Marco Ceccanti

Pubblicazioni

Titolo Pubblicato in Anno
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
Emotion recognition in amyotrophic lateral sclerosis in a dynamic environment JOURNAL OF THE NEUROLOGICAL SCIENCES 2024
Metodologia clinica ragionata 2024
Oxidative Stress in Transthyretin-Mediated Amyloidosis: An Exploratory Study ANTIOXIDANTS 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
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
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
RNA Interference and Neuromuscular Diseases: A Focus on Hereditary Transthyretin Amyloidosis CURRENT GENE THERAPY 2023
Prominent mitochondrial pathology in a case of refractory dermatomyositis: coincidence or concause? NEUROLOGICAL SCIENCES 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
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

ERC

  • LS5
  • LS5_11

Keywords

amyotrophic lateral sclerosis
neuromuscular disease
amyloidosis

Progetti di Ricerca

Gruppi di ricerca

Gruppo di ricerca sulla sclerosi laterale amiotrofica
Gruppo di ricerca sull'amiloidosi sistemica da transtiretina

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