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7. Downregulation of exosomal miR-204-5p and miR-632 as a biomarker for FTD: a GENFI study

10. The Role of Amide Proton Transfer (APT)-Weighted Imaging in Glioma: Assessment of Tumor Grading, Molecular Profile and Survival in Different Tumor Components.

11. Bilateral Simultaneous Magnetic Resonance–Guided Focused Ultrasound Pallidotomy for Life‐Threatening Status Dystonicus.

13. Distinct neural signatures of pulvinar in C9orf72 amyotrophic lateral sclerosis mutation carriers and noncarriers

14. Focused ultrasound therapy in movement disorders: management roadmap toward optimal pathway organization

15. Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study

17. Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohort

18. Resting‐state fMRI functional connectome of C9orf72 mutation status

19. Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study.

20. Ambroxol as a disease-modifying treatment to reduce the risk of cognitive impairment inGBA-associated Parkinson’s disease: a multicentre, randomised, double-blind, placebo-controlled, phase II trial. The AMBITIOUS study protocol

22. Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study

23. Pain related to MRgFUS: a merely minor transient adverse event?

24. Aceruloplasminemia: Unique Clinical and MRI Findings in a Patient with a Novel Frameshift Mutation.

26. The optimal targeting for focused ultrasound thalamotomy differs between dystonic and essential tremor. A 12‐month prospective pilot study

27. White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort

28. Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene

29. A discriminative event-based model for subtype diagnosis of sporadic Creutzfeldt-Jakob disease using brain MRI

30. Letter to the editor: A case of functional isolated tongue tremor-like dyskinesia after COVID-19 vaccine

31. Complex Ataxia‐Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar Ataxia

32. A discriminative event‐based model for subtype diagnosis of sporadic Creutzfeldt‐Jakob disease using brain MRI

33. Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis

37. D14 Plasma levels of 24S-hydroxycholesterol are reduced in Huntington disease subjects: preliminary results of a 2-year longitudinal study

38. Magnetic Resonance–Guided Focused Ultrasound Thalamotomy May Spare Dopaminergic Therapy in Early‐Stage Tremor‐Dominant Parkinson's Disease: A Pilot Study

39. Comparison of arterial spin labeling registration strategies in the multi‐center GENetic frontotemporal dementia initiative (GENFI)

41. Degenerative Diseases

42. Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

45. Fotemustine in recurrent high‑grade glioma: MRI neuro‑radiological findings.

46. Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6

47. Pain related to MRgFUS: a merely minor transient adverse event?

49. Spinocerebellar Ataxia Type 1: One-Year Longitudinal Study to Identify Clinical and MRI Measures of Disease Progression in Patients and Presymptomatic Carriers

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