Search Results - "Vanoli, Fiammetta"

Muscle involvement in myasthenia gravis: Expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patients by Garibaldi, Matteo, Fionda, Laura, Vanoli, Fiammetta, Leonardi, Luca, Loreti, Simona, Bucci, Elisabetta, Di Pasquale, Antonella, Morino, Stefania, Vizzaccaro, Elisa, Merlonghi, Gioia, Ceccanti, Marco, Lucchini, Matteo, Mirabella, Massimiliano, Andreetta, Francesca, Pennisi, Elena Maria, Petrucci, Antonio, Salvetti, Marco, Antonini, Giovanni

“…Myastenia-Inflammatory Myopathy (MG-IM) association has been described in less than 50 cases, as isolated reports or in few case series. In most cases, MG and…”
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Changes of clinical, neurophysiological and nerve ultrasound characteristics in CIDP over time: a 3-year follow-up by Fionda, Laura, Di Pasquale, Antonella, Morino, Stefania, Leonardi, Luca, Vanoli, Fiammetta, Loreti, Simona, Garibaldi, Matteo, Lauletta, Antonio, Alfieri, Girolamo, Bucci, Elisabetta, Salvetti, Marco, Antonini, Giovanni

“…Objectives To evaluate, in a prospective study, high-resolution ultrasound (HRUS) changes of nerve segments in chronic inflammatory demyelinating…”
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Iatrogenic Kaposi’s sarcoma in myasthenia gravis: learnings from two case reports by Frangiamore, Rita, Giossi, Riccardo, Vanoli, Fiammetta, Tourlaki, Athanasia, Brambilla, Lucia, Maggi, Lorenzo, Mantegazza, Renato

“…Introduction Myasthenia gravis (MG) is an autoimmune neuromuscular disease whose treatment encompasses acetylcholinesterase inhibitors, oral steroids, and…”
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Skin biopsy and quantitative sensory assessment in an Italian cohort of ATTRv patients with polyneuropathy and asymptomatic carriers: possible evidence of early non-length dependent denervation by Leonardi, Luca, Galosi, Eleonora, Vanoli, Fiammetta, Fasolino, Alessandra, Di Pietro, Giuseppe, Luigetti, Marco, Sabatelli, Mario, Fionda, Laura, Garibaldi, Matteo, Alfieri, Girolamo, Lauletta, Antonio, Morino, Stefania, Salvetti, Marco, Truini, Andrea, Antonini, Giovanni

“…Aim Study of intraepidermal nerve fiber density (IENFD) by skin biopsy represents a promising tool in the evaluation of patients with ATTRv polyneuropathy…”
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Nerve ultrasonography findings as possible pitfall in differential diagnosis between hereditary transthyretin amyloidosis with polyneuropathy and chronic inflammatory demyelinating polyneuropathy by Leonardi, Luca, Vanoli, Fiammetta, Fionda, Laura, Loreti, Simona, Garibaldi, Matteo, Morino, Stefania, Salvetti, Marco, Russo, Domitilla, Musumeci, Beatrice, Antonini, Giovanni

“…Hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN) is a rare form of treatable severe progressive sensory-motor and autonomic polyneuropathy…”
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Complement Inhibition for the Treatment of Myasthenia Gravis by Mantegazza, Renato, Vanoli, Fiammetta, Frangiamore, Rita, Cavalcante, Paola

“…Generalized myasthenia gravis (gMG) is a rare autoimmune disorder affecting the neuromuscular junction (NMJ). Approximately 80-90% of patients display…”
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High-resolution ultrasound of peripheral nerves in late-onset hereditary transthyretin amyloidosis with polyneuropathy: similarities and differences with CIDP by Leonardi, Luca, Di Pietro, Giuseppe, Di Pasquale, Antonella, Vanoli, Fiammetta, Fionda, Laura, Garibaldi, Matteo, Galosi, Eleonora, Alfieri, Girolamo, Lauletta, Antonio, Morino, Stefania, Salvetti, Marco, Truini, Andrea, Antonini, Giovanni

“…Introduction Hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN) remains a diagnostic challenge due to clinical, neurophysiological, and…”
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Complement Activation Profile in Myasthenia Gravis Patients: Perspectives for Tailoring Anti-Complement Therapy by Iacomino, Nicola, Vanoli, Fiammetta, Frangiamore, Rita, Ballardini, Marta, Scandiffio, Letizia, Bortone, Federica, Andreetta, Francesca, Baggi, Fulvio, Bernasconi, Pia, Antozzi, Carlo, Cavalcante, Paola, Mantegazza, Renato

