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

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

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

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

11. The Corticospinal Tract in Huntington's Disease

12. Evidence that hippocampal–parahippocampal dysfunction is related to genetic risk for schizophrenia

14. Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease

15. Validation of the Italian version of the PSP Quality of Life questionnaire

16. Curcumin dietary supplementation ameliorates disease phenotype in an animal model of Huntington's disease

17. Validation of the Italian version of carers’ quality-of-life questionnaire for parkinsonism (PQoL Carer) in progressive supranuclear palsy

18. No evidence of iron deposition in essential tremor: a susceptibility-weighted imaging study.

19. Validation of the Italian version of the PSP Quality of Life questionnaire.

20. White matter rather than gray matter damage characterizes essential tremor.

21. Validation of the Italian version of carers' quality-of-life questionnaire for parkinsonism (PQoL Carer) in progressive supranuclear palsy.

22. Author Correction: Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease.

23. Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease.

24. Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease.

25. Deep white matter in Huntington's disease.

26. Changes of peripheral TGF-β1 depend on monocytes-derived macrophages in Huntington disease.

27. Tractography of the corpus callosum in Huntington's disease.

28. Seeking Huntington disease biomarkers by multimodal, cross-sectional basal ganglia imaging.

29. 18F-FDG PET uptake in the pre-Huntington disease caudate affects the time-to-onset independently of CAG expansion size.

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