A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield von Ankala, Arunkanth, da Silva, Cristina, Gualandi, Francesca, Ferlini, Alessandra, Bean, Lora J. H., Collins, Christin, Tanner, Alice K., Hegde, Madhuri R.

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Human mesenchymal stem cells modulate B-cell functions von Corcione, Anna, Benvenuto, Federica, Ferretti, Elisa, Giunti, Debora, Cappiello, Valentina, Cazzanti, Francesco, Risso, Marco, Gualandi, Francesca, Mancardi, Giovanni Luigi, Pistoia, Vito, Uccelli, Antonio

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New Clinical and Immunofluorescence Data of Collagen VI-Related Myopathy: A Single Center Cohort of 69 Patients von Merlini, Luciano, Sabatelli, Patrizia, Gualandi, Francesca, Redivo, Edoardo, Di Martino, Alberto, Faldini, Cesare

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Attention Deficit Hyperactivity Disorder and Cognitive Function in Duchenne Muscular Dystrophy: Phenotype-Genotype Correlation von Pane, Marika, MD, Lombardo, Maria Elena, MD, Alfieri, Paolo, MD, D'Amico, Adele, MD, Bianco, Flaviana, MD, Vasco, Gessica, MD, Piccini, Giorgia, Dpsych, Mallardi, Maria, Dpsych, Romeo, Domenico M., MD, Ricotti, Valeria, MD, Ferlini, Alessandra, MD, Gualandi, Francesca, MD, Vicari, Stefano, MD, Bertini, Enrico, MD, Berardinelli, Angela, MD, Mercuri, Eugenio, MD

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The medical genetics of dystrophinopathies: Molecular genetic diagnosis and its impact on clinical practice von Ferlini, Alessandra, Neri, Marcella, Gualandi, Francesca

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Second haploidentical stem cell transplantation for primary graft failure von Giammarco, Sabrina, Raiola, Anna Maria, Di Grazia, Carmen, Bregante, Stefania, Gualandi, Francesca, Varaldo, Riccardo, Chiusolo, Patrizia, Sora, Federica, Sica, Simona, Laurenti, Luca, Metafuni, Elisabetta, Innocenti, Idanna, Autore, Francesco, Murgia, Barbara, Bacigalupo, Andrea, Angelucci, Emanuele

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Direct intrabone transplant of unrelated cord-blood cells in acute leukaemia: a phase I/II study von Frassoni, Francesco, Dr, Gualandi, Francesca, MD, Podestà, Marina, PhD, Raiola, Anna Maria, MD, Ibatici, Adalberto, MD, Piaggio, Giovanna, PhD, Sessarego, Mario, Prof, Sessarego, Nadia, PhD, Gobbi, Marco, Prof, Sacchi, Nicoletta, PhD, Labopin, Myriam, MD, Bacigalupo, Andrea, MD

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Treatment of steroid resistant acute graft versus host disease with an anti-CD26 monoclonal antibody—Begelomab von Bacigalupo, Andrea, Angelucci, Emanuele, Raiola, Anna Maria, Varaldo, Riccardo, Di Grazia, Carmen, Gualandi, Francesca, Benedetti, Edoardo, Risitano, Antonio, Musso, Maurizio, Zallio, Francesco, Ciceri, Fabio, Chiusolo, Patrizia, Sica, Simona, Rambaldi, Alessandro, Bonifazi, Francesca, Parma, Matteo, Martino, Massimo, Onida, Francesco, Iori, Anna Paola, Selleri, Carmine, Borghero, Carlo, Bertaina, Alice, Prezioso, Lucia, Algeri, Mattia, Locatelli, Franco

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Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes von Zanotti, Simona, Magri, Francesca, Salani, Sabrina, Napoli, Laura, Ripolone, Michela, Ronchi, Dario, Fortunato, Francesco, Ciscato, Patrizia, Velardo, Daniele, D'Angelo, Maria Grazia, Gualandi, Francesca, Nigro, Vincenzo, Sciacco, Monica, Corti, Stefania, Comi, Giacomo Pietro, Piga, Daniela

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Charcot-Marie-Tooth Disease with Myelin Protein Zero Mutation Presenting as Painful, Predominant Small-Fiber Neuropathy von Gemignani, Franco, Percesepe, Antonio, Gualandi, Francesca, Allegri, Isabella, Bellanova, Maria Federica, Nuredini, Andi, Saccani, Elena, Ambrosini, Enrico, Barili, Valeria, Uliana, Vera

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Genetic testing offer for inherited neuromuscular diseases within the EURO-NMD reference network: A European survey study von Peterlin, Borut, Gualandi, Francesca, Maver, Ales, Servidei, Serenella, van der Maarel, Silvère M, Lamy, Francoise, Mejat, Alexander, Evangelista, Teresinha, Ferlini, Alessandra