“…The complement system plays a key role in myasthenia gravis (MG). Anti-complement drugs are emerging as effective therapies to treat anti-acetylcholine…”
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Current drug treatment of myasthenia gravis by Vanoli, Fiammetta, Mantegazza, Renato

“…Purpose of review Myasthenia Gravis (MG) is a rare neurological disorder affecting the neuromuscular junction. Clinical hallmarks are fatigability and weakness…”
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Antibody Therapies in Autoimmune Neuromuscular Junction Disorders: Approach to Myasthenic Crisis and Chronic Management by Vanoli, Fiammetta, Mantegazza, Renato

“…Summary Myasthenia gravis (MG) is a neurological autoimmune disorder characterized by muscle weakness and fatigue. It is a B cell–mediated disease caused by…”
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Ravulizumab for the treatment of myasthenia gravis by Vanoli, Fiammetta, Mantegazza, Renato

“…Myasthenia gravis (MG) is a neurological B-cell mediated autoimmune disorder affecting the neuromuscular junction. MG therapeutics have always relied on…”
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What are the pharmacotherapeutic considerations for the treatment of myasthenia gravis? by Vanoli, Fiammetta, Mantegazza, Renato

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Reply to: intravenous immunoglobulin (Gamunex® 10%) is licensed for the treatment of severe acute exacerbations of myasthenia gravis by Vanoli, Fiammetta, Mantegazza, Renato

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miRNA in spinal muscular atrophy pathogenesis and therapy by Magri, Francesca, Vanoli, Fiammetta, Corti, Stefania

“…Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by the selective death of lower motor neurons in the brain stem…”
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Efgartigimod improves triple-negative myasthenia gravis by Frangiamore, Rita, Rinaldi, Elena, Vanoli, Fiammetta, Andreetta, Francesca, Mantegazza, Renato, Antozzi, Carlo

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mi RNA in spinal muscular atrophy pathogenesis and therapy by Magri, Francesca, Vanoli, Fiammetta, Corti, Stefania

“…Abstract Spinal muscular atrophy ( SMA ) is an autosomal recessive neurodegenerative disease characterized by the selective death of lower motor neurons in the…”
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Efgartigimod in generalized myasthenia gravis: A real‐life experience at a national reference center by Frangiamore, Rita, Rinaldi, Elena, Vanoli, Fiammetta, Andreetta, Francesca, Ciusani, Emilio, Bonanno, Silvia, Maggi, Lorenzo, Gallone, Annamaria, Colasuonno, Anna, Tramacere, Irene, Cheli, Marta, Pinna, Alessandro, Mantegazza, Renato, Antozzi, Carlo

“…Background and purpose Inhibition of the neonatal Fc receptor (FcRn) for IgG is a promising new therapeutic strategy for antibody‐mediated disorders. We report…”
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Concordance between patient‐ and physician‐reported Myasthenia Gravis Activities of Daily Living (MG‐ADL) scores by Dewilde, Sarah, Janssen, M. F., Tollenaar, Nafthali H., Vanoli, Fiammetta, Frangiamore, Rita, Phillips, Glenn, Paci, Sandra, Mantegazza, Renato, Meisel, Andreas, Stascheit, Frauke

“…Introduction/Aims Myasthenia gravis (MG) is a neuromuscular disease characterized by abnormal skeletal muscle fatiguability. The MG Activities of Daily Living…”
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Clinical and molecular features and therapeutic perspectives of spinal muscular atrophy with respiratory distress type 1 by Vanoli, Fiammetta, Rinchetti, Paola, Porro, Francesca, Parente, Valeria, Corti, Stefania

“…Spinal muscular atrophy with respiratory distress (SMARD1) is an autosomal recessive neuromuscular disease caused by mutations in the IGHMBP2 gene, encoding…”
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Muscle MRI in immune-mediated necrotizing myopathy (IMNM): implications for clinical management and treatment strategies by Fionda, Laura, Lauletta, Antonio, Leonardi, Luca, Perez, Jorge Alonso, Morino, Stefania, Merlonghi, Gioia, Alfieri, Girolamo, Costanzo, Rocco, Tufano, Laura, Vanoli, Fiammetta, Rossini, Elena, Vigo, Eduard Gallardo, Tartaglione, Tommaso, Salvetti, Marco, Antonini, Giovanni, Diaz-Manera, Jordi, Garibaldi, Matteo

“…Objectives Immune-mediated necrotizing myopathy (IMNM) is the most severe idiopathic inflammatory myopathy (IIM) and early aggressive poly-immunotherapy is…”
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