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3. Association of peripheral neuropathy with sleep-related breathing disorders in myotonic dystrophies

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

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

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

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

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

9. Fractionation ameliorates changes in hippocampal neurogenesis after irradiation

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

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

12. Expression of neuronal migratory phenotype marker – doublecortin correlates with motility characteristics of normal and transformed astrocytic cell lines and human glial tumors

14. Anther Culture of Basmati 370 At IRRI. A. Gamma Ray-Induced Green Plant Regeneration

15. Anther Culture of Basmati 370 At IRRI. B. Effect of Glucose in Anther Culture of Irradiated Basmati 370

16. Seeds of Anther Culture-Derived Lines Are Available At IRRI

17. Clinical validity of MR based program for analysis of fluid/brain index of posterior cranial fossa structures in patients with spinocerebellar ataxia

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

23. The Third International Stroke Trial: Thrombolysis (IST-3) in Poland: Are we recruiting the right patients?

28. Effect of cyclic adenosine monophosphate on the G protein-dependent inward rectifier K+-like channel current in medial prefrontal cortex pyramidal neurons

29. Responsiveness of different rating instruments in spinocerebellar ataxia patients

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

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

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

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

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

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

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