Misfolded PrP and a novel mechanism of proteasome inhibition

Por Andre, Ralph, Tabrizi, Sarah J
Publicado em 2012

Gene suppression approaches to neurodegeneration

Por Ghosh, Rhia, Tabrizi, Sarah J.
Publicado no Alzheimers Res Ther (2017)

Targets for future clinical trials in Huntington's disease: What's in the pipeline?

Por Wild, Edward J, Tabrizi, Sarah J
Publicado no Mov Disord (2014)

The application of NMR-based metabonomics in neurological disorders

Por Holmes, Elaine, Tsang, Tsz M., Tabrizi, Sarah J.
Publicado em 2012

Prion degradation pathways: Potential for therapeutic intervention

Por Goold, Rob, McKinnon, Chris, Tabrizi, Sarah J.
Publicado no Mol Cell Neurosci (2015)

George Huntington: a legacy of inquiry, empathy and hope

Por Wexler, Alice, Wild, Edward J., Tabrizi, Sarah J.
Publicado no Brain (2016)

Test–Retest Reliability of Measures Commonly Used to Measure Striatal Dysfunction across Multiple Testing Sessions: A Longitudinal Study

Por Palmer, Clare E., Langbehn, Douglas, Tabrizi, Sarah J., Papoutsi, Marina
Publicado no Front Psychol (2018)

Measuring Compensation in Neurodegeneration using MRI

Por Gregory, Sarah, Long, Jeffrey. D, Tabrizi, Sarah J., Rees, Geraint
Publicado no Curr Opin Neurol (2017)

Mutant Huntingtin Does Not Affect the Intrinsic Phenotype of Human Huntington’s Disease T Lymphocytes

Por Miller, James R. C., Träger, Ulrike, Andre, Ralph, Tabrizi, Sarah J.
Publicado no PLoS One (2015)

Diffusion imaging in Huntington’s disease: comprehensive review

Por Estevez-Fraga, Carlos, Scahill, Rachael, Rees, Geraint, Tabrizi, Sarah J, Gregory, Sarah
Publicado no J Neurol Neurosurg Psychiatry (2021)

Stimulating neural plasticity with real‐time fMRI neurofeedback in Huntington's disease: A proof of concept study

Por Papoutsi, Marina, Weiskopf, Nikolaus, Langbehn, Douglas, Reilmann, Ralf, Rees, Geraint, Tabrizi, Sarah J
Publicado no Hum Brain Mapp (2017)

Juvenile Huntington's disease: a population-based study using the General Practice Research Database

Por Douglas, Ian, Evans, Stephen, Rawlins, Michael D, Smeeth, Liam, Tabrizi, Sarah J, Wexler, Nancy S
Publicado em 2013

Alternative fates of newly formed PrP(Sc) upon prion conversion on the plasma membrane

Por Goold, Rob, McKinnon, Chris, Rabbanian, Samira, Collinge, John, Schiavo, Giampietro, Tabrizi, Sarah J.
Publicado em 2013

Working Memory-Related Effective Connectivity in Huntington’s Disease Patients

Por Lahr, Jacob, Minkova, Lora, Tabrizi, Sarah J., Stout, Julie C., Klöppel, Stefan, Scheller, Elisa
Publicado no Front Neurol (2018)

Functional compensation of motor function in pre-symptomatic Huntington's disease

Por Klöppel, Stefan, Draganski, Bogdan, Siebner, Hartwig R., Tabrizi, Sarah J., Weiller, Cornelius, Frackowiak, Richard S. J.
Publicado em 2009

Abnormal peripheral chemokine profile in Huntington’s disease

Por Wild, Edward, Magnusson, Anna, Lahiri, Nayana, Krus, Ulrika, Orth, Michael, Tabrizi, Sarah J, Björkqvist, Maria
Publicado em 2011

Prevalence of adult Huntington's disease in the UK based on diagnoses recorded in general practice records

Por Evans, Stephen JW, Douglas, Ian, Rawlins, Michael D, Wexler, Nancy S, Tabrizi, Sarah J, Smeeth, Liam
Publicado em 2013

Interregional compensatory mechanisms of motor functioning in progressing preclinical neurodegeneration

Por Scheller, Elisa, Abdulkadir, Ahmed, Peter, Jessica, Tabrizi, Sarah J., Frackowiak, Richard S.J., Klöppel, Stefan
Publicado em 2013

Overlap between age-at-onset and disease-progression determinants in Huntington disease

Por Aziz, N. Ahmad, van der Burg, Jorien M.M., Tabrizi, Sarah J., Landwehrmeyer, G. Bernhard
Publicado no Neurology (2018)

Wild-type huntingtin regulates human macrophage function

Por O’Regan, Grace C., Farag, Sahar H., Ostroff, Gary R., Tabrizi, Sarah J., Andre, Ralph
Publicado no Sci Rep (2020)