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

Por Weydt, Patrick, Soyal, Selma M, Landwehrmeyer, G Bernhard, Patsch, Wolfgang
Publicado em 2014

Fast-to-Slow Transition of Skeletal Muscle Contractile Function and Corresponding Changes in Myosin Heavy and Light Chain Formation in the R6/2 Mouse Model of Huntington’s Disease...

Por Hering, Tanja, Braubach, Peter, Landwehrmeyer, G. Bernhard, Lindenberg, Katrin S., Melzer, Werner
Publicado no PLoS One (2016)

Utilisation of Healthcare and Associated Services in Huntington’s disease: a data mining study

Por Busse, Monica, Al-Madfai, Dr. Hasan, Kenkre, Joyce, Landwehrmeyer, G. Bernhard, Bentivoglio, AnnaRita, Rosser, Anne
Publicado em 2011

Stability effects on results of diffusion tensor imaging analysis by reduction of the number of gradient directions due to motion artifacts: an application to presymptomatic Huntin...

Por Müller, Hans-Peter, Süssmuth, Sigurd D., Landwehrmeyer, G. Bernhard, Ludolph, Albert, Tabrizi, Sarah J, Kloppel, Stefan, Kassubek, Jan
Publicado em 2012

The gene coding for PGC-1α modifies age at onset in Huntington's Disease

Por Weydt, Patrick, Soyal, Selma M, Gellera, Cinzia, DiDonato, Stefano, Weidinger, Claus, Oberkofler, Hannes, Landwehrmeyer, G Bernhard, Patsch, Wolfgang
Publicado em 2009

Current Pharmacological Management in Juvenile Huntington’s Disease

Por Robertson, Lisa, Santini, Helen, O'Donovan, Kirsty L, Squitieri, Ferdinando, Barker, Roger A, Rakowicz, Maria, Landwehrmeyer, G. Bernhard, Quarrell, Oliver
Publicado em 2012

Two-Point Magnitude MRI for Rapid Mapping of Brown Adipose Tissue and Its Application to the R6/2 Mouse Model of Huntington Disease

Por Lindenberg, Katrin S., Weydt, Patrick, Müller, Hans-Peter, Bornstedt, Axel, Ludolph, Albert C., Landwehrmeyer, G. Bernhard, Rottbauer, Wolfgang, Kassubek, Jan, Rasche, Volker
Publicado em 2014

Magnetic resonance perfusion imaging of resting-state cerebral blood flow in preclinical Huntington's disease

Por Wolf, Robert C, Grön, Georg, Sambataro, Fabio, Vasic, Nenad, Wolf, Nadine D, Thomann, Philipp A, Saft, Carsten, Landwehrmeyer, G Bernhard, Orth, Michael
Publicado em 2011

Discrepancies in reporting the CAG repeat lengths for Huntington's disease

Por Quarrell, Oliver W, Handley, Olivia, O'Donovan, Kirsty, Dumoulin, Christine, Ramos-Arroyo, Maria, Biunno, Ida, Bauer, Peter, Kline, Margaret, Landwehrmeyer, G Bernhard
Publicado em 2012

Observing Huntington’s Disease: the European Huntington’s Disease Network’s REGISTRY

Por Orth, Michael, Handley, Olivia J, Schwenke, Carsten, Dunnett, Stephen B., Craufurd, David, Ho, Aileen K, Wild, Edward, Tabrizi, Sarah J, Landwehrmeyer, G. Bernhard
Publicado em 2011

High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington’s disease expansion mutation carriers shows normal mitochondrial respiratory function

Por Buck, Eva, Zügel, Martina, Schumann, Uwe, Merz, Tamara, Gumpp, Anja M., Witting, Anke, Steinacker, Jürgen M., Landwehrmeyer, G. Bernhard, Weydt, Patrick, Calzia, Enrico, Lindenberg, Katrin S.
Publicado no PLoS One (2017)

NMDA receptor gene variations as modifiers in Huntington disease: a replication study

Por Saft, Carsten, Epplen, Jörg T., Wieczorek, Stefan, Landwehrmeyer, G. Bernhard, Roos, Raymund A.C., de Yebenes, Justo Garcia, Dose, Matthias, Tabrizi, Sarah J, Craufurd, David, Arning, Larissa
Publicado em 2011

Intact sensory-motor network structure and function in far from onset premanifest Huntington’s disease

Por Gorges, Martin, Müller, Hans-Peter, Mayer, Isabella Maria Sophie, Grupe, Gesa Sophie, Kammer, Thomas, Grön, Georg, Kassubek, Jan, Landwehrmeyer, G. Bernhard, Wolf, Robert Christian, Orth, Michael
Publicado no Sci Rep (2017)

