1,378 results on '"LIGUORI, ROCCO"'
Search Results
2. Therapeutic challenges and unmet needs in the management of myasthenia gravis: an Italian expert opinion
3. Two more families supporting the existence of monogenic spinocerebellar ataxia 48
4. Bibrachial amyotrophy as a rare manifestation of intraspinal fluid collection: a case report and systematic review
5. Fabry disease in W162C mutation: a case report of two patients and a review of literature
6. Comparative assessment of MScanFit MUNE and quantitative EMG in amyotrophic lateral sclerosis diagnosis: A prospective study
7. Volumetric absorptive microsampling coupled with UHPLC-MS/MS for the determination of Lyso-Gb3 as Fabry disease diagnostic biomarker
8. Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional study
9. Effect of tauroursodeoxycholic acid on survival and safety in amyotrophic lateral sclerosis: a retrospective population-based cohort study
10. Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?
11. Late-onset Fabry disease due to a new (p.Pro380Leu) pathogenic variant of GLA Gene
12. Anti-LGI1 encephalitis following COVID-19 vaccination: a case series
13. Cannabinoids for painful dystonia in corticobasal syndrome: a report of three patients
14. Chromatic Pupillometry Findings in Alzheimers Disease.
15. Clinical characteristics of a large cohort of patients with narcolepsy candidate for pitolisant: a cross-sectional study from the Italian PASS Wakix® Cohort
16. GABAA receptor and anti-titin antibody encephalitis in a patient with thymoma
17. Multiple sclerosis in patients with hereditary spastic paraplegia: a case report and systematic review
18. Difference in safety and humoral response to mRNA SARS-CoV-2 vaccines in patients with autoimmune neurological disorders: the ANCOVAX study
19. Pathology vs pathogenesis: Rationale and pitfalls in the clinicopathology model of neurodegeneration
20. Cognitive and functional connectivity impairment in post-COVID-19 olfactory dysfunction
21. Fabry Disease Nephropathy: Histological Changes With Nonclassical Mutations and Genetic Variants of Unknown Significance
22. The role of antibodies in small fiber neuropathy: a review of currently available evidence
23. Clinical, prognostic and pathophysiological implications of MOG-IgG detection in the CSF: the importance of intrathecal MOG-IgG synthesis
24. Quality of life assessment in adult spinal muscular atrophy patients treated with nusinersen
25. Pilomotor seizures in autoimmune limbic encephalitis: description of two GAD65 antibodies- related cases and literature review
26. Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study
27. Self-Induced Stretch Syncope: An Unusual Non-Epileptic Paroxysmal Event. A Case Report and Literature Mini-Review.
28. Co‐occurrence of glial fibrillary acidic protein astrocytopathy in a patient with Leber's hereditary optic neuropathy due to DNAJC30 mutations.
29. Motor unit number estimation via MScanFit MUNE in spinal muscular atrophy
30. Seeding Activity of Skin Misfolded Tau as a Biomarker for Tauopathies
31. HLA-DQB1*05 subtypes and not DRB1*10:01 mediates risk in anti-IgLON5 disease
32. Biomarkers of neurodegeneration in isolated and antidepressant‐related rapid eye movement sleep behavior disorder
33. The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypes
34. Antibodies to neuronal surface antigens in patients with a clinical diagnosis of neurodegenerative disorder
35. Intravenous immunoglobulin therapy in COVID-19-related encephalopathy
36. Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients
37. A Second Case With the V374A KCND3 Pathogenic Variant in an Italian Patient With Early-Onset Spinocerebellar Ataxia
38. Comparison of 123I-MIBG scintigraphy and phosphorylated α-synuclein skin deposits in synucleinopathies
39. Benefit and danger from immunotherapy in myasthenia gravis
40. FADD gene pathogenic variants causing recurrent febrile infection‐related epilepsy syndrome: Case report and literature review.
41. Sulcal Morphometry Predicts Mild Cognitive Impairment Conversion to Alzheimer's Disease.
42. Primary Lateral Sclerosis: An Overview
43. Melanopsin retinal ganglion cell loss in Alzheimer disease
44. The genetic puzzle of a SOD1-patient with ocular ptosis and a motor neuron disease: a case report
45. Progressive Ataxia and Palatal Tremor Is Not Associated with IgLON5 Antibodies: Results From Two Cases
46. Correlations Between Cardiac Magnetic Resonance and Myocardial Histologic Findings in Fabry Disease
47. Bibrachial amyotrophy as a rare manifestation of intraspinal fluid collection: a case report and systematic review
48. Effect of tauroursodeoxycholic acid on survival and safety in amyotrophic lateral sclerosis: a retrospective population-based cohort study
49. Multiple intra‐axial lesions in a 57‐year‐old male with a history of B‐cell chronic lymphocytic leukemia.
50. Sensitivity and specificity of single-fibre EMG in the diagnosis of ocular myasthenia varies accordingly to clinical presentation
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