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1. Design optimization for clinical trials in early-stage manifest Huntington's disease.

2. Visuospatial Processing Deficits Linked to Posterior Brain Regions in Premanifest and Early Stage Huntington's Disease.

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3. A Metabolic Study of Huntington's Disease.

4. Short-interval observational data to inform clinical trial design in Huntington's disease.

5. A 24-Hour Study of the Hypothalamo-Pituitary Axes in Huntington's Disease.

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

7. Longitudinal Diffusion Tensor Imaging Shows Progressive Changes in White Matter in Huntington's Disease.

8. Inconsistent emotion recognition deficits across stimulus modalities in Huntington׳s disease.

9. Plasma melatonin is reduced in Huntington's disease.

10. The potential of composite cognitive scores for tracking progression in Huntington's disease.

11. Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data.

12. Emotional face recognition deficits and medication effects in pre-manifest through stage-II Huntington's disease.

13. Corpus callosal atrophy in premanifest and early Huntington's disease.

14. Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression.

15. Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease.

16. Emotion recognition in Huntington's disease: a systematic review.

17. Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data.

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

19. Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis.

20. Rate and acceleration of whole-brain atrophy in premanifest and early Huntington's disease.

21. Automated quantification of caudate atrophy by local registration of serial MRI: evaluation and application in Huntington's disease.

22. Whole-brain atrophy as a measure of progression in premanifest and early Huntington's disease.

23. Defective emotion recognition in early HD is neuropsychologically and anatomically generic.

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

25. TRACK and attack Huntington's disease