X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene von Villa, Anna, Notarangelo, Luigi, Macchi, Paolo, Mantuano, Elide, Cavagni, Giovanni, Brugnoni, Duilio, Strina, Dario, Patrosso, M Cristina, Ramenghi, Ugo, Grazia Sacco, Maria, Ugazio, Alberto, Vezzoni, Paolo

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Organization of the Human CD40L Gene: Implications for Molecular Defects in X Chromosome-Linked Hyper-IgM Syndrome and Prenatal Diagnosis von Villa, Anna, Notarangelo, Luigi D., Di Santo, James P., Macchi, Paolo P., Strina, Dario, Frattini, Annalisa, Lucchini, Franco, Patrosso, Cristina M., Giliani, Silvia, Mantuano, Elide, Agosti, Silvano, Nocera, Gianfranco, Kroczek, Richard A., Fischer, Alain, Ugazio, Alberto G., Genevieve de Saint Basile, Vezzoni, Paolo

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Fidelity of a YAC clone in the region of human MCF-2 gene von Cristina Patrosso, M., Frattini, Annalisa, Susani, Lucia, Vezzoni, Paolo, Villa, Anna

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Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis von Patrosso, M. Cristina, Salvi, Fabrizio, De Grandis, Domenico, Vezzoni, Paolo, Jacobson, Daniel R., Ferlini, Alessandra

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SOD1 mutations in amyotrophic lateral sclerosis : Results from a multicenter Italian study von BATTISTINI, Stefania, GIANNINI, Fabio, CAPONNETTO, Claudia, ORIGONE, Paola, MAROCCHI, Alessandro, DEL CORONA, Alberto, SICILIANO, Gabriele, CARRERA, Paola, MASCIA, Vincenzo, GIAGHEDDU, Marcello, CARCASSI, Carlo, ORRU, Sandro, GRECO, Giuseppe, GARRE, Cecilia, PENCO, Silvana, BIBBO, Giuseppe, FERRERA, Loretta, MARINI, Valeria, CAUSARANO, Renzo, CASULA, Michela, LANDO, Giuliana, PATROSSO, Maria Cristina

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Glutamate-cysteine ligase polymorphism, hypertension, and male sex are associated with cardiovascular events. Biochemical and genetic characterization of Italian subpopulation von Campolo, Jonica, MSc, Penco, Silvana, MSc, PhD, Bianchi, Elena, MSc, Colombo, Laura, MSc, Parolini, Marina, BStat, Caruso, Raffaele, MSc, Sedda, Valentina, MSc, Patrosso, Maria Cristina, MSc, Cighetti, Giuliana, ChD, Marocchi, Alessandro, MD, Parodi, Oberdan, MD

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Molecular Analysis of PDGFRA and PDGFRB Genes by Rapid Single-strand Conformation Polymorphism (SSCP) in Patients with Core-binding Factor Leukaemias with KIT or FLT3 Mutation von TROJANI, Alessandra, BARBARA RIPAMONTI, Carla, PEZZETTI, Laura, RAVELLI, Erica, PATROSSO, Maria Cristina, MAROCCHI, Alessandro, CUNEO, Antonio, FERRARA, Felicetto, LAZZARINO, Mario, PIZZOLO, Giovanni, CAIROLI, Roberto, MORRA, Enrica, PENCO, Silvana, BEGHINI, Alessandro, NADALI, Gianpaolo, DI BONA, Eros, VIOLA, Assunta, CASTAGNOLA, Carlo, COLAPIETRO, Patrizia, GRILLO, Giovanni

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An italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) von Ragno, Michele, Tournier-Lasserve, Elisabeth, Fiori, Mario G., Manca, Antonio, Patrosso, Maria Cristina, Ferlini, Alessandra, Sirocchi, Giovanna, Trojano, Luigi, Chabriat, Hugues, Salvi, Fabrizio

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5‐methyltetrahydrofolate restores endothelial function in uraemic patients on convective haemodialysis von Buccianti, Gherardo, Raselli, Sara, Baragetti, Ivano, Bamonti, Fabrizia, Corghi, Enzo, Novembrino, Cristina, Patrosso, Cristina, Maggi, Franco M., Catapano, Alberico L.

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Assay using succinyldithiocholine as substrate: The method of choice for the measurement of cholinesterase catalytic activity in serum to diagnose succinyldicholine sensitivity von MOSCA, Andrea, BONORA, Roberto, CERIOTTI, Ferruccio, FRANZINI, Carlo, LANDO, Giuliana, PATROSSO, Maria Cristina, ZANINOTTO, Martina, PANTEGHINI, Mauro

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Capillary electrophoresis of polymerase chain reaction-amplified products in polymer networks: The case of Kennedy's disease von Nesi, Marina, Righetti, Pier Giorgio, Patrosso, Maria Cristina, Ferlini, Alessandra, Chiari, Marcella

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A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis von Ferlini, Alessandra, Patrosso, Maria Cristina, Repetto, Monica, Frattini, Annalisa, Villa, Anna, Fini, Sergio, Salvi, Fabrizio, Vezzoni, Paolo, Forabosco, Antonino

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ZNF75: Isolation of a cDNA Clone of the KRAB Zinc Finger Gene Subfamily Mapped in YACs 1 Mb Telomeric of HPRT von Villa, Anna, Zucchi, Ileana, Pilia, Giuseppe, Strina, Dario, Susani, Lucia, Morali, Federica, Patrosso, Cristina, Frattini, Annalisa, Lucchini, Franco, Repetto, Monica, Sacco, Maria Grazia, Zoppè, Monica, Vezzoni, Paolo

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Methylation and sequence analysis around Eagi sites: identification of 28 new CpG islands in XQ24-XQ28 von Tribioli, Carla, Tamanini, Filippo, Patrosso, Cristina, Milanesi, Luciano, Villa, Anna, Pergolizzi, Rossana, Maestrini, Elena, Rivella, Stefano, Bione, Silvia, Mancini, Mita, Vezzoni, Paolo, Toniolo, Daniela

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Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to XQ28 Close to the L1CAM Gene von Frattini, A., Zucchi, I., Villa, A., Patrosso, C., Repetto, M., Susani, L., Strina, D., Redolfi, E., Vezzoni, P., Romano, G., Palmieri, G., Esposito, T., Durso, M.

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Decreased Affinity of Apolipoprotein AII to High-Density Lipoprotein in Patients with Transthyretin-Related Amyloidosis (Met30, Gln89, Pro36, and Thr34) von Nakamura, Masaaki, Tanaka, Yoshiya, Ando, Yukio, Yamashita, Taro, Salvi, Fabrizio, Ferlini, Alessandra, Gobbi, Paola, Patrosso, Cristina, Uchino, Makoto, Ando, Masayuki

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Isolation of a zinc finger motif (ZNF75) mapping on chromosome Xq26 von Villa, Anna, Patrosso, Cristina, Biunno, Ida, Frattini, Annalisa, Repetto, Monica, Mostardini, Marina, Evans, Glen, Susani, Lucia, Strina, Dario, Redolfi, Elena, Lazzari, Barbara, Pellegrini, Massimo, Vezzoni, Paolo

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Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study von LANDO, Giuliana, MOSCA, Andrea, BONORA, Roberto, AZZARIO, Franco, PENCO, Silvana, MAROCCHI, Alessandro, PANTEGHINI, Mauro, PATROSSO, Maria Cristina

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