1991 …2020

Research output per year

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

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Research Output

Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype

Khan, A. W., Minelli, A., Frattini, A., Montalbano, G., Bogni, A., Fabbri, M., Porta, G., Acquati, F., Pinto, R. M., Bergami, E., Mura, R., Pegoraro, A., Cesaro, S., Cipolli, M., Zecca, M., Danesino, C., Locatelli, F., Maserati, E., Pasquali, F. & Valli, R., Jan 2 2020, In : Molecular Cytogenetics. 13, 1, 1.

Research output: Contribution to journalArticle

Open Access
  • Validation of the Italian version of carers’ quality-of-life questionnaire for parkinsonism (PQoL Carer) in progressive supranuclear palsy

    Picillo, M., Cuoco, S., Amboni, M., Bonifacio, F. P., Bruno, A., Bruschi, F., Cappiello, A., De Micco, R., De Rosa, A., Di Biasio, F., Elifani, F., Erro, R., Fabbri, M., Falla, M., Franco, G., Frosini, D., Galantucci, S., Lazzeri, G., Magistrelli, L., Malaguti, M. C. & 23 others, Milner, A. V., Minafra, B., Olivola, E., Pilotto, A., Rascunà, C., Rizzetti, M. C., Schirinzi, T., Borroni, B., Ceravolo, R., Di Fonzo, A., Lopiano, L., Marchese, R., Mercuri, N. B., Modugno, N., Nicoletti, A., Padovani, A., Santangelo, G., Stefani, A., Tessitore, A., Volontè, M. A., Zangaglia, R., Zappia, M. & Barone, P., 2019, In : Neurological Sciences. 40, 10, p. 2163-2169

    Research output: Contribution to journalArticle

    Validation of the Italian version of the PSP Quality of Life questionnaire: Neurological Sciences

    Picillo, M., Cuoco, S., Amboni, M., Bonifacio, F. P., Bruschi, F., Carotenuto, I., De Micco, R., De Rosa, A., Del Prete, E., Di Biasio, F., Elifani, F., Erro, R., Fabbri, M., Falla, M., Franco, G., Frosini, D., Galantucci, S., Lazzeri, G., Magistrelli, L., Malaguti, M. C. & 23 others, Milner, A. V., Minafra, B., Olivola, E., Pilotto, A., Rascunà, C., Rizzetti, M. C., Schirinzi, T., Borroni, B., Ceravolo, R., Di Fonzo, A., Marchese, R., Mercuri, N. B., Modugno, N., Nicoletti, A., Padovani, A., Santangelo, G., Stefani, A., Tessitore, A., Volontè, M. A., Zangaglia, R., Zappia, M., Zibetti, M. & Barone, P., 2019, In : Neurol. Sci.. 40, 12, p. 2587-2594

    Research output: Contribution to journalArticle

    Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene

    Valli, R., Vinti, L., Frattini, A., Fabbri, M., Montalbano, G., Olivieri, C., Minelli, A., Locatelli, F., Pasquali, F. & Maserati, E., Jan 11 2018, In : Molecular Cytogenetics. 11, 1, 2.

    Research output: Contribution to journalArticle

  • Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene

    Valli, R., Vinti, L., Frattini, A., Fabbri, M., Montalbano, G., Olivieri, C., Minelli, A., Locatelli, F., Pasquali, F. & Maserati, E., 2018, In : Molecular Cytogenetics. 11, p. 2 9 p.

    Research output: Contribution to journalArticle