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8. Association of CAG Repeats With Long-term Progression in Huntington Disease

9. Identification of symbol digit modality test score extremes in Huntington's disease

10. Apathy associated with impaired recognition of happy facial expressions in Huntington's disease

11. MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1

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

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

20. Quantitative motor phenotype assessment in pre-manifest and symptomatic Huntington's disease: tongue force analysis differentiates between disease stages and provides high phenotype correlation. Cross sectional results from the TRACK-HD Study

22. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

24. Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy

25. β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease

26. Attention-deficit/hyperactivity disorder in childhood epilepsy: a neuropsychological and functional imaging study

27. Discrepancies in reporting the CAG repeat lengths for Huntington's disease

33. Q-motor – Quantitative motor assessments: Potential novel endpoints for clinical trials in pre-manifest and symptomatic Huntington's disease – 36 months longitudinal results from the multicenter TRACK-HD study

38. F14 Speeded tapping assesses progression of huntington's disease within one year—results from the track-HD study

40. H06 Cross sectional and longitudinal 3T magnetic resonance spectroscopy in a TRACK-HD cohort of individuals with premanifest and early Huntington's disease

42. Finger tapping as an objective motor phenotype marker in pre-manifest and symptomatic Huntington's disease – cross-sectional results from the TRACK-HD Study

43. Quantitative motor phenotype assessment in pre-manifest and symptomatic Huntington's disease: tongue force analysis differentiates between disease stages and provides high phenotype correlation. Cross sectional results from the TRACK-HD Study

44. Sensitivity of gait analysis to detect motor phenotype in pre-manifest and manifest Huntington's disease – cross-sectional results from the TRACK-HD Study

46. On Chorea – quantitative and objective analysis – cross-sectional results of the TRACK-HD Study

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