Serum neurofilament light chain levels correlate with small fiber related parameters in patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN)
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
-
Serum neurofilament light chain levels correlate with small fiber related parameters in patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN) ; day:3 ; month:5 ; year:2024 ; pages:1-10
Neurological sciences ; (3.5.2024), 1-10
- Creator
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Galosi, Eleonora
Costanzo, Rocco
Forcina, Francesca
Morino, Stefania
Antonini, Giovanni
Salvetti, Marco
Lauletta, Antonio
Luigetti, Marco
Romano, Angela
Primiano, Guido
Guglielmino, Valeria
Fionda, Laura
Garibaldi, Matteo
Esposito, Nicoletta
Falco, Pietro
Pietro, Giuseppe di
Truini, Andrea
Leonardi, Luca
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s10072-024-07562-0
- URN
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urn:nbn:de:101:1-2407142113307.520694799533
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:53 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Galosi, Eleonora
- Costanzo, Rocco
- Forcina, Francesca
- Morino, Stefania
- Antonini, Giovanni
- Salvetti, Marco
- Lauletta, Antonio
- Luigetti, Marco
- Romano, Angela
- Primiano, Guido
- Guglielmino, Valeria
- Fionda, Laura
- Garibaldi, Matteo
- Esposito, Nicoletta
- Falco, Pietro
- Pietro, Giuseppe di
- Truini, Andrea
- Leonardi, Luca
- SpringerLink (Online service)
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Evaluation of Mortality During Long-Term Treatment with Tafamidis for Transthyretin Amyloidosis with Polyneuropathy: Clinical Trial Results up to 8.5 Years
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The impact of inotersen on Neuropathy Impairment Score in patients with hereditary transthyretin amyloidosis with polyneuropathy
Switching from inotersen to eplontersen in patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: analysis from NEURO-TTRansform
A Review of Patisiran (ONPATTRO®) for the Treatment of Polyneuropathy in People with Hereditary Transthyretin Amyloidosis
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Muscle quantitative MRI as a novel biomarker in hereditary transthyretin amyloidosis with polyneuropathy: a cross-sectional study
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