ArticleBrain sciences2020
hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers.
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Article in Brain sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.
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29citing papers in PubMed
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29 citing papers in PubMed, 41 citations in OpenAlex.
- Longitudinal multimodal assessment of peripheral nerve involvement in wild-type transthyretin amyloidosis.Journal of neurology · 2026Article
- p. His110Asn: confirmation of pathological ATTRv variant.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026Article
- Clinical and genetic features of hereditary transthyretin amyloidosis with polyneuropathy in China: insights from case analysis and literature review.Frontiers in genetics · 2026Article
- The Vagal Link: Autonomic Nervous System Dysfunction in Cardiac Amyloidosis.Journal of clinical medicine · 2025Review
- Atypical gastrointestinal presentation of hereditary transthyretin amyloidosis: a case report highlighting the diagnostic challenge.European heart journal. Case reports · 2025Article
- Polyneuropathy in Wild-Type Transthyretin Amyloidosis.European journal of neurology · 2025Article
- Comparative Analysis of SiMoA and Ella Immunoassay Platforms for Measuring Serum Neurofilament Light Chain Levels in ATTRv With Polyneuropathy and Presymptomatic Carriers.European journal of neurology · 2025Article
- Basic Pathological Mechanisms in Peripheral Nerve Diseases.International journal of molecular sciences · 2025Review
- Cardiovascular and brain effects of liraglutide in transthyretin amyloidosis (ATTR) mice models.International journal of medical sciences · 2025Article
- Clinical differential factors in patients with hereditary transthyretin amyloidosis with Val142Ile and Ser43Asn mutations.Orphanet journal of rare diseases · 2024Article
- Global longitudinal strain in pre-symptomatic patients with mutation for transthyretin amyloidosis.Orphanet journal of rare diseases · 2024Article
- Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024Observational
- Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024Article
- Genetic screening for hereditary transthyretin amyloidosis with polyneuropathy in western Sicily: Two years of experience in a neurological clinic.European journal of neurology · 2024Article
- Machine Learning for Early Diagnosis of ATTRv Amyloidosis in Non-Endemic Areas: A Multicenter Study from Italy.Brain sciences · 2023Article
- Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features.Annals of clinical and translational neurology · 2023Article
- Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutation.Frontiers in neurology · 2023Article
- Quantitative Sensory Testing in Late-Onset ATTRv Presymptomatic Subjects: A Single Center Experience.Biomedicines · 2022Article
- Cutaneous amyloid is a biomarker in early ATTRv neuropathy and progresses across disease stages.Annals of clinical and translational neurology · 2022Article
- Nerve Conduction Studies of Dorsal Sural Nerve: Normative Data and Its Potential Application in ATTRv Pre-Symptomatic Subjects.Brain sciences · 2022Article
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Authors and funding
21 authors at 8 institutions in 1 country.
Marco LuigettiFondazione Policlinico Universitario A. Gemelli IRCCS, UOC Neurologia, 00168 Roma, Italy.ORCID 0000-0001-7539-505X
Marina RomozziFondazione Policlinico Universitario A. Gemelli IRCCS, UOC Neurologia, 00168 Roma, Italy.
Giulia BisogniCentro Clinico NEMO-Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
Davide CardelliniDipartimento di Neuroscienze, Biomedicina e Scienze del Movimento, Università di Verona, 37134 Verona, Italy.
Tiziana CavallaroDipartimento di Neuroscienze, Biomedicina e Scienze del Movimento, Università di Verona, 37134 Verona, Italy.
Andrea Di PaolantonioDipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
Gian Maria FabriziDipartimento di Neuroscienze, Biomedicina e Scienze del Movimento, Università di Verona, 37134 Verona, Italy.
Silvia FenuRare Neurodegenerative and Neurometabolic Diseases Unit, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.
Luca GentileDepartment of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.
Marina GrandisDipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno Infantili (DINOGMI), Università degli studi di Genova, 16132 Genova, Italy.
Gianluca MarucciNeuropathology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.ORCID 0000-0003-4508-3359
Sara MassuccoDipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno Infantili (DINOGMI), Università degli studi di Genova, 16132 Genova, Italy.
Anna MazzeoDepartment of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.
Davide PareysonRare Neurodegenerative and Neurometabolic Diseases Unit, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.ORCID 0000-0001-6854-765X
Angela RomanoDipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.ORCID 0000-0002-2061-1509
Massimo RussoDepartment of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.
Angelo SchenoneDipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno Infantili (DINOGMI), Università degli studi di Genova, 16132 Genova, Italy.ORCID 0000-0002-2604-7830
Matteo TagliapietraDipartimento di Neuroscienze, Biomedicina e Scienze del Movimento, Università di Verona, 37134 Verona, Italy.ORCID 0000-0002-3048-1453
Stefano TozzaDipartimento di Neuroscienze, Scienze della Riproduzione e Oftalmologiche, Università Federico II di Napoli, 80131 Napoli, Italy.ORCID 0000-0002-9672-4577
Giuseppe VitaDepartment of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.
Mario SabatelliDipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
Università Cattolica del Sacro Cuore · ITUniversity of Messina · ITUniversity of Verona · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITOspedale Policlinico San Martino · ITCentro Clinico Nemo · ITUniversity of Genoa · ITUniversity of Naples Federico II · IT
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pathological evidence of amyloid on nerve biopsy has been the gold standard for diagnosis in hereditary transthyretin amyloidosis polyneuropathy (hATTR-PN) for a long time. In this article, we reviewed the pathological findings of a large series of sural nerve biopsies from a cohort of hATTR-PN patients, collected by different Italian referral centers.
Indexed as
amyloidaxonal lossCongo redhATTRnerve biopsypolyneuropathy
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