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Proceedings of the National Academy of Sciences of the United States of America|August 16, 2000
Computational evidence in favor of a two-state, two-mode model of the retinal chromophore photoisomerizationR González-Luque, M Garavelli, F Bernardi, et al.
The European Respiratory Journal|April 1, 1995
Swyer-James syndrome: bronchoalveolar lavage findings in two patientsF Bernardi, S Cazzato, V Poletti, et al.
Leukemia & Lymphoma|August 1, 1994
Combined surgery and chemotherapy in primary gastric non-Hodgkin's lymphoma: a retrospective study in sixty-six patientsL Rigacci, G Bellesi, R Alterini, et al.
Revista Da Sociedade Brasileira De Medicina Tropical|February 3, 1999
Influence of canine brain decomposition on laboratory diagnosis of rabiesA Albas, C I Ferrari, L H da Silva, et al.
Human Genetics|October 1, 1988
A frequent factor XII gene mutation in Hageman traitF Bernardi, G Marchetti, S Volinia, et al.
British Journal of Haematology|February 1, 1989
A recurrent missense mutation (Arg----Gln) and a partial deletion in factor VIII gene causing severe haemophilia AF Bernardi, S Volinia, P Patracchini, et al.
Neuroscience Letters|December 5, 1988
Evaluation of the toxicity of the dopaminergic neurotoxins MPTP and MPP+ in PC12 pheochromocytoma cells: binding and biological studiesM E Marongiu, M P Piccardi, F Bernardi, et al.
Blood|June 1, 1989
Partial gene deletion in a family with factor X deficiencyF Bernardi, G Marchetti, P Patracchini, et al.
European Heart Journal|June 19, 2002
Venous thromboembolism in young women; role of thrombophilic mutations and oral contraceptive useC Legnani, G Palareti, G Guazzaloca, et al.
Human Genetics|October 1, 1989
Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocationP Patracchini, E Calzolari, V Aiello, et al.
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