3D SURVEY TECHNIQUES FOR THE ARCHITECTUTAL RESTORATION: THE CASE OF ST. AGATA IN PISA von Bevilacqua, M. G., Caroti, G., Piemonte, A., Ruschi, P., Tenchini, L.

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Inherited defects of coagulation factor V: the hemorrhagic side von ASSELTA, R., TENCHINI, M. L., DUGA, S.

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Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene von Combi, Romina, Dalprà, Leda, Ferini-Strambi, Luigi, Tenchini, Maria L.

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The molecular basis of quantitative fibrinogen disorders von ASSELTA, R., DUGA, S., TENCHINI, M. L.

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Autosomal dominant nocturnal frontal lobe epilepsy: A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome von OLDANI, A, ZUCCONI, M, ASSELTA, R, MODUGNO, M, BONATI, M. T, DALPRA, L, MALCOVATI, M, TENCHINI, M. L, SMIRNE, S, FERINI-STRAMBI, L

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Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion von Duga, Stefano, Asselta, Rosanna, Santagostino, Elena, Zeinali, Sirous, Simonic, Tatjana, Malcovati, Massimo, Mannucci, Pier Mannuccio, Tenchini, Maria Luisa

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The DNA‐pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemia von MONALDINI, L., ASSELTA, R., MALCOVATI, M., TENCHINI, M. L., DUGA, S.

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Autosomal dominant nocturnal frontal lobe epilepsy. A critical overview von COMBI, Romina, DALPRA, Leda, TENCHINI, Maria Luisa, FERINI-STRAMBI, Luigi

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Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease von Ardizzone, S., Maconi, G., Bianchi, V., Russo, A., Colombo, E., Cassinotti, A., Penati, C., Tenchini, M.L., Bianchi Porro, G.

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Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain von Asselta, R., Montefusco, M. C., Duga, S., Malcovati, M., Peyvandi, F., Mannucci, P. M., Tenchini, M. L.

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The discovery of Mary's mutation von Asselta, R., Tenchini, M. L., Holme, R., Brosstad, F., Stormorken, H.

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A novel Chlamydomonas reinhardtii gene potentially encoding a proline-, glycine-, and tyrosine-rich protein (PGYRP) von Sangiorgio, Lorenzo, Strumbo, Bice, Tenchini, Maria L., Malcovati, Massimo, Ronchi, Severino, Simonic, Tatjana

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cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex von Simonic, T, Duga, S, Negri, A, Tedeschi, G, Malcovati, M, Tenchini, M L, Ronchi, S

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SER252PHE and 776INS3 mutations in the CHRNA4 gene are rare in the Italian ADNFLE population von TENCHINI, M. L, DUGA, S, BONATI, M. T, ASSELTA, R, OLDANI, A, ZUCCONI, M, MALCOVATI, M, DALPRA, L, FERINI-STRAMBI, L

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Coexistence of a novel homozygous nonsense mutation in exon 13 of the factor V gene with the homozygous Leiden mutation in two unrelated patients with severe factor V deficiency von Van Wijk, Richard, Montefusco, Maria Claudia, Duga, Stefano, Asselta, Rosanna, Van Solinge, Wouter, Malcovati, Massimo, Tenchini, Maria Luisa, Mannucci, Pier Mannuccio

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novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency von Bozzao, Cristina, Rimoldi, Valeria, Asselta, Rosanna, Landau, Meytal, Ghiotto, Rossella, Tenchini, Maria L, De Cristofaro, Raimondo, Castaman, Giancarlo, Duga, Stefano

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Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs von Asselta, Rosanna, Duga, Stefano, Spena, Silvia, Santagostino, Elena, Peyvandi, Flora, Piseddu, Gavino, Targhetta, Roberto, Malcovati, Massimo, Mannucci, Pier Mannuccio, Tenchini, Maria Luisa

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Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms von Duga, S., Soldà, G., Asselta, R., Bonati, M. T., Dalprà, L., Malcovati, M., Tenchini, M. L.

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Refined mapping of CHRNA3/A5/B4 gene cluster and its implications in ADNFLE von Bonati, Maria Teresa, Asselta, Rosanna, Duga, Stefano, Ferini-Strambi, Luigi, Oldani, Alessandro, Zucconi, Marco, Malcovati, Massimo, Dalprà, Leda, Tenchini, Maria Luisa

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Concerns about the Mutations Identified in a Case of Familial Coagulation Factor V Deficiency: Factor V Stanford von Montefusco, Maria Claudia, Asselta, Rosanna, van Wijk, Richard, Duga, Stefano, Tenchini, Maria Luisa

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