Neurological Disorders and Stroke, Bethesda, MD  National Institutes of Health, Bethesda, MD  

Caspr2 Antibody-Mediated Ataxia, Parkinsonism, and Epilepsy: A Case for Escalating Immunotherapy.

Author:Sugar, Dana   Witek, Natalie   

Session Name:P13: Movement Disorders: Miscellaneous Movement Disorders 1  

Topic:Movement Disorders  

Program Number:P13.007  

Author Institution:Rush University, Chicago, IL