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Natural history of pulmonary function in collagen VI-related myopathies von FOLEY, A. Reghan, QUIJANO-ROY, Susana, NORTH, Kathryn, RYAN, Monique M, RICHARD, Pascale, ALLAMAND, Valérie, HICKS, Debbie, LAMANDE, Shireen, YING HU, GUALANDI, Francesca, SUNGYOUNG AUH, MUNTONI, Francesco, COLLINS, James, BÖNNEMANN, Carsten G, STRAUB, Volker, MCCALLUM, Michelle, DECONINCK, Nicolas, MERCURI, Eugenio, PANE, Marika, D'AMICO, Adele, BERTINI, Enrico

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Steroid treatment of acute graft- versus -host disease grade I: a randomized trial von Bacigalupo, Andrea, Milone, Giuseppe, Cupri, Alessandra, Severino, Antonio, Fagioli, Franca, Berger, Massimo, Santarone, Stella, Chiusolo, Patrizia, Sica, Simona, Mammoliti, Sonia, Sorasio, Roberto, Massi, Daniela, Van Lint, Maria Teresa, Raiola, Anna Maria, Gualandi, Francesca, Selleri, Carmine, Sormani, Maria Pia, Signori, Alessio, Risitano, Antonio, Bonifazi, Francesca

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Congenital Muscular Dystrophies: A Brief Review von Bertini, Enrico, MD, D'Amico, Adele, MD, PhD, Gualandi, Francesca, PhD, Petrini, Stefania, PhD

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Secondary autoimmune diseases occurring after HSCT for an autoimmune disease: a retrospective study of the EBMT Autoimmune Disease Working Party von Daikeler, Thomas, Labopin, Myriam, Di Gioia, Massimo, Abinun, Mario, Alexander, Tobias, Miniati, Irene, Gualandi, Francesca, Fassas, Athanasios, Martin, Thierry, Schwarze, Carl Philipp, Wulffraat, Nico, Buch, Maya, Sampol, Antonia, Carreras, Enric, Dubois, Benedicte, Gruhn, Bernd, Güngör, Tayfun, Pohlreich, David, Schuerwegh, Annemie, Snarski, Emilian, Snowden, John, Veys, Paul, Fasth, Anders, Lenhoff, Stig, Messina, Chiara, Voswinkel, Jan, Badoglio, Manuela, Henes, Jörg, Launay, David, Tyndall, Alan, Gluckman, Eliane, Farge, Dominique

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Affinity proteomics within rare diseases: a BIO‐NMD study for blood biomarkers of muscular dystrophies von Ayoglu, Burcu, Chaouch, Amina, Lochmüller, Hanns, Politano, Luisa, Bertini, Enrico, Spitali, Pietro, Hiller, Monika, Niks, Eric H, Gualandi, Francesca, Pontén, Fredrik, Bushby, Kate, Aartsma‐Rus, Annemieke, Schwartz, Elena, Le Priol, Yannick, Straub, Volker, Uhlén, Mathias, Cirak, Sebahattin, ‘t Hoen, Peter A C, Muntoni, Francesco, Ferlini, Alessandra, Schwenk, Jochen M, Nilsson, Peter, Al‐Khalili Szigyarto, Cristina

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Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of... von Puyade, Mathieu, Patel, Amit, Lim, Yeong Jer, Blank, Norbert, Badoglio, Manuela, Gualandi, Francesca, Ma, David D., Maximova, Natalia, Greco, Raffaella, Alexander, Tobias, Snowden, John A.

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Report of a novel ATP7A mutation causing distal motor neuropathy von Gualandi, Francesca, Sette, Elisabetta, Fortunato, Fernanda, Bigoni, Stefania, De Grandis, Domenico, Scotton, Chiara, Selvatici, Rita, Neri, Marcella, Incensi, Alex, Liguori, Rocco, Storbeck, Markus, Karakaya, Mert, Simioni, Valentina, Squarzoni, Stefano, Timmerman, Vincent, Wirth, Brunhilde, Donadio, Vincenzo, Tugnoli, Valeria, Ferlini, Alessandra

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Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins von Angelin, Alessia, Tiepolo, Tania, Sabatelli, Patrizia, Grumati, Paolo, Bergamin, Natascha, Golfieri, Cristina, Mattioli, Elisabetta, Gualandi, Francesca, Ferlini, Alessandra, Merlini, Luciano, Maraldi, Nadir M, Bonaldo, Paolo, Bernardi, Paolo

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Functional Characterization of Two Novel Mutations in SCN5A Associated with Brugada Syndrome Identified in Italian Patients von Balla, Cristina, Conte, Elena, Selvatici, Rita, Marsano, Renè Massimiliano, Gerbino, Andrea, Farnè, Marianna, Blunck, Rikard, Vitali, Francesco, Armaroli, Annarita, Brieda, Alessandro, Liantonio, Antonella, De Luca, Annamaria, Ferlini, Alessandra, Rapezzi, Claudio, Bertini, Matteo, Gualandi, Francesca, Imbrici, Paola

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