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matteo.garibaldi@uniroma1.it
Matteo Garibaldi
Ricercatore
Struttura:
DIPARTIMENTO DI NEUROSCIENZE, SALUTE MENTALE E ORGANI DI SENSO
E-mail:
matteo.garibaldi@uniroma1.it
Pagina istituzionale corsi di laurea
Curriculum Sapienza
Publications
Title
Published on
Year
High-resolution ultrasound of peripheral nerves in late-onset hereditary transthyretin amyloidosis with polyneuropathy: similarities and differences with CIDP
NEUROLOGICAL SCIENCES
2021
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials
EUROPEAN JOURNAL OF NEUROLOGY
2021
Immune-mediated necrotizing myopathy (IMNM): a myopathological challenge
AUTOIMMUNITY REVIEWS
2021
Eculizumab in refractory generalized myasthenia gravis previously treated with rituximab: subgroup analysis of REGAIN and its extension study
MUSCLE & NERVE
2021
Creatine kinase and progression rate in amyotrophic lateral sclerosis
CELLS
2020
Muscle involvement in myasthenia gravis: Expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patients
AUTOIMMUNITY REVIEWS
2020
Immune checkpoint inhibitors (ICIs)-related ocular myositis
NEUROMUSCULAR DISORDERS
2020
Minimal Symptom Expression' in Patients With Acetylcholine Receptor Antibody-Positive Refractory Generalized Myasthenia Gravis Treated With Eculizumab
JOURNAL OF NEUROLOGY
2020
Telemedicine for neuromuscular disorders during the COVID-19 outbreak
JOURNAL OF NEUROLOGY
2020
Consistent improvement with eculizumab across muscle groups in myasthenia gravis
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY
2020
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy
BRAIN (ONLINE)
2020
Nerve ultrasonography findings as possible pitfall in differential diagnosis between hereditary transthyretin amyloidosis with polyneuropathy and chronic inflammatory demyelinating polyneuropathy
NEUROLOGICAL SCIENCES
2020
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores
NEUROMUSCULAR DISORDERS
2020
Gender effect on cardiac involvement in myotonic dystrophy type 1
EUROPEAN JOURNAL OF NEUROLOGY
2020
Nerve high resolution ultrasonography in Tangier disease
MUSCLE & NERVE
2019
Expanding the spectrum of genes responsible for hereditary motor neuropathies
JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY
2019
Nerve high-resolution ultrasonography in peripheral nerve injuries associated with supracondylar humeral fractures in children
JOURNAL OF CLINICAL NEUROSCIENCE
2019
Reply to the letter entitled “Predictors of respiratory impairment in patients with myotonic dystrophy type 1”
JOURNAL OF THE NEUROLOGICAL SCIENCES
2019
Eculizumab improves fatigue in refractory generalized myasthenia gravis
QUALITY OF LIFE RESEARCH
2019
Long-term safety and efficacy of eculizumab in generalized myasthenia gravis
MUSCLE & NERVE
2019
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Progetti di Ricerca
Muscle pathology in Immune Mediated Necrotizing Myopathy (IMNM): implications for diagnostic accuracy and treatment strategies
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