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Genotype-Phenotype correlation in Parkin-Parkinson’s disease

Author:Jayadev Menon, Poornima   Sambin, Sara   Criniere-Boizet, Baptiste   Courtin, Thomas   Casse, Fanny   Tesson, Christelle   Ferrien, Melanie   Flamand-Roze, Emmanuel   Lejeune, Francois-Xavier   Lanore, Aymeric   Mangone, Graziella   Mariani, Louise-Laure   Aasly, Jan   Gan Or, Ziv   Yu, Eric   Dauvilliers, Yves   Zimprich, Alexander   Alvarez Fernandez, Ignacio   Pastor, Pau   Di Fonzo, Alessio   Bhatia, Khailash   Magrinelli, Francesca   Houlden, Henry   Real, Raquel   Narendra, Derek   Lin, Hsin-Pin   Jovanovic, Carna   Koks, Sulev   Lynch, Timothy   Gallagher, Amy   Vandenberghe, Wim   Gasser, Thomas   Morris, Huw   Klein, Christine   Brockmann, Kathrin   Corti, Olga   Brice, Alexis   Lesage, Suzanne   Corvol, Jean-Christophe   

Session Name:P3: Movement Disorders: Biomarkers and Genetics of Parkinson's Disease 1  

Topic:Movement Disorders  

Program Number:P3.012  

Author Institution:ICM/ Paris Brain Institute, Paris, France  NTNU, Trondheim, Norway  Mcgill University, Montreal, QC, Canada  Montpellier, Montpellier, France  Medizinische Universität Wien, Vienna, Austria  University Mutua de Terrassa, Terrassa, Spain  University of Milan, Milan, Italy  UCL, London, United Kingdom  NIH, Bethesda, MD  University of Belgrade, Belgrade, Serbia  University of Perron, Perth, Australia  Dublin Neurological Institute, Dublin, Ireland  University of Leuven, Leuven, Belgium  University of Tuebingen, Tuebingen, Germany  University of Luebeck, Luebeck, Germany  

Evaluation of methodologies for indirect comparison of eplontersen and vutrisiran for the treatment of hereditary transthyretin-mediated amyloidosis with polyneuropathy