414 results on '"Cavallaro, Tiziana"'
Search Results
2. Correction to: Daytime sleepiness and sleep quality in Charcot–Marie–Tooth disease
3. Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry
4. Diabetic Neuropathy
5. Infectious Neuropathies
6. Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy
7. Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis
8. RFC1 AAGGG repeat expansion masquerading as Chronic Idiopathic Axonal Polyneuropathy
9. CIDP, CMT1B, or CMT1B plus CIDP?
10. Nerve ultrasound in hereditary transthyretin amyloidosis: red flags and possible progression biomarkers
11. Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology.
12. Use, tolerability, benefits and side effects of orthotic devices in Charcot-Marie-Tooth disease.
13. Sural nerve biopsy: current role and comparison with serum neurofilament light chain levels
14. Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs
15. Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study
16. P155/200 Usefulness of quadri-axial system in mechanical thrombectomy in acute ischemic stroke: redefining the boundaries of trans-femoral access
17. P020/203 First description of asymptomatic dissecting aneurysm arising from a perforating branch of posterior communicating artery: report of its unusual clinical presentation, evolution and endovascular treatment
18. Clinical and pathology characterization of small nerve fiber neuro(no)pathy in cerebellar ataxia with neuropathy and vestibular areflexia syndrome
19. The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study
20. Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I
21. Isolated leptomeningeal angiomatosis in the sixth decade of life, an adulthood variant of Sturge Weber Syndrome (Type III): role of advanced Magnetic Resonance Imaging and Digital Subtraction Angiography in diagnosis
22. Pregnancy in Charcot-Marie-Tooth disease: Data from the Italian CMT national registry
23. Infectious Neuropathies
24. Diabetic Neuropathy
25. Saposin B deficiency as a cause of adult-onset metachromatic leukodystrophy
26. Peripheral neuropathy as clinical onset of monoclonal IgM/k‐related amyloidosis
27. Clinical spectrum and frequency of Charcot–Marie–Tooth disease in Italy: Data from the National CMT Registry.
28. Polyneuropathy with anti-sulfatide and anti-MAG antibodies: Clinical, neurophysiological, pathological features and response to treatment
29. GRN−/− iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosis
30. Clinical and pathological findings in neurolymphomatosis: Preliminary association with gene expression profiles in sural nerves
31. Primary neurolymphomatosis as clinical onset of chronic lymphocytic leukemia
32. Magnetic resonance parkinsonism index in progressive supranuclear palsy and vascular parkinsonism
33. Frequency, entity and determinants of fatigue in Charcot–Marie–Tooth disease.
34. Neuroimaging in diagnosis of atypical polyradiculoneuropathies: report of three cases and review of the literature
35. Charcot–Marie–Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family
36. Neuropathic pain in Charcot–Marie‐Tooth disease: A clinical and laser‐evoked potential study
37. Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRI AAL and CMT-TRAUK): a double-blind randomised trial
38. Huffer’s neuropathy: A case of acute-onset tetraparesis mimicking Guillain-Barré syndrome
39. Clinical and pathological characterization of RFC1 AAGGG expansion presenting as chronic axonal polyneuropathy
40. Hereditary neuropathies: A pathological perspective
41. Featured Cover
42. Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis
43. A 58‐year‐old man with B‐cell chronic lymphocytic leukemia and multiple strokes
44. Multiple Mononeuropathy in Churg-Strauss Syndrome Presenting as a Subacute Ascending Polineuropathy: A Case Report
45. Atypical Alzheimer’s disease: a case report
46. Executive Dysfunctions in Migraine With and Without Aura: What Is the Role of White Matter Lesions?
47. Alpha-synuclein seeds in olfactory mucosa and cerebrospinal fluid of patients with dementia with Lewy bodies
48. Peripheral nerve enlargement on nerve ultrasound parallels neuropathological changes in adult‐onset Krabbe disease
49. Mechanisms of Nerve Damage in Neuropathies Associated with Hematological Diseases: Lesson from Nerve Biopsies
50. A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.