Prodromal Huntington Disease as a Model for Functional Compensation of Early Neurodegeneration

Por Malejko, Kathrin, Weydt, Patrick, Süßmuth, Sigurd D., Grön, Georg, Landwehrmeyer, Bernhard G., Abler, Birgit
Publicado no PLoS One (2014)

Validation of a Prognostic Index for Huntington's Disease

Por Long, Jeffrey D., Langbehn, Douglas R., Tabrizi, Sarah J., Landwehrmeyer, Bernhard G., Paulsen, Jane S., Warner, John, Sampiao, Cristina
Publicado no Mov Disord (2016)

Summary of cerebrospinal fluid routine parameters in neurodegenerative diseases

Por Jesse, Sarah, Brettschneider, Johannes, Süssmuth, Sigurd D., Landwehrmeyer, Bernhard G., von Arnim, Christine A. F., Ludolph, Albert C., Tumani, Hayrettin, Otto, Markus
Publicado em 2010

Development of an ELISA assay for the quantification of soluble huntingtin in human blood cells

Por Massai, Luisa, Petricca, Lara, Magnoni, Letizia, Rovetini, Luca, Haider, Salman, Andre, Ralph, Tabrizi, Sarah J, Süssmuth, Sigurd D, Landwehrmeyer, Bernhard G, Caricasole, Andrea, Pollio, Giuseppe, Bernocco, Simonetta
Publicado no BMC Biochem (2013)

Disease Severity and Progression in Progressive Supranuclear Palsy and Multiple System Atrophy: Validation of the NNIPPS – PARKINSON PLUS SCALE

Por Payan, Christine A. M., Viallet, François, Landwehrmeyer, Bernhard G., Bonnet, Anne-Marie, Borg, Michel, Durif, Franck, Lacomblez, Lucette, Bloch, Frédéric, Verny, Marc, Fermanian, Jacques, Agid, Yves, Ludolph, Albert C., Leigh, Peter N., Bensimon, Gilbert
Publicado em 2011

Genetic Variants of the α-Synuclein Gene SNCA Are Associated with Multiple System Atrophy

Por Al-Chalabi, Ammar, Dürr, Alexandra, Wood, Nicholas W., Parkinson, Michael H., Camuzat, Agnes, Hulot, Jean-Sébastien, Morrison, Karen E., Renton, Alan, Sussmuth, Sigurd D., Landwehrmeyer, Bernhard G., Ludolph, Albert, Agid, Yves, Brice, Alexis, Leigh, P. Nigel, Bensimon, Gilbert
Publicado em 2009