Matteo Garibaldi | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Comprehensive Cardiovascular Management of Myotonic Dystrophy Type 1 Patients: A Report from the Italian Neuro-Cardiology Network	JOURNAL OF CARDIOVASCULAR DEVELOPMENT AND DISEASE	2024
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease	BRAIN	2024
MiR206 and 423‑3p Are Differently Modulated in Fast and Slow‑Progressing Amyotrophic Lateral Sclerosis Patients	NEUROMOLECULAR MEDICINE	2024
Serum neurofilament light chain levels correlate with small fiber related parameters in patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN)	NEUROLOGICAL SCIENCES	2024
Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literature	ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY	2024
Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal study	JOURNAL OF NEUROLOGY	2024
Clinical, histopathologic, and genetic features of patients with myofibrillary and distal myopathies	NEUROLOGY	2024
Oxidative Stress in Transthyretin-Mediated Amyloidosis: An Exploratory Study	ANTIOXIDANTS	2024
Clinical Course of Neurologic Adverse Events Associated With Immune Checkpoint Inhibitors Focus on Chronic Toxicities	NEUROLOGY® NEUROIMMUNOLOGY & NEUROINFLAMMATION	2024
Management of overlapping immune-related myocarditis, myositis, and myasthenia in a young patient with advanced NSCLC: a case report	FRONTIERS IN ONCOLOGY	2024
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients	CLINICAL EPIGENETICS	2024
Effects of Triheptanoin on Mitochondrial Respiration and Glycolysis in Cultured Fibroblasts from Neutral Lipid Storage Disease Type M (NLSD-M) Patients	BIOMOLECULES	2023
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies. An Italian Nationwide Survey	NEUROLOGY	2023
NEFL-RELATED CHARCOT-MARIE TOOTH DISEASE DUE TO P440L MUTATION IN TWO ITALIAN FAMILIES: EXPANDING THE PHENOTYPE AND DEFINING MODULATING FACTORS	EUROPEAN NEUROLOGY	2023
Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients	NEUROLOGICAL SCIENCES	2023
Does Patisiran Reduce Ocular Transthyretin Synthesis? A Pilot Study of Two Cases	CURRENT NEUROPHARMACOLOGY	2023
Quantitative sensory testing and skin biopsy findings in late‐onset ATTRv pre‐symptomatic carriers: relationships with predicted time of disease onset (PADO)	JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM	2023
Prominent mitochondrial pathology in a case of refractory dermatomyositis: coincidence or concause?	NEUROLOGICAL SCIENCES	2023
Eculizumab for myasthenic exacerbation during treatment with immune-checkpoint inhibitors	NEUROLOGICAL SCIENCES	2023
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable?	ANNALS OF NEUROLOGY	2023

Progetti di Ricerca

Muscle pathology in Immune Mediated Necrotizing Myopathy (IMNM): implications for diagnostic accuracy and treatment strategies