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Nerve ultrasonography features in hereditary transthyretin amyloidosis with V30M mutation and polyneuropathy

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Data will be shared in anonymous form on a reasoned request to the corresponding author.

References

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Funding

The present study was supported by an Investigator-Initiated Research to University of Padova from Pfizer Inc. Pfizer Inc. had no role in the study design, data analysis, and results interpretation of the present study.

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Correspondence to Alessandro Salvalaggio.

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Competing interests

Alessandro Salvalaggio reports travel grants from Alnylam, Akcea and Pfizer and Speaker honoraria from Alnylam; Chiara Briani reports speaker and consulting honoraria from Akcea, Alnylam and Pfizer, and travel grants from Kedrion, Alnylam, and CSL Behring.

Ethics approval

The study was approved by the “Comitato Etico per la Sperimentazione Clinica della Provincia di Padova” and by local ethical committees of all the involved centres.

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Enrolled subjects gave written informed consent to participate to the study.

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Salvalaggio, A., Coraci, D., Cacciavillani, M. et al. Nerve ultrasonography features in hereditary transthyretin amyloidosis with V30M mutation and polyneuropathy. Neurol Sci 42, 2547–2548 (2021). https://doi.org/10.1007/s10072-020-05033-w

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  • DOI: https://doi.org/10.1007/s10072-020-05033-w

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