20182019

Research output per year

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Fingerprint Dive into the research topics where Desiree Zambroni 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 nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function: Human molecular genetics

Fratta, P., Ornaghi, F., Dati, G., Zambroni, D., Saveri, P., Belin, S., D'Adamo, P., Shy, M., Quattrini, A., Feltri, ML. & Wrabetz, L., 2019, In : Human Molecular Genetics. 28, 1, p. 124-132 9 p.

Research output: Contribution to journalArticle

  • A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function

    Fratta, P., Ornaghi, F., Dati, G., Zambroni, D., Saveri, P., Belin, S., D'Adamo, P., Shy, M., Quattrini, A., Laura Feltri, M. & Wrabetz, L., Jan 1 2019, In : Human Molecular Genetics. 28, 1, p. 124-132 9 p.

    Research output: Contribution to journalArticle

  • Enhanced axonal neuregulin-1 type-III signaling ameliorates neurophysiology and hypomyelination in a Charcot-Marie-Tooth type 1B mouse model

    Scapin, C., Ferri, C., Pettinato, E., Zambroni, D., Bianchi, F., Carro, U. D., Belin, S., Caruso, D., Mitro, N., Pellegatta, M., Taveggia, C., Schwab, M. H., Nave, K. A., Laura Feltri, M., Wrabetz, L. & D'Antonio, M., Mar 2019, In : Human Molecular Genetics. 28, 6, p. 992-1006 15 p.

    Research output: Contribution to journalArticle

  • A dual role for Integrin α6β4 in modulating hereditary neuropathy with liability to pressure palsies

    Poitelon, Y., Matafora, V., Silvestri, N., Zambroni, D., McGarry, C., Serghany, N., Rush, T., Vizzuso, D., Court, FA., Bachi, A., Wrabetz, L. & Feltri, ML., 2018, In : Journal of Neurochemistry. 145, 3, p. 245-257 13 p.

    Research output: Contribution to journalArticle