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319 results on '"Orsucci, Daniele"'

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1. Defining short-term outcomes of minor ischemic stroke due to small artery occlusion in the era of dual antiplatelet treatment: A READAPT study sub-analysis

2. Prevalence of Fabry disease and GLA variants in young patients with acute stroke: The challenge to widen the screening. The Fabry-Stroke Italian Registry

3. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

4. Divergence Between Clinical Trial Evidence and Actual Practice in Use of Dual Antiplatelet Therapy After Transient Ischemic Attack and Minor Stroke

6. Fabry-Stroke Italian Registry (FSIR): a nationwide, prospective, observational study about incidence and characteristics of Fabry-related stroke in young-adults. Presentation of the study protocol

8. Mitochondrial epilepsy: a cross-sectional nationwide Italian survey

9. Contributors

11. Primary Coenzyme Q10 Deficiency-Related Ataxias.

13. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

14. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

15. “Mitochondrial neuropathies”: A survey from the large cohort of the Italian Network

16. Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey

19. Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey

21. Redefining phenotypes associated with mitochondrial DNA single deletion

24. Mitochondrial DNA sequence variation and neurodegeneration

27. The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?

28. Fabry-Stroke Italian Registry (FSIR): a nationwide, prospective, observational study about incidence and characteristics of Fabry-related stroke in young-adults. Presentation of the study protocol

32. The Diagnostic Approach to Mitochondrial Disorders in Children in the Era of Next-Generation Sequencing: A 4-Year Cohort Study

33. Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases

39. Myoclonus in mitochondrial disorders

42. Electron transfer mediators and other metabolites and cofactors in the treatment of mitochondrial dysfunction

43. Increased Creatine Kinase May Predict A Worse COVID-19 Outcome

44. Mitochondrial Syndromes Revisited

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