AVEMARIA, FRANCESCA
AVEMARIA, FRANCESCA
Universita' degli Studi di MILANO
Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DM
2020 G. Sartore, E. Ragazzi, S. Burlina, R. Paleari, N.C. Chilelli, A. Mosca, F. Avemaria, A. Lapolla
DIABETES MELLITUS: A COMPLEX METABOLIC DISORDER.EXPLORING THE DISEASE THROUGH FRUCTOSAMINE 3-KINASE GENE ANALYSIS
2015 F. Avemaria
Possible role of fructosamine 3-kinase genotyping for the management of diabetic patients
2015 F. Avemaria, P. Carrera, A. Lapolla, G. Sartore, N.C. Chilelli, R. Paleari, A. Ambrosi, M. Ferrari, A. Mosca
PDCD10 gene mutations in multiple cerebral cavernous malformations
2014 M. Sole Cigoli, F. Avemaria, S. De Benedetti, G.P. Gesu, L. Giordano Accorsi, S. Parmigiani, M.F. Corona, V. Capra, A. Mosca, S. Giovannini, F. Notturno, F. Ciccocioppo, L. Volpi, M. Estienne, G. De Michele, A. Antenora, L. Bilo, A. Tavoni, N. Zamponi, E. Alfei, G. Baranello, D. Riva, S. Penco
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype
2014 C. Lunetta, V.A. Sansone, S. Penco, L. Mosca, C. Tarlarini, F. Avemaria, E. Maestri, M.G. Melazzini, G. Meola, M. Corbo
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations
2012 L. Mosca, S. Pileggi, F. Avemaria, C. Tarlarini, M.S. Cigoli, V. Capra, P. De Marco, M. Pavanello, A. Marocchi, S. Penco
Wide phenotypic spectrum of the TARDBP gene : homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject
2012 L. Mosca, C. Lunetta, C. Tarlarini, F. Avemaria, E. Maestri, M. Melazzini, M. Corbo, S. Penco
Phenotypic heterogeneity in a SOD1 G93D Italian ALS family : an example of human model to study a complex disease
2011 S. Penco, C. Lunetta, L. Mosca, E. Maestri, F. Avemaria, C. Tarlarini, M.C. Patrosso, A. Marocchi, M. Corbo
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression
2011 F. Avemaria, C. Lunetta, C. Tarlarini, L. Mosca, E. Maestri, A. Marocchi, M. Melazzini, S. Penco, M. Corbo