68 results on '"Tabrizi, Sarah J."'
Search Results
2. The Huntington's Disease Gene Discovery
3. Huntington disease alters the actionable information in plasma extracellular vesicles
4. Progressive alterations in white matter microstructure across the timecourse of Huntington's disease
5. Disentangling the Connection Between Neurodevelopment and Neurodegeneration in Huntington's Disease
6. “On Chorea”: 150 Years of the Beginning of Hope
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
10. Tracking Huntingtonʼs Disease Progression Using Motor, Functional, Cognitive, and Imaging Markers
11. Disease Onset in Huntington's Disease: When Is the Conversion?
12. Composite UHDRS Correlates With Progression of Imaging Biomarkers in Huntington's Disease
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
17. One decade ago, one decade ahead in huntington's disease
18. Movement Disorder Society Task Force Viewpoint: Huntington's Disease Diagnostic Categories
19. Response to the letter to the editor by Reilmann et al referring to our article titled “Motor cortex synchronization influences the rhythm of motor performance in premanifest Huntington's disease”
20. Natural biological variation of white matter microstructure is accentuated in Huntington's disease
21. An image-based model of brain volume biomarker changes in Huntington's disease
22. Predicting clinical diagnosis in Huntington's disease: An imaging polymarker
23. Motor cortex synchronization influences the rhythm of motor performance in premanifest huntington's disease
24. Stimulating neural plasticity with real-time fMRI neurofeedback in Huntington's disease: A proof of concept study
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
27. Huntington's Disease and Other Choreas
28. Validation of a prognostic index for Huntington's disease
29. Cerebrospinal fluid total tau concentration predicts clinical phenotype in Huntington's disease
30. Laquinimod dampens hyperactive cytokine production in Huntington's disease patient myeloid cells
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
33. Basal ganglia-cortical structural connectivity in Huntington's disease
34. Targets for future clinical trials in Huntington's disease: What's in the pipeline?
35. Cerebellar abnormalities in Huntington's disease: A role in motor and psychiatric impairment?
36. The cognitive burden in Huntington's disease: Pathology, phenotype, and mechanisms of compensation
37. Selective executive dysfunction but intact risky decision-making in early Huntington's disease
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
42. An ITPR1 gene deletion causes spinocerebellar ataxia 15/16: A genetic, clinical and radiological description
43. Abnormal explicit but normal implicit sequence learning in premanifest and early Huntington's disease
44. Microglial activation in regions related to cognitive function predicts disease onset in Huntington's disease: A multimodal imaging study
45. Rate and acceleration of whole-brain atrophy in premanifest and early Huntington's disease
46. Saccadometry of Conditional Rules in Presymptomatic Huntington's Disease
47. Whole‐brain atrophy as a measure of progression in premanifest and early Huntington's disease
48. P3‐377: A novel pathogenic pathway of immune activation detectable before cinical onset in Huntington's disease
49. Huntington's disease phenocopies are clinically and genetically heterogeneous
50. Spinocerebellar ataxia type 17: Extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging
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