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1. Expertise in surgical neuro-oncology. Results of a survey by the EANS neuro-oncology section

2. An Artificial Intelligence (AI) Framework to Predict Operational Excellence: UAE Case Study

3. Expertise in Surgical Neuro-oncology. Results of a Survey by the EANS Neuro-oncology Section.

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

15. Comparative assessment of attitudes among medical and dental professionals in Saudi Arabia toward e-professionalism using the SMEPROF-S scale.

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

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

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

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

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

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

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

31. Fractionation ameliorates changes in hippocampal neurogenesis after irradiation

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

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

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

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

41. Depression comorbidity in spinocerebellar ataxia

42. Depression comorbidity in spinocerebellar ataxia.

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

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

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

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

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

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

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

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