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26 results on '"Tchikviladzé, Maya"'

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1. Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions

2. Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

3. Successful thrombectomy is beneficial in patients with pre-stroke disability: Results from an international multicenter cohort study

4. Thrombectomy for Basilar Artery Occlusion with Mild Symptoms

6. Higher Annual Operator Volume Is Associated With Better Reperfusion Rates in Stroke Patients Treated by Mechanical Thrombectomy: The ETIS Registry

7. Motor neuron involvement threatens survival in spinocerebellar ataxia type 1

9. Successful Reperfusion With Mechanical Thrombectomy Is Associated With Reduced Disability and Mortality in Patients With Pretreatment Diffusion-Weighted Imaging–Alberta Stroke Program Early Computed Tomography Score ≤6

10. Low cancer prevalence in polyglutamine expansion diseases

11. Clinical and genetic characteristics of late-onset Huntington's disease

12. A diagnostic flow chart for POLG-related diseases based on signs sensitivity and specificity

15. Quantitative Assessment of the Evolution of Cerebellar Signs in Spinocerebellar Ataxias

16. Predictors of Parenchymal Hematoma After Mechanical Thrombectomy

17. Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study

18. Cognitive decline in Huntington's disease expansion gene carriers

19. Mechanical Thrombectomy for Minor and Mild Stroke Patients Harboring Large Vessel Occlusion in the Anterior Circulation

20. Mortality and Disability According to Baseline Blood Pressure in Acute Ischemic Stroke Patients Treated by Thrombectomy: A Collaborative Pooled Analysis

22. Quantifiable evaluation of cerebellar signs in children

23. A diagnostic flow chart forPOLG-related diseases based on signs sensitivity and specificity

24. A Diagnostic Flowchart For POLG Related Diseases Based On Signs Sensitivity And Specificity (P3.299)

25. Intermediate repeat expansions of TBPand STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

26. Factors Influencing Disease Progression in Autosomal Dominant Cerebellar Ataxia and Spastic Paraplegia.

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