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3. Impairments of social cognition significantly predict the progression of functional decline in Huntington's disease: A 6-year follow-up study.

10. Clinical and genetic characteristics of late-onset Huntington's disease

13. Endophenotypical drift in Huntington’s disease:a 5-year follow-up study

14. Hybrid 2-[18F] FDG PET/MRI in premanifest Huntington's disease gene-expansion carriers:The significance of partial volume correction

15. Cognitive Screening Tests in Huntington Gene Mutation Carriers:Examining the Validity of the Mini-Mental State Examination and the Montreal Cognitive Assessment

16. Early Intrathecal T Helper 17.1 Cell Activity in Huntington Disease

17. Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study

18. Hybrid 2-[18F] FDG PET/MRI in premanifest Huntington's disease gene-expansion carriers: The significance of partial volume correction.

20. Cognitive Screening Tests in Huntington Gene Mutation Carriers: Examining the Validity of the Mini-Mental State Examination and the Montreal Cognitive Assessment.

22. Defining active progressive multiple sclerosis

23. SCA28:Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy

24. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

25. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

26. Defining active progressive multiple sclerosis

29. Social Cognition, Executive Functions and Self-Report of Psychological Distress in Huntington's Disease

30. Selected CSF biomarkers indicate no evidence of early neuroinflammation in Huntington disease

31. Personality Traits in Huntington's Disease:An Exploratory Study of Gene Expansion Carriers and Non-Carriers

32. Liver function in Huntington's disease assessed by blood biochemical analyses in a clinical setting

33. Do I misconstrue?:Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease

36. SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy

39. Assessing Impairment of Executive Function and Psychomotor Speed in Premanifest and Manifest Huntington's Disease Gene-expansion Carriers

41. A clinical classification acknowledging neuropsychiatric and cognitive impairment in Huntingtons disease

42. Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease

46. Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2

50. Identification of genetic variants associated with Huntington's disease progression

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