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

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

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

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

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

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

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

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

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

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

12. NMDA receptor gene variations as modifiers in Huntington disease

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

14. Depression comorbidity in spinocerebellar ataxia

15. Depression comorbidity in spinocerebellar ataxia.

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

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

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

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

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

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

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

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

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

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

29. Responsiveness of different rating instruments in spinocerebellar ataxia patients

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

34. SCA Functional Index

35. OCCURRENCE OF AUSTRALIA ANTIGEN IN PATIENTS WITH DOWN'S SYNDROME IN POLAND.

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

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

44. MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes,Zespół MELAS--mitochondrialna encefalomiopatia z kwasica mleczanowa i epizodami udaropodobnymi: przypadki potwierdzone biochemicznie i molekularnie oraz diagnostyka róznicowa przyczyn udarów

47. Responsiveness of different rating instruments in spinocerebellar ataxia patients

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

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

50. Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.

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