TARLARINI, CLAUDIA
TARLARINI, CLAUDIA
Dipartimento di Scienze Farmacologiche e Biomolecolari
Neurophysiological indices in amyotrophic lateral sclerosis correlate with functional outcome measures, staging and disease progression
2021 A. Barp, A. Lizio, F. Gerardi, C. Tarlarini, M. Luca, V. Sansone, C. Lunetta
Urinary neopterin, a new marker of the neuroinflammatory status in amyotrophic lateral sclerosis
2020 C. Lunetta, A. Lizio, F. Gerardi, C. Tarlarini, M. Filippi, N. Riva, L. Tremolizzo, S. Diamanti, C. Dellanoce, L. Mosca, V. Sansone, J. Campolo
Taste changes in amyotrophic lateral sclerosis and effects on quality of life
2019 C. Tarlarini, L. Greco, A. Lizio, F. Gerardi, V. Sansone, C. Lunetta
MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS
2014 C. Tarlarini
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