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Fingerprint Dive into the research topics where Emilia Bellone is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis?

Gotta, F., Lamp, M., Geroldi, A., Trevisan, L., Origone, P., Fugazza, G., Fabbri, S., Nesti, C., Rubegni, A., Morani, F., Santorelli, F. M., Bellone, E. & Mandich, P., Jan 1 2020, (Accepted/In press) In : Annals of Human Genetics.

Research output: Contribution to journalArticle

  • Diagnostic Value of Sural Nerve Biopsy: Retrospective Analysis of Clinical Cases From 1981 to 2017

    Prada, V., Massucco, S., Venturi, C., Geroldi, A., Bellone, E., Mandich, P., Minuto, M., Varaldo, E., Mancardi, G., Grandis, M. & Schenone, A., Nov 22 2019, In : Frontiers in Neurology. 10, 1218.

    Research output: Contribution to journalArticle

    Open Access
  • Expanding the spectrum of genes responsible for hereditary motor neuropathies

    Previtali, S. C., Zhao, E., Lazarevic, D., Pipitone, G. B., Fabrizi, G. M., Manganelli, F., Mazzeo, A., Pareyson, D., Schenone, A., Taroni, F., Vita, G., Bellone, E., Ferrarini, M., Garibaldi, M., Magri, S., Padua, L., Pennisi, E., Pisciotta, C., Riva, N., Scaioli, V. & 11 others, Scarlato, M., Tozza, S., Geroldi, A., Jordanova, A., Ferrari, M., Molineris, I., Reilly, M. M., Comi, G., Carrera, P., Devoto, M. & Bolino, A., Oct 1 2019, In : Journal of Neurology, Neurosurgery and Psychiatry. 90, 10, p. 1171-1179 9 p.

    Research output: Contribution to journalArticle

  • Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients

    Origone, P., Geroldi, A., Lamp, M., Sanguineri, F., Caponnetto, C., Cabona, C., Gotta, F., Trevisan, L., Bellone, E., Manganelli, F., Devigili, G. & Mandich, P., Mar 20 2019, In : Neurodegenerative Diseases.

    Research output: Contribution to journalArticle

  • Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise"

    Grandis, M., Geroldi, A., Gulli, R., Manganelli, F., Gotta, F., Lamp, M., Origone, P., Trevisan, L., Gemelli, C., Fabbri, S., Schenone, A., Tozza, S., Santoro, L., Bellone, E. & Mandich, P., Oct 4 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 177.

    Research output: Contribution to journalArticle