Lidia Larizza
Dipartimento di Medicina
Chirurgia e Odontoiatria
Università degli Studi di Milano
Milano
Italy
Name/email consistency: high
- Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations. Colombo, E.A., Bazan, J.F., Negri, G., Gervasini, C., Elcioglu, N.H., Yucelten, D., Altunay, I., Cetincelik, U., Teti, A., Del Fattore, A., Luciani, M., Sullivan, S.K., Yan, A.C., Volpi, L., Larizza, L. Orphanet. J. Rare. Dis (2012)
- Rothmund-Thomson syndrome. Larizza, L., Roversi, G., Volpi, L. Orphanet. J. Rare. Dis (2010)
- Developmental abnormalities and cancer predisposition in neurofibromatosis type 1. Larizza, L., Gervasini, C., Natacci, F., Riva, P. Curr. Mol. Med. (2009)
- Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping. Larizza, L., Magnani, I., Roversi, G. Cancer Lett. (2006)
- The Kasumi-1 cell line: a t(8;21)-kit mutant model for acute myeloid leukemia. Larizza, L., Magnani, I., Beghini, A. Leuk. Lymphoma (2005)
- Update on the cytogenetics and molecular genetics of chordoma. Larizza, L., Mortini, P., Riva, P. Hered. Cancer. Clin. Pract (2005)