1985 …2019

Research output per year

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

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Research Output

Clinical features and therapeutic challenges of cytopenias belonging to alps and alps-related (ARS) phenotype

Palmisani, E., Miano, M., Micalizzi, C., Calvillo, M., Pierri, F., Terranova, P., Lanza, T., Lanciotti, M., Riccardi, F., Todiere, A., Zanardi, S., Caviglia, I., Dufour, C. & Fioredda, F., Mar 2019, In : British Journal of Haematology. 184, 5, p. 861-864 4 p.

Research output: Contribution to journalArticle

FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 gene

Miano, M., Cappelli, E., Pezzulla, A., Venè, R., Grossi, A., Terranova, P., Palmisani, E., Maggiore, R., Guardo, D., Lanza, T., Calvillo, M., Micalizzi, C., Pierri, F., Vernarecci, C., Beccaria, A., Corsolini, F., Lanciotti, M., Russo, G., Ceccherini, I., Dufour, C. & 1 others, Fioredda, F., 2019, In : British Journal of Haematology. 187, 4, p. 502-508 7 p.

Research output: Contribution to journalArticle

  • FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 gene

    Miano, M., Cappelli, E., Pezzulla, A., Venè, R., Grossi, A., Terranova, P., Palmisani, E., Maggiore, R., Guardo, D., Lanza, T., Calvillo, M., Micalizzi, C., Pierri, F., Vernarecci, C., Beccaria, A., Corsolini, F., Lanciotti, M., Russo, G., Ceccherini, I., Dufour, C. & 1 others, Fioredda, F., 2019, In : British Journal of Haematology. 187, 4, p. 502-508 7 p.

    Research output: Contribution to journalArticle

    Long-term use of pegfilgrastim in children with severe congenital neutropenia: Clinical and pharmacokinetic data

    Fioredda, F., Lanza, T., Gallicola, F., Riccardi, F., Lanciotti, M., Mastrodicasa, E., Signa, S., Zanardi, S., Calvillo, M. & Dufour, C., Oct 27 2016, In : Blood. 128, 17, p. 2178-2181 4 p.

    Research output: Contribution to journalLetter

    AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia

    Virts, E. L., Jankowska, A., Mackay, C., Glaas, M. F., Wiek, C., Kelich, S. L., Lottmann, N., Kennedy, F. M., Marchal, C., Lehnert, E., Scharf, R. E., Dufour, C., Lanciotti, M., Farruggia, P., Santoro, A., Savasan, S., Scheckenbach, K., Schipper, J., Wagenmann, M., Lewis, T. & 12 others, Leffak, M., Farlow, J. L., Foroud, T. M., Honisch, E., Niederacher, D., Chakraborty, S. C., Vance, G. H., Pruss, D., Timms, K. M., Lanchbury, J. S., Alpi, A. F. & Hanenberg, H., Apr 9 2015, In : Human Molecular Genetics. 24, 18, p. 5093-5108 16 p., ddv227.

    Research output: Contribution to journalArticle