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Fingerprint Dive into the research topics where Francesca Cortini 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 45-year-old Italian male with p.(Gly1815Ser) FBN1 mutation causing a mild variant of Marfan syndrome: A case study

Cortini, F., Villa, C., Marinelli, B., Franchetti, S., Riboldi, L. & Bassotti, A., Apr 1 2020, In : Dermatologica Sinica. 38, 2, p. 98-101 4 p.

Research output: Contribution to journalArticle

  • Emerging roles of long non-coding RNAs in the pathogenesis of Alzheimer's disease

    Cortini, F., Roma, F. & Villa, C., Mar 1 2019, In : Ageing Research Reviews. 50, p. 19-26 8 p.

    Research output: Contribution to journalReview article

  • Understanding the basis of Ehlers–Danlos syndrome in the era of the next-generation sequencing

    Cortini, F., Villa, C., Marinelli, B., Combi, R., Pesatori, A. C. & Bassotti, A., May 6 2019, In : Archives of Dermatological Research. 311, 4, p. 265-275 11 p.

    Research output: Contribution to journalReview article

  • Ehlers-danlos syndrome caused by the c.934C>T, p. Arg312Cys mutation in COL1A1 gene: An Italian family without cardio-vascular events

    Cortini, F., Marinelli, B., Seia, M., Seresini, A. & Bassotti, A., Jul 1 2018, In : Dermatology Online Journal. 24, 7, 9.

    Research output: Contribution to journalArticle