Evaluating multicenter DTI data in Huntington's disease on site specific effects: An ex post facto approach()

Por Müller, Hans-Peter, Grön, Georg, Sprengelmeyer, Reiner, Kassubek, Jan, Ludolph, Albert C., Hobbs, Nicola, Cole, James, Roos, Raymund A.C., Duerr, Alexandra, Tabrizi, Sarah J., Landwehrmeyer, G. Bernhard, Süssmuth, Sigurd D.
Publicado em 2013

Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease

Por Müller, Hans-Peter, Kassubek, Jan, Grön, Georg, Sprengelmeyer, Reiner, Ludolph, Albert C, Klöppel, Stefan, Hobbs, Nicola Z, Roos, Raymund AC, Duerr, Alexandra, Tabrizi, Sarah J, Orth, Michael, Süssmuth, Sigurd D, Landwehrmeyer, G Bernhard
Publicado em 2014

Medication Use in Early-HD Participants in Track-HD: an Investigation of its Effects on Clinical Performance

Por Keogh, Ruth, Frost, Chris, Owen, Gail, Daniel, Rhian M., Langbehn, Doug R., Leavitt, Blair, Durr, Alexandra, Roos, Raymund A.C., Landwehrmeyer, G. Bernhard, Reilmann, Ralf, Borowsky, Beth, Stout, Julie, Craufurd, David, Tabrizi, Sarah J.
Publicado no PLoS Curr (2016)

Assessment of Motor Symptoms and Functional Impact in Prodromal and Early Huntington Disease

Por Vaccarino, Anthony L, Sills, Terrence, Anderson, Karen E., Biglan, Kevin, Borowsky, Beth, Giuliano, Joseph, Guttman, Mark, Ho, Aileen K, Kennard, Christopher, Kupchak, Peter, Landwehrmeyer, G. Bernhard, Michell, Andrew, Paulsen, Jane S., Reilmann, Ralf, van Kammen, Daniel P, Warner, John H., Evans, Ken
Publicado em 2011

Compensation in Preclinical Huntington's Disease: Evidence From the Track-On HD Study

Por Klöppel, Stefan, Gregory, Sarah, Scheller, Elisa, Minkova, Lora, Razi, Adeel, Durr, Alexandra, Roos, Raymund A.C., Leavitt, Blair R., Papoutsi, Marina, Landwehrmeyer, G. Bernhard, Reilmann, Ralf, Borowsky, Beth, Johnson, Hans, Mills, James A., Owen, Gail, Stout, Julie, Scahill, Rachael I., Long, Jeffrey D., Rees, Geraint, Tabrizi, Sarah J.
Publicado no EBioMedicine (2015)

An exploratory double-blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington’s disease

Por Süssmuth, Sigurd D, Haider, Salman, Landwehrmeyer, G Bernhard, Farmer, Ruth, Frost, Chris, Tripepi, Giovanna, Andersen, Claus A, Di Bacco, Marco, Lamanna, Claudia, Diodato, Enrica, Massai, Luisa, Diamanti, Daniela, Mori, Elisa, Magnoni, Letizia, Dreyhaupt, Jens, Schiefele, Karin, Craufurd, David, Saft, Carsten, Rudzinska, Monika, Ryglewicz, Danuta, Orth, Michael, Brzozy, Sebastian, Baran, Anna, Pollio, Giuseppe, Andre, Ralph, Tabrizi, Sarah J, Darpo, Borje, Westerberg, Goran
Publicado no Br J Clin Pharmacol (2015)

TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease

Por Lee, Ji-Hyun, Lee, Jong-Min, Ramos, Eliana Marisa, Gillis, Tammy, Mysore, Jayalakshmi S., Kishikawa, Shotaro, Hadzi, Tiffany, Hendricks, Audrey E., Hayden, Michael R., Morrison, Patrick J., Nance, Martha, Ross, Christopher A., Margolis, Russell L., Squitieri, Ferdinando, Gellera, Cinzia, Gomez-Tortosa, Estrella, Ayuso, Carmen, Suchowersky, Oksana, Trent, Ronald J., McCusker, Elizabeth, Novelletto, Andrea, Frontali, Marina, Jones, Randi, Ashizawa, Tetsuo, Frank, Samuel, Saint-Hilaire, Marie-Helene, Hersch, Steven M., Rosas, Herminia D., Lucente, Diane, Harrison, Madaline B., Zanko, Andrea, Abramson, Ruth K., Marder, Karen, Sequeiros, Jorge, Landwehrmeyer, G. Bernhard, Network, Ira Shoulson, Myers, Richard H., MacDonald, Marcy E., Gusella, James F.
Publicado em 2012