42 results on '"Marcotulli, Christian"'
Search Results
2. Identification of specific gait patterns in patients with cerebellar ataxia, spastic paraplegia, and Parkinson’s disease: A non-hierarchical cluster analysis
3. 15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias
4. Cortical sources of resting state electroencephalographic rhythms differ in relapsing–remitting and secondary progressive multiple sclerosis
5. Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial
6. Progression of Gait Ataxia in Patients with Degenerative Cerebellar Disorders: a 4-Year Follow-Up Study
7. A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study
8. Retinal and Visual Pathways Involvement in Carriers of Friedreich’s Ataxia
9. GIFT-1, a phase IIa clinical trial to test the safety and efficacy of IFNγ administration in FRDA patients
10. Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 family
11. A Clinical and Epidemiological Prevalence Study on Friedreich's Ataxia in Latium, Italy
12. Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease
13. Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1
14. Long-term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia
15. Acute optic neuropathy associated with a novel MFN2 mutation
16. Hsa-miR223-3p circulating level is upregulated in Friedreich’s ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1
17. A Clinical and Epidemiological Prevalence Study on Friedreich’s Ataxia in Latium, Italy
18. Cerebellum and neuropsychiatric disorders: insights from ARSACS
19. Safety and feasibility of upper limb cardiopulmonary exercise test in Friedreich ataxia
20. De novo mutations in SPG3A: a challenge in differential diagnosis and genetic counselling
21. Safety and feasibility of upper limb cardiopulmonary exercise test in Friedreich ataxia.
22. Early-onset optic neuropathy as initial clinical presentation in SPG7
23. Developing an objective evaluating system to quantify the degree of upper limb movement impairment in patients with severe Friedreich’s ataxia
24. Frataxin deficiency in Friedreich’s ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survival
25. Analisi del cammino nelle atassie cerebellari degenerative
26. Developing a smartphone application, triaxial accelerometer-based, to quantify static and dynamic balance deficits in patients with cerebellar ataxias
27. Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
28. Dataset on gait patterns in degenerative neurological diseases
29. Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
30. A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study
31. Progression of Gait Ataxia in Patients with Degenerative Cerebellar Disorders: a 4-Year Follow-Up Study
32. Long-Term Effect of Epoetin Alfa on Clinical and Biochemical Markers in Friedreich Ataxia (P5.387)
33. 'When atlastin meets spastin'
34. Spinocerebellar Ataxia Type 3 in Italy: Time to Change Mind
35. GIFT-1, a phase IIa clinical trial to test the safety and efficacy of IFNγ administration in FRDA patients
36. Cerebellum and neuropsychiatric disorders: insights from ARSACS
37. Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1.
38. Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/ CYP2U1 family.
39. Safety and feasibility of upper limb cardiopulmonary exercise test in Friedreich ataxia
40. Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
41. A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias. A pilot open-labeled study
42. Dataset on gait patterns in degenerative neurological diseases.
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