Volatolomics of Sardinian and Spanish Bituminaria : Characterization of Different Accessions Using Chemometrics von Usai, Marianna, Marchetti, Mauro, Melis, Rita A M, Porqueddu, Claudio

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The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011) von Pelo, E., Radice, P., Ravani, A., Resta, N., Russo, S., Seia, M., Varesco, L., Falbo, V., Taruscio, D., Melis, M. A., Grasso, M., Baffico, A. M., Salvatore, M., Marra, M., Floridia, G., Tosto, F., Censi, F., Rosatelli, C.

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The role of institutional investors in enacting stewardship by corporate boards von Melis, Danielle A.M, Nijhof, André

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Hyperbilirubinaemia in heterozygous β‐thalassaemia is related to co‐inherited Gilbert's syndrome von Galanello, R., Perseu, L., Melis, M. A., Cipollina, L., Barella, S., Giagu, N., Turco, M. P., Maccioni, O., Cao, A.

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Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy von Muntoni, Francesco, Di Lenarda, Andrea, Porcu, Maurizio, Sinagra, Gianfranco, Mateddu, Anna, Marrosu, Gianni, Ferlini, Alessandra, Cau, Milena, Milasin, Jelena, Melis, Maria Antonietta, Marrosu, Maria Giovanna, Cianchetti, Carlo, Sanna, Antonio, Falaschi, Arturo, Camerini, Fulvio, Giacca, Mauro, Mestroni, Luisa

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Bio‐agronomic characterization and implications on the potential use as forage of Bituminaria bituminosa and B. morisiana accessions von Melis, R. A. M., Franca, A., Re, G. A., Porqueddu, C.

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Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy von MUNTONI, F, MELIS, M. A, GANAU, A, DUBOWITZ, V

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Pregnancy decision-making in women with multiple sclerosis treated with natalizumab: I: Fetal risks von Portaccio, Emilio, Annovazzi, Pietro, Ghezzi, Angelo, Zaffaroni, Mauro, Moiola, Lucia, Martinelli, Vittorio, Lanzillo, Roberta, Brescia Morra, Vincenzo, Rinaldi, Francesca, Gallo, Paolo, Tortorella, Carla, Paolicelli, Damiano, Pozzilli, Carlo, De Giglio, Laura, Cavalla, Paola, Cocco, Eleonora, Marrosu, Maria Giovanna, Patti, Francesco, Solaro, Claudio, Bellantonio, Paolo, Uccelli, Antonio, Laroni, Alice, Pastò, Luisa, Giannini, Marta, Trojano, Maria, Comi, Giancarlo, Amato, Maria Pia

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Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism von Quadri, Marialuisa, Fang, Mingyan, Picillo, Marina, Olgiati, Simone, Breedveld, Guido J., Graafland, Josja, Wu, Bin, Xu, Fengping, Erro, Roberto, Amboni, Marianna, Pappatà, Sabina, Quarantelli, Mario, Annesi, Grazia, Quattrone, Aldo, Chien, Hsin F., Barbosa, Egberto R., Oostra, Ben A., Barone, Paolo, Wang, Jun, Bonifati, Vincenzo

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Pregnancy decision-making in women with multiple sclerosis treated with natalizumab: II: Maternal risks von Portaccio, Emilio, Moiola, Lucia, Martinelli, Vittorio, Annovazzi, Pietro, Ghezzi, Angelo, Zaffaroni, Mauro, Lanzillo, Roberta, Brescia Morra, Vincenzo, Rinaldi, Francesca, Gallo, Paolo, Tortorella, Carla, Paolicelli, Damiano, Pozzilli, Carlo, De Giglio, Laura, Cavalla, Paola, Cocco, Eleonora, Marrosu, Maria Giovanna, Solaro, Claudio, Uccelli, Antonio, Laroni, Alice, Pastò, Luisa, Giannini, Marta, Trojano, Maria, Comi, Giancarlo, Amato, Maria Pia

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Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families von Melis, MA, Cau, M, Muntoni, F, Mateddu, A, Galanello, R, Boccone, L, Deidda, F, Loi, D, Cao, A

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Does good corporate governance lead to better firm performance? Strategic lessons from a structured literature review von Khan, Bushra, Nijhof, André, Diepeveen, Rosalien A., Melis, Daniëlle A. M.

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A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron von Melis, Maria Antonietta, Cau, Milena, Congiu, Rita, Sole, Gabriella, Barella, Susanna, Cao, Antonio, Westerman, Mark, Cazzola, Mario, Galanello, Renzo

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Heterozygous β‐thalassemia with thalassemia intermedia phenotype von Gasperini, D., Perseu, L., Melis, M.A., Maccioni, L., Sollaino, M.C., Paglietti, E., Cao, A., Galanello, R.

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PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology von Wong, Tsz Hang, Chiu, Wang Zheng, Breedveld, Guido J., Li, Ka Wan, Verkerk, Annemieke J. M. H., Hondius, David, Hukema, Renate K., Seelaar, Harro, Frick, Petra, Severijnen, Lies-Anne, Lammers, Gert-Jan, Lebbink, Joyce H. G., van Duinen, Sjoerd G., Kamphorst, Wouter, Rozemuller, Annemieke J., Bakker, E. Bert, Neumann, Manuela, Willemsen, Rob, Bonifati, Vincenzo, Smit, August B., van Swieten, John

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Brief report : deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy von MUNTONI, F, CAU, M, MELIS, M. A, GANAU, A, CONGIU, R, ARVEDI, G, MATEDDU, A, MARROSU, M. G, CIANCHETTI, C, REALDI, G, CAO, A

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Optimal efficacy of interferon-free HCV retreatment after protease inhibitor failure in real life von Cento, V., Barbaliscia, S., Lenci, I., Ruggiero, T., Magni, C.F., Paolucci, S., Babudieri, S., Siciliano, M., Pasquazzi, C., Ciancio, A., Perno, C.F., Ceccherini-Silberstein, F., Micheli, V., Troshina, Y., Biliotti, E., Milana, M., Melis, M., Teti, E., Lambiase, L., Menzaghi, B., Nicolini, L.A., Marenco, S., Di Maio, V.C., Aragri, M., Pecchioli, A., Bertoli, A., Sarrecchia, C., Macera, M., Coppola, N., Puoti, M., Romagnoli, D., Pellicelli, A., Bonora, S., Novati, S., Baldanti, F., Ghisetti, V., Andreoni, M., Taliani, G., Rizzardini, G., Angelico, M.

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Hemoglobin Cagliari (β 60 [E4] VAL → GLU): A Novel Unstable Thalassemic Hemoglobinopathy von Podda, A., Galanello, R., Maccioni, L., Melis, M.A., Rosatelli, C., Perseu, L., Cao, A.

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X-linked dilated cardiomyopathy and the dystrophin gene von Ferlini, Alessandra, Sewry, Caroline, Melis, Maria Antonietta, Mateddu, Anna, Muntoni, Francesco

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Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy von Muntoni, F, Mateddu, A, Cianchetti, C, Marrosu, M G, Clerk, A, Cau, M, Congiu, R, Cao, A, Melis, M A

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