658 results on '"Casali C"'
Search Results
2. Non-technical skills for neurosurgeons: An international survey
3. THE USE OF FAILURE MODE AND EFFECTS ANALYSIS FOR RISK ASSESSMENT (FMEA) IN LASER INTERSTITIAL THERMAL THERAPY (LITT)
4. The Working Life of People with Degenerative Cerebellar Ataxia
5. Locomotor coordination in patients with Hereditary Spastic Paraplegia
6. Treatment of Central Nervous System Involvement
7. Differential changes in the spinal segmental locomotor output in Hereditary Spastic Paraplegia
8. PC-05.4 - THE USE OF FAILURE MODE AND EFFECTS ANALYSIS FOR RISK ASSESSMENT (FMEA) IN LASER INTERSTITIAL THERMAL THERAPY (LITT)
9. Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A).
10. Altered TDP‐43‐dependent splicing in HSPB8‐related distal hereditary motor neuropathy and myofibrillar myopathy
11. Neuro-telehealth for fragile patients in a tertiary referral neurological institute during the COVID-19 pandemic in Milan, Lombardy
12. Advanced rehearsal for steeper the learning curve in skull base tumour (the ‘stars-ct-made’ study)
13. Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review (Journal of Neurology, (2021), 10.1007/s00415-021-10792-3)
14. ‘When atlastin meets spastin’
15. Allogeneic hematopoietic SCT as treatment option for patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a consensus conference proposal for a standardized approach
16. Large deletion mutation of SPAST in a multi-generation family from Sardinia
17. Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56
18. Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I–II loop
19. Multiple mtDNA deletions: Clinical and molecular correlations
20. Antioxidant enzymes in blood of patients with Friedreich's ataxia. (Original Article)
21. Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)
22. Myelinated retinal fibers in autosomal recessive spastic ataxia of Charlevoix-Saguenay
23. Allogeneic HSCT for mitochondrial neurogastrointestinal encephalomyopathy: the first promising effective treatment option in an otherwise unrelenting progressive disease?: O398
24. Impairment of global lower limb muscle coactivation during walking in cerebellar ataxias
25. SSEEM-An Innovative Spread Spectrum System For Satcom Antenna Radiation Pattems Measurements
26. A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy
27. BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson’s disease
28. Thymoma classification: does it matter?
29. Tuberous sclerosis complex presenting as a pulmonary solitary nodule
30. Preoperative localization of indeterminate pulmonary nodules before videothoracoscopic resection
31. Glutathione in blood of patients with Friedreichʼs ataxia
32. Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes
33. Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
34. RELATIONSHIP BETWEEN SOCIOECONOMIC FACTORS AND DELAY IN DIAGNOSIS AND INITIAL TREATMENT IN PATIENTS WITH DIFUSSE LARGE B CELL LYMPHOMA (DLBCL). DO THESE FACTORS IMPACT ON THE RESPONSE RATE? RESULTS OF A MULTICENTRIC ARGENTINIAN STUDY
35. High-resolution study of epigenetic processes: new insights into methylation and demethylation
36. 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] (S0268003317301389) (10.1016/j.clinbiomech.2017.07.001))
37. Non-technical skills for neurosurgeons: An international survey
38. Hereditäre spastische Spinalparalyse: türkische Familie mit Mutation im Spatacsin-Gen (SPG 11)
39. Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
40. Altered TDP-43-dependent splicing in HSPB8 -related distal hereditary motor neuropathy and myofibrillar myopathy
41. Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association
42. DISTRUZIONE DELLA CUSCUTA
43. Ochratoxin A and liver damage: a case-control study
44. Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy
45. Retrospective Multicenter Real-Life Study on the First-Line Treatment of Classical Hodgkin Lymphoma in Argentina
46. Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): The liver as a new source of thymidine phosphorylase
47. L’encefalomiopatia Mitocondriale Neurogastrointestinale (MNGIE): Il Fegato Come Nuova Fonte Di Timidina Fosforilasi
48. The Liver as a New Tissue Source of Thymidine Phosphorylase for Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE)
49. Infantile-onset Hereditary spastic paraplegia associated with SPAST mutations (SPG4): clinical and follow-up studies
50. A Novel CBFA1 mutation in an Italian family CCD with skeletal myopathy
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