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39 results on '"Jeroen J de Vries"'

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1. Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease

2. A resting-state fMRI pattern of spinocerebellar ataxia type 3 and comparison with 18F-FDG PET

3. The cerebral metabolic topography of spinocerebellar ataxia type 3

4. Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxia

5. A resting-state fMRI pattern of spinocerebellar ataxia type 3 and comparison with F-18-FDG PET

6. Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3

7. Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease Severity

8. CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3

9. Inborn Errors of Metabolism in Adults: Two Patients with Movement Disorders Caused by Glutaric Aciduria Type 1

10. How to detect late-onset inborn errors of metabolism in patients with movement disorders - A modern diagnostic approach

11. Not every excessive startle is hyperekplexia, the curious case of SOD1

12. A detailed description of the phenotypic spectrum of North Sea Progressive Myoclonus Epilepsy in a large cohort of seventeen patients

13. The cerebral metabolic topography of spinocerebellar ataxia type 3

14. Neurofilaments as blood biomarkers at the preataxic and ataxic stage of spinocerebellar ataxia type 3: a cross-species analysis in humans and mice

15. On the distribution of intranuclear and cytoplasmic aggregates in the brainstem of patients with spinocerebellar ataxia type 2 and 3

16. Reliability of phenotypic early-onset ataxia assessment: a pilot study

17. Ramsay hunt syndrome: Clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation

18. On the distribution of intranuclear and cytoplasmic aggregates in the brainstem of patients with spinocerebellar ataxia type 2 and 3

19. Typical cerebral metabolic patterns in neurodegenerative brain diseases

20. The Alzheimer's disease-related glucose metabolic brain pattern

21. Ramsay Hunt syndrome: clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation

22. Blood-brain barrier P-glycoprotein function decreases in specific brain regions with aging: a possible role in progressive neurodegeneration

23. Visual processing impairments and decrements in regional brain activity in Alzheimer's disease

24. Visual perceptual functions predict instrumental activities of daily living in patients with dementia

25. Successful surgical treatment of an arachnoid cyst inducing a Holmes' tremor

26. Symptoms mimicking dementia in a 60-year-old woman with bipolar disorder: a case report

27. Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3.

28. Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and Duration.

30. Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3.

32. Cerebellar volumetry in ataxias: Relation to ataxia severity and duration.

33. Stage-dependent biomarker changes in spinocerebellar ataxia type 3.

34. The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors.

35. Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease Severity.

36. Polyglutamine-Expanded Ataxin-3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood.

37. Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice.

38. Impact of tumour invasion on seminal vesicles mobility in radiotherapy of prostate cancer.

39. Solution titration by wall deprotonation during capillary filling of silicon oxide nanochannels.

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