342 results on '"Monforte, Mauro"'
Search Results
2. Correction to: Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP‑mediated disease reveals characteristic features useful for diagnosis
3. Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis
4. Myo-regressor Deep Informed Neural NetwOrk (Myo-DINO) for fast MR parameters mapping in neuromuscular disorders
5. Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort study
6. Muscle magnetic resonance imaging of a large cohort of distal hereditary motor neuropathies reveals characteristic features useful for diagnosis
7. Large vessel stroke and isolated thrombocytopenia as presenting features of thrombotic thrombocytopenic purpura
8. Artificial intelligence to predict individualized outcome of acute ischemic stroke patients: The SIBILLA project
9. Deep learning for automatic segmentation of thigh and leg muscles
10. Diagnostic magnetic resonance imaging biomarkers for facioscapulohumeral muscular dystrophy identified by machine learning
11. Dynamic magnetic resonance imaging of muscle contraction in facioscapulohumeral muscular dystrophy
12. Anton syndrome
13. Baseline clinical and neuroradiological predictors of outcome in patients with large ischemic core undergoing mechanical thrombectomy: A retrospective multicenter study.
14. Muscle diffusion tensor imaging in facioscapulohumeral muscular dystrophy.
15. Movement disorders following mechanical thrombectomy resulting in ischemic lesions of the basal ganglia: An emerging clinical entity
16. Hospital admissions from the emergency department of adult patients affected by myopathies
17. Effect of the COVID-19 pandemic and the lockdown measures on the local stroke network
18. Automated Pupillometry Is Able to Discriminate Patients with Acute Stroke from Healthy Subjects: An Observational, Cross-Sectional Study.
19. Stroke-related delirium in patients undergoing revascularization treatments: A retrospective, observational study
20. Prolonged Secondary Stroke Prevention with Edoxaban: A Long-Term Follow-Up of the SATES Study
21. Meeting report: The 2023 FSHD International Research Congress
22. The administration of antisense oligonucleotide golodirsen reduces pathological regeneration in patients with Duchenne muscular dystrophy
23. European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A)
24. Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD
25. Clinical Classification of Variants in the Valosin-Containing Protein Gene Associated With Multisystem Proteinopathy
26. Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy
27. Clinical Reasoning: A 71-Year-Old Man Presenting With Acute Onset Dysarthria and Dysphagia
28. Muscle Microdialysis to Investigate Inflammatory Biomarkers in Facioscapulohumeral Muscular Dystrophy
29. Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort
30. Artificial Intelligence for Evaluation of Retinal Vasculopathy in Facioscapulohumeral Dystrophy Using OCT Angiography: A Case Series
31. Radiomics and machine learning applied to STIR sequence for prediction of quantitative parameters in facioscapulohumeral disease
32. 265th ENMC International Workshop: Muscle imaging in Facioscapulohumeral Muscular Dystrophy (FSHD): relevance for clinical trials. 22–24 April 2022, Hoofddorp, The Netherlands
33. Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1
34. D4Z4 Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients
35. Large vessel stroke and isolated thrombocytopenia as presenting features of thrombotic thrombocytopenic purpura
36. COVID-19 Vaccination Is Associated with a Better Outcome in Acute Ischemic Stroke Patients: A Retrospective Observational Study
37. Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey
38. Anton syndrome
39. Contrast-induced Encephalopathy
40. Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy
41. Congenital Left Ventricular Diverticulum: A Rare Cause of Recurrent Juvenile Cryptogenic Stroke
42. MRI in sarcoglycanopathies: a large international cohort study
43. Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey
44. Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods
45. Muscle MRI in Becker muscular dystrophy
46. New phenotype and pathology features in MYH7-related distal myopathy
47. Technology outcome measures in neuromuscular disorders: A systematic review
48. Effect of lockdown on the management of ischemic stroke: an Italian experience from a COVID hospital
49. Deep learning for automatic segmentation of thigh and leg muscles
50. Matrin 3 variants are frequent in Italian ALS patients
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