614 results on '"Casali, Carlo"'
Search Results
2. Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort
3. Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variability
4. Local Dynamic Stability of Trunk During Gait is Responsive to Rehabilitation in Subjects with Primary Degenerative Cerebellar Ataxia
5. Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
6. Correction to: Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort
7. A Delphi consensus to identify the key screening tests/questions for a digital neurological examination for epidemiological research
8. Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature
9. Consensus Paper: Ataxic Gait
10. Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice
11. Identification of Gait Unbalance and Fallers Among Subjects with Cerebellar Ataxia by a Set of Trunk Acceleration-Derived Indices of Gait
12. Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias
13. Correction to: Consensus Paper: Ataxic Gait
14. Imaging-based methods to identify prognostic and predictive biomarkers for Hereditary Spastic Paraplegia
15. Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations
16. Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
17. Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
18. The VDR FokI (rs2228570) polymorphism is involved in Parkinson's disease
19. Reversible conduction block of peroneal nerve associated with SARS-CoV-2
20. The Effect of a Wearable Assistive Trunk Exoskeleton on the Motor Coordination of People with Cerebellar Ataxia.
21. Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
22. Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study
23. Comprehensive Cardiovascular Management of Myotonic Dystrophy Type 1 Patients: A Report from the Italian Neuro-Cardiology Network
24. Liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical long-term follow-up and pathogenic implications
25. Impairment of Global Lower Limb Muscle Coactivation During Walking in Cerebellar Ataxias
26. Developing a smartphone application, triaxial accelerometer-based, to quantify static and dynamic balance deficits in patients with cerebellar ataxias
27. Optimizing Rare Disease Gait Classification through Data Balancing and Generative AI: Insights from Hereditary Cerebellar Ataxia.
28. TNF-α − 308 G/A and − 238 G/A promoter polymorphisms and sporadic Parkinson's disease in an Italian cohort
29. Identification of specific gait patterns in patients with cerebellar ataxia, spastic paraplegia, and Parkinson’s disease: A non-hierarchical cluster analysis
30. 15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias
31. SNAP25 Gene Polymorphisms Protect Against Parkinson’s Disease and Modulate Disease Severity in Patients
32. Roussy-Lévy syndrome: a case of genotype–phenotype correlation
33. Increased lower limb muscle coactivation reduces gait performance and increases metabolic cost in patients with hereditary spastic paraparesis
34. Harmony as a convergence attractor that minimizes the energy expenditure and variability in physiological gait and the loss of harmony in cerebellar ataxia
35. Trunk-lower limb coordination pattern during gait in patients with ataxia
36. Long term clinical and neurophysiological effects of cerebellar transcranial direct current stimulation in patients with neurodegenerative ataxia
37. Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
38. N°134 – Nerve ultrasound findings in Friedreich’s Ataxia
39. New cellular imaging‐based method to distinguish SPG4 subtype of Hereditary Spastic Paraplegia
40. Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial
41. Progression of Gait Ataxia in Patients with Degenerative Cerebellar Disorders: a 4-Year Follow-Up Study
42. A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study
43. Local Stability of the Trunk in Patients with Degenerative Cerebellar Ataxia During Walking
44. Use of Dynamic Movement Orthoses as Rehabilitative Method to Improve Gait Stability in Ataxic Patients
45. Retinal and Visual Pathways Involvement in Carriers of Friedreich’s Ataxia
46. Neurophysiology of gait
47. Consensus Paper: Revisiting the Symptoms and Signs of Cerebellar Syndrome
48. GIFT-1, a phase IIa clinical trial to test the safety and efficacy of IFNγ administration in FRDA patients
49. Oculomotor deficits affect neuropsychological performance in oculomotor apraxia type 2
50. Corrigendum to “Harmony as a convergence attractor that minimizes the energy expenditure and variability in physiological gait and the loss of harmony in cerebellar ataxia.”[Clin. Biomech. 48 (2017) 15-23]
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