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2. The Huntington's Disease Gene Discovery

4. Progressive alterations in white matter microstructure across the timecourse of Huntington's disease

7. CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy‐like Phenotype

8. An MDS Evidence‐Based Review on Treatments for Huntington's Disease

9. Relating quantitative 7T MRI across cortical depths to cytoarchitectonics, gene expression and connectomics

13. Longitudinal Structural MRI in Neurologically Healthy Adults

14. Expression of mutant exon 1 huntingtin fragments in human neural stem cells and neurons causes inclusion formation and mitochondrial dysfunction

15. Predicting clinical diagnosis in Huntington's disease: An imaging polymarker

16. Characterizing White Matter in Huntington's Disease

18. Movement Disorder Society Task Force Viewpoint: Huntington's Disease Diagnostic Categories

21. An image-based model of brain volume biomarker changes in Huntington's disease

25. DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases

26. Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

31. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

32. A longitudinal study of magnetic resonance spectroscopy Huntington's disease biomarkers

38. The structural correlates of functional deficits in early huntington's disease

39. Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry

40. The structural involvement of the cingulate cortex in premanifest and early Huntington's disease

41. Early changes in white matter pathways of the sensorimotor cortex in premanifest Huntington's disease

48. P3‐377: A novel pathogenic pathway of immune activation detectable before cinical onset in Huntington's disease

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