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Il Farmaco; Edizione Scientifica|July 1, 1984
[Synthesis and biological activity of new compounds with the 1,3-dioxol(4,5-g)quinoline structure]C Pellerano, L SaviniIl Farmaco; Edizione Scientifica|July 1, 1985
[Quinolylhydrazones with potential antimicrobial and antiparasitic activity]C Pellerano, L Savini, V BrizziBioorganic & Medicinal Chemistry|May 23, 1998
High affinity central benzodiazepine receptor ligands: synthesis and structure-activity relationship studies of a new series of pyrazolo[4,3-c]quinolin-3-onesL Savini, P Massarelli, C Nencini, et al.Farmaco (Societa Chimica Italiana : 1989)|February 7, 2002
Synthesis and pharmacological activity of 1,2,4-triazolo[4,3-a]quinolinesL Savini, L Chiasserini, C Pellerano, et al.Il Farmaco; Edizione Scientifica|December 1, 1975
Anticestode quinolinehydrazonesC Pellerano, L Savini, C E Berkoff, et al.Farmaco (Societa Chimica Italiana : 1989)|June 1, 1992
Quinolinehydrazones as inhibitors of retroviral reverse transcriptaseC Bartolucci, L Cellai, P Di Filippo, et al.Bioorganic & Medicinal Chemistry Letters|June 27, 2001
Novel and potent tacrine-related hetero- and homobivalent ligands for acetylcholinesterase and butyrylcholinesteraseL Savini, G Campiani, A Gaeta, et al.Bioorganic & Medicinal Chemistry|March 16, 2001
High affinity central benzodiazepine receptor ligands. Part 2: quantitative structure-activity relationships and comparative molecular field analysis of pyrazolo[4,3-c]quinolin-3-onesL Savini, L Chiasserini, C Pellerano, et al.Journal of Veterinary Medicine. B, Infectious Diseases and Veterinary Public Health|October 13, 2005
Comparison of BSE prevalence estimates from EU countries for the period July to December 2001 to the OIE and EU GBR classificationsA Giovannini, L Savini, A Conte, et al.Farmaco (Societa Chimica Italiana : 1989)|February 11, 2000
Synthesis, binding affinity and selectivity of new beta 1- and beta 2-adrenoceptor blockersV Brizzi, M Francioli, M Brufani, et al.Pageof 4