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

3. Prediction of Survival With Long-Term Disease Progression in Most Common Spinocerebellar Ataxia

4. Clinical evaluation of the effectiveness of teleneuroforma – A home rehabilitation tool for patients with Huntington's disease

5. Suicidal ideation in a European Huntington's disease population

7. The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients

10. Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6

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

12. NMDA receptor gene variations as modifiers in Huntington disease: a replication study

13. Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

14. Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

15. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

16. A Randomized, Double-blind, Placebo-Controlled Study of Latrepirdine in Patients With Mild to Moderate Huntington Disease

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

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

19. The natural history of spinocerebellar ataxia type 1, 2, 3 and 6 : A 2-year follow-up study

20. NMDA receptor gene variations as modifiers in Huntington disease

22. Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

23. Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6

28. Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6

29. Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings.

30. Depression comorbidity in spinocerebellar ataxia

31. Depression comorbidity in spinocerebellar ataxia.

32. Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings.

33. The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.

34. Self-rated health status in spinocerebellar ataxia--results from a European multicenter study.

35. Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

36. Responsiveness of different rating instruments in spinocerebellar ataxia patients.

37. Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

38. Responsiveness of different rating instruments in spinocerebellar ataxia patients.

39. Self-rated health status in spinocerebellar ataxia--results from a European multicenter study.

40. SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia.

41. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.

42. Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.

43. Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.

44. SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia.

45. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.

46. Scale for the assessment and rating of ataxia: development of a new clinical scale.

47. Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients.

48. Scale for the assessment and rating of ataxia: development of a new clinical scale.

49. Inventory of Non-Ataxia Signs (INAS): Validation of a New Clinical Assessment Instrument

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