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A Tale of Two Brothers: Two Cases of Symptomatic Heterozygous HTRA1 Mutations

Author:Sacks, Benjamin   Athwal, Bal   

Session Name:P8: Cerebrovascular Disease and Interventional Neurology: Neurovascular Conditions and Rare Strokes Etiologies 2  

Topic:Cerebrovascular Disease and Interventional Neurology  

Program Number:P8.014  

Author Institution:Royal Free Hospital London NHS Foundation Trust, London, UK, NW3 2QG, United Kingdom  

Natural History of Gerstmann-Sträussler-Scheinker Syndrome in a Brazilian Cohort

Author:Oliveira Marques, Marcos Vinicius   Silva, Thiago   Pedroso, Jose Luiz   Barsottini, Orlando   Zanoteli, Edmar   

Session Name:P8: Movement Disorders: Rare Movement Disorders  

Topic:Movement Disorders  

Program Number:P8.014  

Author Institution:Saint Louis University , Saint Louis, MO  Unifesp, São Paulo, Brazil  Universidade Federal De Sao Paulo, Sao Paulo, Brazil  Universidade Federal de São Paulo, Sao Paulo- SP, Brazil  University of São Paulo, Sao Paulo, Brazil  

Presentation of Various Neurological Symptoms Alongside Heerfordt’s Syndrome Leads to the Diagnosis of Sarcoidosis.

Author:Canenguez, Johanna   Lerint, Alexandru   Morakinyo, Oreoluwa   Komal, Fnu   

Session Name:P8: Autoimmune Neurology: Immune Therapy Complications, Neurorheumatology, and Other Inflammatory Disorders  

Topic:Autoimmune Neurology  

Program Number:P8.014  

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