Dominant inheritance of a novel integrin β3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families von GRESELE, Paolo, FALCINELLI, Emanuela, NORIS, Patrizia, BAIDUINI, Carlo L, SAVOIA, Anna, GIANNINI, Silvia, D'ADAMO, Pio, D'EUSTACCHIO, Angela, CORAZZI, Teresa, MEZZASOMA, Anna Maria, DI BARI, Filomena, GUGLIELMINI, Giuseppe, CECCHETTI, Luca

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Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations von Savoia, Anna, Dufour, Carlo, Locatelli, Franco, Noris, Patrizia, Ambaglio, Chiara, Rosti, Vittorio, Zecca, Marco, Ferrari, Simona, di Bari, Filomena, Corcione, Anna, Di Stazio, Mariateresa, Seri, Marco, Balduini, Carlo L

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Cleft lip with or without cleft palate: implication of the heavy chain of non-muscle myosin IIA von Martinelli, Marcella, Di Stazio, Mariateresa, Scapoli, Luca, Marchesini, Jlenia, Di Bari, Filomena, Pezzetti, Furio, Carinci, Francesco, Palmieri, Annalisa, Carinci, Paolo, Savoia, Anna

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Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history ofMYH9-related disease von Pecci, Alessandro, Panza, Emanuele, Pujol-Moix, Núria, Klersy, Catherine, Di Bari, Filomena, Bozzi, Valeria, Gresele, Paolo, Lethagen, Stefan, Fabris, Fabrizio, Dufour, Carlo, Granata, Antonio, Doubek, Michael, Pecoraro, Carmine, Koivisto, Pasi A., Heller, Paula G., Iolascon, Achille, Alvisi, Patrizia, Schwabe, Dirk, De Candia, Erica, Rocca, Bianca, Russo, Umberto, Ramenghi, Ugo, Noris, Patrizia, Seri, Marco, Balduini, Carlo L., Savoia, Anna

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Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease von Pecci, Alessandro, Panza, Emanuele, Pujol-Moix, Núria, Klersy, Catherine, Di Bari, Filomena, Bozzi, Valeria, Gresele, Paolo, Lethagen, Stefan, Fabris, Fabrizio, Dufour, Carlo, Granata, Antonio, Doubek, Michael, Pecoraro, Carmine, Koivisto, Pasi A, Heller, Paula G, Iolascon, Achille, Alvisi, Patrizia, Schwabe, Dirk, De Candia, Erica, Rocca, Bianca, Russo, Umberto, Ramenghi, Ugo, Noris, Patrizia, Seri, Marco, Balduini, Carlo L, Savoia, Anna

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Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients von Noris, P, Pecci, A, Di Bari, F, Di Stazio, MT, Di Pumpo, M, Ceresa, IF, Arezzi, N, Ambaglio, C, Savoia, A, Balduini, CL

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Dominant inheritance of a novel integrin {beta}3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families von Gresele, Paolo, Falcinelli, Emanuela, Giannini, Silvia, D'Adamo, Pio, D'Eustacchio, Angela, Corazzi, Teresa, Mezzasoma, Anna Maria, Di Bari, Filomena, Guglielmini, Giuseppe, Cecchetti, Luca, Noris, Patrizia, Balduini, Carlo L, Savoia, Anna

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Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene von SERI, Marco, SAVINO, Maria, LANDOLFI, Raffaele, BALDUINI, Carlo L, ZELANTE, Leopoldo, RAVAZZOLO, Roberto, RENIERI, Alessandra, SAVOIA, Anna, BORDO, Domenico, CUSANO, Roberto, ROCCA, Bianca, MELONI, Ilaria, DI BARI, Filomena, KOIVISTO, Pasi A, BOLOGNESI, Martino, GHIGGERI, Gian Marco

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OR-41: Gadolinium-enhanced magnetic resonance (Gd-MR) as first approach in the diagnosis of renal artery stenosis von Rubbiani, Elisabetta, Giovannone, Carmela, Di Bari, Filomena, Inguaggiato, Paola, Albertazzi, Alberto, Colopi, Stefano, Cerofolini, Emilio, Marchetti, Mauro, Gallo, Ennio

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Dominant inheritance of a novel integrin beta3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families von Gresele, Paolo, Falcinelli, Emanuela, Giannini, Silvia, D'Adamo, Pio, D'Eustacchio, Angela, Corazzi, Teresa, Mezzasoma, Anna Maria, Di Bari, Filomena, Guglielmini, Giuseppe, Cecchetti, Luca, Noris, Patrizia, Balduini, Carlo L, Savoia, Anna

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Gadolinium-enhanced magnetic resonance (Gd-MR) as first approach in the diagnosis of renal artery stenosis von Rubbiani, Elisabetta, Giovannone, Carmela, Di Bari, Filomena, Inguaggiato, Paola, Albertazzi, Alberto, Colopi, Stefano, Cerofolini, Emilio, Marchetti, Mauro, Gallo, Ennio

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MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single ill... von Seri, Marco, Pecci, Alessandro, Di Bari, Filomena, Cusano, Roberto, Savino, Maria, Panza, Emanuele, Nigro, Alessandra, Noris, Patrizia, Gangarossa, Simone, Rocca, Bianca, Gresele, Paolo, Bizzaro, Nicola, Malatesta, Paola, Koivisto, Pasi A, Longo, Ilaria, Musso, Roberto, Pecoraro, Carmine, Iolascon, Achille, Magrini, Umberto, Rodriguez Soriano, Juan, Renieri, Alessandra, Ghiggeri, Gian Marco, Ravazzolo, Roberto, Balduini, Carlo L, Savoia, Anna

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Lipopolysaccharide Downregulates Fatty Acid Amide Hydrolase Expression and Increases Anandamide Levels in Human Peripheral Lymphocytes von Maccarrone, Mauro, De Petrocellis, Luciano, Bari, Monica, Fezza, Filomena, Salvati, Simona, Di Marzo, Vincenzo, Finazzi-Agrò, Alessandro

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