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17 results on '"Rakowicz, M"'

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

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

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

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

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

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

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

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

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

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

11. Responsiveness of different rating instruments in spinocerebellar ataxia patients

12. SCA Functional Index: A useful compound performance measure for spinocerebellar ataxia

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

14. Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrument

15. Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data

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

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

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