Maurizio Inghilleri | 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
Chronic inflammatory demyelinating polyneuropathy and HEV antibody status: A case-control study from Lazio, Italy	JOURNAL OF THE NEUROLOGICAL SCIENCES	2024
MiR206 and 423‑3p Are Differently Modulated in Fast and Slow‑Progressing Amyotrophic Lateral Sclerosis Patients	NEUROMOLECULAR MEDICINE	2024
SMN deficiency destabilizes ABCA1 expression in human fibroblasts: novel insights in pathophysiology of spinal muscular atrophy	INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES	2023
Immune-mediated myogenesis and acetylcholine receptor clustering promote a slow disease progression in ALS mouse models	INFLAMMATION AND REGENERATION	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
Retrospective observational study on the use of acetyl-L-carnitine in ALS	JOURNAL OF NEUROLOGY	2023
Does Patisiran Reduce Ocular Transthyretin Synthesis? A Pilot Study of Two Cases	CURRENT NEUROPHARMACOLOGY	2023
Correction: Immune-mediated myogenesis and acetylcholine receptor clustering promote a slow disease progression in ALS mouse models	INFLAMMATION AND REGENERATION	2023
Withdrawal of mechanical ventilation in amyotrophic lateral sclerosis patients: a multicenter Italian survey	NEUROLOGICAL SCIENCES	2023
RNA Interference and Neuromuscular Diseases: A Focus on Hereditary Transthyretin Amyloidosis	CURRENT GENE THERAPY	2023
Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis?	EUROPEAN JOURNAL OF NEUROLOGY	2023
Genetics screening in an Italian cohort of patients with Amyotrophic Lateral Sclerosis: the importance of early testing and its implication	JOURNAL OF NEUROLOGY	2023
A novel homozygous mutation in TBK1 gene causing ALS-FTD	NEUROLOGICAL SCIENCES	2022
Paraneoplastic neuromyelitis optica spectrum disorder associated with lung adenocarcinoma: a case report	FRONTIERS IN MEDICINE	2022
Classical and Unexpected Effects of Ultra-Micronized {PEA} in Neuromuscular Function	BIOMOLECULES	2022
Effects of Skin Stimulation on Sensory-Motor Networks Excitability: Possible Implications for Physical Training in Amyotrophic Lateral Sclerosis	FRONTIERS IN NEUROLOGY	2022
The Silent Period for Small Fiber Sensory Neuropathy Assessment in a Mixed Cohort of Transthyretin-Mediated Amyloidosis	BIOMEDICINES	2022

Gruppi di ricerca - Responsabile

Gruppo di ricerca sulla sclerosi laterale amiotrofica

Gruppo di ricerca sull'amiloidosi sistemica da transtiretina

Laboratori di ricerca

LABORATORIO DI MALATTIE NEUROMUSCOLARI RARE