First German Academy for Further Medical Training on Rare Diseases (<it>FAKSE</it>, <url>http://www.fakse.info</url>)

di Giehl Julia, Graessner Holm, Riess Olaf
Pubblicazione 2012-11-01

First German Academy for Further Medical Training on Rare Diseases (FAKSE, http://www.fakse.info)

di Giehl, Julia, Graessner, Holm, Riess, Olaf
Pubblicazione 2012

The Guanine Nucleotide Exchange Factor Kalirin-7 Is a Novel Synphilin-1 Interacting Protein and Modifies Synphilin-1 Aggregate Transport and Formation

di Tsai, Yu-Chun, Riess, Olaf, Soehn, Anne S., Nguyen, Huu Phuc
Pubblicazione 2012

SNCA overexpression disturbs hippocampal gene expression trajectories in midlife

di Hentrich, Thomas, Wassouf, Zinah, Riess, Olaf, Schulze-Hentrich, Julia M.
Pubblicato in Aging (Albany NY) (2018)

Two cases of variant late infantile ceroid lipofuscinosis in Jordan

di Nafi, Omar, Ramadan, Bashar, Riess, Olaf, Buchert, Rebecca, Froukh, Tawfiq
Pubblicato in World J Clin Cases (2019)

Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients

di Tsai, Yu-Chun, Metzger, Silke, Riess, Olaf, Soehn, Anne S, Nguyen, Huu Phuc
Pubblicazione 2012

Reduced Motivation in the BACHD Rat Model of Huntington Disease Is Dependent on the Choice of Food Deprivation Strategy

di Jansson, Erik Karl Håkan, Clemens, Laura Emily, Riess, Olaf, Nguyen, Huu Phuc
Pubblicazione 2014

The BACHD Rat Model of Huntington Disease Shows Signs of Fronto-Striatal Dysfunction in Two Operant Conditioning Tests of Short-Term Memory

di Clemensson, Erik Karl Håkan, Clemensson, Laura Emily, Riess, Olaf, Nguyen, Huu Phuc
Pubblicato in PLoS One (2017)

Autophagy induction reduces mutant ataxin-3 levels and toxicity in a mouse model of spinocerebellar ataxia type 3

di Menzies, Fiona M., Huebener, Jeannette, Renna, Maurizio, Bonin, Michael, Riess, Olaf, Rubinsztein, David C.
Pubblicazione 2010

Cerebellar Soluble Mutant Ataxin-3 Level Decreases during Disease Progression in Spinocerebellar Ataxia Type 3 Mice

di Nguyen, Huu Phuc, Hübener, Jeannette, Weber, Jonasz Jeremiasz, Grueninger, Stephan, Riess, Olaf, Weiss, Andreas
Pubblicazione 2013

Complexin-1 and Foxp1 Expression Changes Are Novel Brain Effects of Alpha-Synuclein Pathology

di Gispert, Suzana, Kurz, Alexander, Brehm, Nadine, Rau, Katrin, Walter, Michael, Riess, Olaf, Auburger, Georg
Pubblicato in Mol Neurobiol (2014)

Further investigation of phenotypes and confounding factors of progressive ratio performance and feeding behavior in the BACHD rat model of Huntington disease

di Clemensson, Erik Karl Håkan, Clemensson, Laura Emily, Fabry, Benedikt, Riess, Olaf, Nguyen, Huu Phuc
Pubblicato in PLoS One (2017)

Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease

di Che, Hong Van B, Metzger, Silke, Portal, Esteban, Deyle, Carolin, Riess, Olaf, Nguyen, Huu Phuc
Pubblicazione 2011

Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synuclein

di Kuhn, Melanie, Haebig, Karina, Bonin, Michael, Ninkina, Natalia, Buchmann, Vladimir L., Poths, Sven, Riess, Olaf
Pubblicazione 2007

The calpain-suppressing effects of olesoxime in Huntington's disease

di Weber, Jonasz J., Ortiz Rios, Midea M., Riess, Olaf, Clemens, Laura E., Nguyen, Huu P.
Pubblicato in Rare Dis (2016)

Distinct Stress Response and Altered Striatal Transcriptome in Alpha-Synuclein Overexpressing Mice

di Wassouf, Zinah, Hentrich, Thomas, Casadei, Nicolas, Jaumann, Mirko, Knipper, Marlies, Riess, Olaf, Schulze-Hentrich, Julia M.
Pubblicato in Front Neurosci (2019)

Divalproex sodium modulates nuclear localization of ataxin‐3 and prevents cellular toxicity caused by expanded ataxin‐3

di Wang, Zi‐Jian, Hanet, Aoife, Weishäupl, Daniel, Martins, Inês M., Sowa, Anna S., Riess, Olaf, Schmidt, Thorsten
Pubblicato in CNS Neurosci Ther (2018)

The Alteration of Emotion Regulation Precedes the Deficits in Interval Timing in the BACHD Rat Model for Huntington Disease

di Garces, Daniel, El Massioui, Nicole, Lamirault, Charlotte, Riess, Olaf, Nguyen, Huu P., Brown, Bruce L., Doyère, Valérie
Pubblicato in Front Integr Neurosci (2018)

High-Throughput Homogeneous Mass Cleave Assay Technology for the Diagnosis of Autosomal Recessive Parkinson's Disease

di Schroeder, Christopher, Walter, Michael, Berg, Daniela, Leitner, Petra, Bauer, Peter, Kohl, Zacharias, Winkler, Jürgen, Riess, Olaf, Bonin, Michael
Pubblicazione 2008

The V471A Polymorphism in Autophagy-Related Gene ATG7 Modifies Age at Onset Specifically in Italian Huntington Disease Patients

di Metzger, Silke, Walter, Carolin, Riess, Olaf, Roos, Raymund A. C., Nielsen, Jørgen E., Craufurd, David, Nguyen, Huu Phuc
Pubblicazione 2013