• 2 Citations
  • 1 h-Index
20182019
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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.

  • 14 Similar Profiles
Myelin P0 Protein Medicine & Life Sciences
Myelin Proteins Medicine & Life Sciences
Nonsense Codon Medicine & Life Sciences
Myelin Sheath Medicine & Life Sciences
Integrins Medicine & Life Sciences
Paralysis Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Schwann Cells Medicine & Life Sciences

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Research Output 2018 2019

  • 2 Citations
  • 1 h-Index
  • 2 Article
2 Citations (Scopus)

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

Myelin P0 Protein
Nonsense Codon
Phenotype
Membranes
Myelin Sheath

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

Myelin Proteins
Integrins
Paralysis
Myelin Sheath
Pressure