Targeting Huntingtin Expression in Patients with Huntington’s Disease von Tabrizi, Sarah J, Leavitt, Blair R, Landwehrmeyer, G. Bernhard, Wild, Edward J, Saft, Carsten, Barker, Roger A, Blair, Nick F, Craufurd, David, Priller, Josef, Rickards, Hugh, Rosser, Anne, Kordasiewicz, Holly B, Czech, Christian, Swayze, Eric E, Norris, Daniel A, Baumann, Tiffany, Gerlach, Irene, Schobel, Scott A, Paz, Erika, Smith, Anne V, Bennett, C. Frank, Lane, Roger M

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Catatonia: looking back and moving forward von Hirjak, Dusan, Wolf, Robert Christian, Landwehrmeyer, G Bernhard, Northoff, Georg

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Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis von Tabrizi, Sarah J, Prof, Scahill, Rachael I, PhD, Durr, Alexandra, MD, Roos, Raymund AC, MD, Leavitt, Blair R, FRCPC, Jones, Rebecca, MSc, Landwehrmeyer, G Bernhard, MD, Fox, Nick C, MD, Johnson, Hans, PhD, Hicks, Stephen L, PhD, Kennard, Christopher, FRCP, Craufurd, David, FRCPsych, Frost, Chris, PhD, Langbehn, Douglas R, MD, Reilmann, Ralf, MD, Stout, Julie C, PhD

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Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): Standardized protocol and reference values von Rolke, R., Baron, R., Maier, C., Tölle, T.R., Treede, R.-D., Beyer, A., Binder, A., Birbaumer, N., Birklein, F., Bötefür, I.C., Braune, S., Flor, H., Huge, V., Klug, R., Landwehrmeyer, G.B., Magerl, W., Maihöfner, C., Rolko, C., Schaub, C., Scherens, A., Sprenger, T., Valet, M., Wasserka, B.

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Neuropsychiatric symptoms are very common in premanifest and early stage Huntington's Disease von Martinez-Horta, Saul, Perez-Perez, Jesus, van Duijn, Erik, Fernandez-Bobadilla, Ramon, Carceller, Mar, Pagonabarraga, Javier, Pascual-Sedano, Berta, Campolongo, Antonia, Ruiz-Idiago, Jesus, Sampedro, Frederic, Landwehrmeyer, G.Bernhard, Kulisevsky, Jaime

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Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): Somatosensory abnormalities in 1236 patients with different neuropathic pain syndromes von Maier, C., Baron, R., Tölle, T.R., Binder, A., Birbaumer, N., Birklein, F., Gierthmühlen, J., Flor, H., Geber, C., Huge, V., Krumova, E.K., Landwehrmeyer, G.B., Magerl, W., Maihöfner, C., Richter, H., Rolke, R., Scherens, A., Schwarz, A., Sommer, C., Tronnier, V., Üçeyler, N., Valet, M., Wasner, G., Treede, R.-D.

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Update on Huntington's disease: Advances in care and emerging therapeutic options von Zielonka, Daniel, Mielcarek, Michal, Landwehrmeyer, G. Bernhard

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Tominersen in Adults with Manifest Huntington's Disease von McColgan, Peter, Thobhani, Alpa, Boak, Lauren, Schobel, Scott A, Nicotra, Alessia, Palermo, Giuseppe, Trundell, Dylan, Zhou, Julian, Schlegel, Valerie, Sanwald Ducray, Patricia, Hawellek, David J, Dorn, Jonas, Simillion, Cedric, Lindemann, Michael, Wheelock, Vicki, Durr, Alexandra, Anderson, Karen E, Long, Jeffrey D, Wild, Edward J, Landwehrmeyer, G Bernhard, Leavitt, Blair R, Tabrizi, Sarah J, Doody, Rachelle

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Speech biomarkers in Huntington's disease: A cross‐sectional study in pre‐symptomatic, prodromal and early manifest stages von Kouba, Tomas, Frank, Wiebke, Tykalova, Tereza, Mühlbäck, Alzbeta, Klempíř, Jiří, Lindenberg, Katrin S., Landwehrmeyer, G. Bernhard, Rusz, Jan

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Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease von Lee, Jong-Min, Wheeler, Vanessa C., Chao, Michael J., Vonsattel, Jean Paul G., Pinto, Ricardo Mouro, Lucente, Diane, Abu-Elneel, Kawther, Ramos, Eliana Marisa, Mysore, Jayalakshmi Srinidhi, Gillis, Tammy, MacDonald, Marcy E., Gusella, James F., Harold, Denise, Stone, Timothy C., Escott-Price, Valentina, Han, Jun, Vedernikov, Alexey, Holmans, Peter, Jones, Lesley, Kwak, Seung, Mahmoudi, Mithra, Orth, Michael, Landwehrmeyer, G. Bernhard, Paulsen, Jane S., Dorsey, E. Ray, Shoulson, Ira, Myers, Richard H.

