Giovanni Antonini | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Impact of 2021 European Academy of Neurology/Peripheral Nerve Society diagnostic criteria on diagnosis and therapy of chronic inflammatory demyelinating polyradiculoneuropathy variants	EUROPEAN JOURNAL OF NEUROLOGY	2024
Assessment of diagnostic criteria for multifocal motor neuropathy in patients included in the Italian database	EUROPEAN JOURNAL OF NEUROLOGY	2024
Comprehensive Cardiovascular Management of Myotonic Dystrophy Type 1 Patients: A Report from the Italian Neuro-Cardiology Network	JOURNAL OF CARDIOVASCULAR DEVELOPMENT AND DISEASE	2024
Chronic inflammatory demyelinating polyneuropathy and HEV antibody status: A case-control study from Lazio, Italy	JOURNAL OF THE NEUROLOGICAL SCIENCES	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 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
Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutation	FRONTIERS IN NEUROLOGY	2023
Unclassified clinical presentations of chronic inflammatory demyelinating polyradiculoneuropathy	JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY	2023
Risk of disease relapse, safety and tolerability of SARS-CoV-2 vaccination in patients with chronic inflammatory neuropathies	EUROPEAN JOURNAL OF NEUROLOGY	2023
Safety and efficacy of rozanolixizumab in patients with generalised myasthenia gravis (MycarinG): a randomised, double-blind, placebo-controlled, adaptive phase 3 study	LANCET NEUROLOGY	2023
Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients	NEUROLOGICAL SCIENCES	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
Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis?	EUROPEAN JOURNAL OF NEUROLOGY	2023
Eculizumab for myasthenic exacerbation during treatment with immune-checkpoint inhibitors	NEUROLOGICAL SCIENCES	2023
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early- access program in Italy	EUROPEAN JOURNAL OF NEUROLOGY	2022
Functional and morphometric assessment of small-fibre damage in late-onset hereditary transthyretin amyloidosis with polyneuropathy: the controversial relation between small-fibre-related symptoms and diagnostic test findings	AMYLOID	2022
Muscle MRI in immune-mediated necrotizing myopathy (IMNM). implications for clinical management and treatment strategies	JOURNAL OF NEUROLOGY	2022
Distal upper limb involvement in myasthenia-myositis association	NEUROLOGICAL SCIENCES	2022
Nerve high-resolution ultrasound in a 2-years follow-up of radial nerve palsy related to humeral shaft fractures	JOURNAL OF NEUROSURGICAL SCIENCES	2022

Progetti di Ricerca

Hepatitis E Virus (HEV) infection and facial nerve palsy: a prospective study
RM muscolare nella Distrofia Miotonica di tipo 1 (DM1)
Identificazione di nuovi biomarcatori radiologici del danno muscolare nelle miopatie genetiche e acquisite
Valutazione dei disturbi dell'equilibrio mediante posturografia statica in pazienti affetti da Distrofia Miotonica di tipo 1 (DM1)