The control of allergic rhinitis in real life: a multicenter cross-sectional Italian study by Gani, Federica, Lombardi, Carlo, Barrocu, Laura, Landi, Massimo, Ridolo, Erminia, Bugiani, Massimo, Rolla, Giovanni, Senna, Gianenrico, Passalacqua, Giovanni

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Sex Differences in Severe Asthma: Results From Severe Asthma Network in Italy-SANI by Senna, Gianenrico, Latorre, Manuela, Bugiani, Massimo, Caminati, Marco, Heffler, Enrico, Morrone, Daniela, Paoletti, Giovanni, Parronchi, Paola, Puggioni, Francesca, Blasi, Francesco, Canonica, Giorgio Walter, Paggiaro, Pierluigi

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Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy by Fernandez-Vizarra, Erika, Bugiani, Marianna, Goffrini, Paola, Carrara, Franco, Farina, Laura, Procopio, Elena, Donati, Alice, Uziel, Graziella, Ferrero, Iliana, Zeviani, Massimo

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Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy by Malfatti, Edoardo, Bugiani, Marianna, Invernizzi, Federica, de Souza, Carolina Fischinger-Moura, Farina, Laura, Carrara, Franco, Lamantea, Eleonora, Antozzi, Carlo, Confalonieri, Paolo, Sanseverino, Maria Teresa, Giugliani, Roberto, Uziel, Graziella, Zeviani, Massimo

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Effects of riboflavin in children with complex II deficiency by Bugiani, Marianna, Lamantea, Eleonora, Invernizzi, Federica, Moroni, Isabella, Bizzi, Alberto, Zeviani, Massimo, Uziel, Graziella

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Frontotemporal Dementia and Corticobasal Degeneration in a Family with a P301S Mutation in Tau by Bugiani, Orso, Murrell, Jill R, Giaccone, Giorgio, Hasegawa, Masato, Ghigo, Giuseppe, Tabaton, Massimo, Morbin, Michela, Primavera, Alberto, Carella, Francesco, Solaro, Claudio, Grisoli, Marina, Savoiardo, Mario, Spillantini, Maria Grazia, Tagliavini, Fabrizio, Goedert, Michel, Ghetti, Bernardino

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MR Findings in Leigh Syndrome with COX Deficiency and SURF-1 Mutations by Farina, Laura, Chiapparini, Luisa, Uziel, Graziella, Bugiani, Marianna, Zeviani, Massimo, Savoiardo, Mario

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Phenotypic characterization of hypomyelination and congenital cataract by Biancheri, Roberta, Zara, Federico, Bruno, Claudio, Rossi, Andrea, Bordo, Laura, Gazzerro, Elisabetta, Sotgia, Federica, Pedemonte, Marina, Scapolan, Sara, Bado, Massimo, Uziel, Graziella, Bugiani, Marianna, Lamba, Laura Doria, Costa, Valeria, Schenone, Angelo, Rozemuller, Annemieke J. M., Tortori-Donati, Paolo, Lisanti, Michael P., van der Knaap, Marjo S., Minetti, Carlo

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Cohen syndrome resulting from a novel large intragenic COH1 deletion segregating in an isolated Greek island population by Bugiani, Marianna, Gyftodimou, Yolanda, Tsimpouka, Paraskevi, Lamantea, Eleonora, Katzaki, Eleni, d'Adamo, Pio, Nakou, Sheena, Georgoudi, Nelli, Grigoriadou, Maria, Tsina, Efthymia, Kabolis, Nikolaos, Milani, Donatella, Pandelia, Efthimia, Kokotas, Haris, Gasparini, Paolo, Giannoulia-Karantana, Aglaia, Renieri, Alessandra, Zeviani, Massimo, Petersen, Michael B.

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Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106–126 by Thellung, Stefano, Florio, Tullio, Corsaro, Alessandro, Arena, Sara, Merlino, Massimo, Salmona, Mario, Tagliavini, Fabrizio, Bugiani, Orso, Forloni, Gianluigi, Schettini, Gennaro

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