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Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset von McAllister, Branduff, Donaldson, Jasmine, Binda, Caroline S., Powell, Sophie, Chughtai, Uroosa, Edwards, Gareth, Stone, Joseph, Lobanov, Sergey, Elliston, Linda, Schuhmacher, Laura-Nadine, Rees, Elliott, Menzies, Georgina, Ciosi, Marc, Maxwell, Alastair, Chao, Michael J., Hong, Eun Pyo, Lucente, Diane, Wheeler, Vanessa, Lee, Jong-Min, MacDonald, Marcy E., Long, Jeffrey D., Aylward, Elizabeth H., Landwehrmeyer, G. Bernhard, Rosser, Anne E., Paulsen, Jane S., Williams, Nigel M., Gusella, James F., Monckton, Darren G., Allen, Nicholas D., Holmans, Peter, Jones, Lesley, Massey, Thomas H.

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Dorsolateral prefrontal cortex dysfunction in presymptomatic Huntington's disease: evidence from event-related fMRI von Wolf, Robert Christian, Vasic, Nenad, Schönfeldt-Lecuona, Carlos, Landwehrmeyer, G. Bernhard, Ecker, Daniel

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Suicidal ideation and suicidal behavior according to the C-SSRS in a European cohort of Huntington's disease gene expansion carriers von van Duijn, Erik, Vrijmoeth, Eslie M., Giltay, Erik J., Bernhard Landwehrmeyer, G.

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Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease von McAllister, Branduff, Gusella, James F., Landwehrmeyer, G. Bernhard, Lee, Jong-Min, MacDonald, Marcy E., Orth, Michael, Rosser, Anne E., Williams, Nigel M., Holmans, Peter, Jones, Lesley, Massey, Thomas H.

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Neuropsychiatric symptoms in a European Huntington's disease cohort (REGISTRY) von van Duijn, Erik, Craufurd, David, Hubers, Anna A M, Giltay, Erik J, Bonelli, Raphael, Rickards, Hugh, Anderson, Karen E, van Walsem, Marleen R, van der Mast, Rose C, Orth, Michael, Landwehrmeyer, G Bernhard

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Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues von Hoschek, Franziska, Natan, Julia, Wagner, Maximilian, Sathasivam, Kirupa, Abdelmoez, Alshaimaa, von Einem, Björn, Bates, Gillian P, Landwehrmeyer, G Bernhard, Neueder, Andreas

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Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy von Brown, Richard G., Lacomblez, Lucette, Landwehrmeyer, Bernard G., Bak, Thomas, Uttner, Ingo, Dubois, Bruno, Agid, Yves, Ludolph, Albert, Bensimon, Gilbert, Payan, Christine, Leigh, Nigel P.

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A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort von Weydt, Patrick, Soyal, Selma M, Landwehrmeyer, G Bernhard, Patsch, Wolfgang

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Ubiquitination and the proteasome rather than caspase‐3‐mediated C‐terminal cleavage are involved in the EAAT2 degradation by staurosporine‐induced cellular stress von Voss, Timo‐Daniel, Gerget, Maria, Linkus, Birgit, Einem, Bjoern, Landwehrmeyer, G. Bernhard, Lewerenz, Jan

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Olfactory screening of Parkinson's Disease patients and healthy subjects in China and Germany: A study of cross-cultural adaptation of the Sniffin' Sticks 12-identification test von Pinkhardt, Elmar H, Liu, Huijing, Ma, Di, Chen, Jing, Pachollek, Adrian, Kunz, Martin S, Kassubek, Jan, Ludolph, Albert C, Huang, Yining, Chen, Haibo, Landwehrmeyer, G Bernhard, Wang, Zhaoxia, Su, Wen

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