Knee arthroplasty system with medialized keel: Seven-year follow-up of a pioneer cohort von Benazzo, F., Jannelli, E., Ivone, A., Formagnana, M., Rossi, S.M., Ghiara, M., Danesino, G., Mosconi, M.

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Color Doppler ultrasonography of the abdominal aorta von Battaglia, S., Danesino, G.M., Danesino, V., Castellani, S.

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Overload syndromes of the knee in adolescents: Sonographic findings von Draghi, F., Danesino, G.M., Coscia, D., Precerutti, M., Pagani, C.

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Hepatic sonography in patients with hereditary hemorrhagic telangiectasia hospitalized for epistaxis von Draghi, F., Presazzi, A., Danesino, G.M., de Matthaeis, N., Rapaccini, G.L., Danesino, C.

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Pilomatricoma: Sonographic features von Garioni, E., Danesino, G.M., Madonia, L.

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Ultrasound of the elbow: Examination techniques and US appearance of the normal and pathologic joint von Draghi, F., Danesino, G.M., de Gautard, R., Bianchi, S.

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Scrotal pain as the first clinical manifestation of testicular seminoma: A case report von Baletti, A., Alessi, S., Danesino, G.M.

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Vascular abnormalities in the fingers of patients affected with hereditary hemorrhagic telangiectasia (HHT) as assessed by color doppler sonography von Draghi, F., Olivieri, C., Precerutti, M., Danesino, G.M., Pagella, F., Lanzarini, L., Semino, L., Valacca, C., Buscarini, E., Danesino, C.

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Palmar and finger varicosities: Presentation of a case von Battaglia, S., Danesino, G.M., Draghi, F.

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Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus von Grandis, M, Obici, L, Luigetti, M, Briani, C, Benedicenti, F, Bisogni, G, Canepa, M, Cappelli, F, Danesino, C, Fabrizi, G M, Fenu, S, Ferrandes, G, Gemelli, C, Manganelli, F, Mazzeo, A, Melchiorri, L, Perfetto, F, Pradotto, L G, Rimessi, P, Tini, G, Tozza, S, Trevisan, L, Pareyson, D, Mandich, P

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LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population von Musumeci, O, la Marca, G, Spada, M, Mondello, S, Danesino, C, Comi, G P, Pegoraro, E, Antonini, G, Marrosu, G, Liguori, R, Morandi, L, Moggio, M, Massa, R, Ravaglia, S, Di Muzio, A, Filosto, M, Tonin, P, Di Iorio, G, Servidei, S, Siciliano, G, Angelini, C, Mongini, T, Toscano, A

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Nasal powders of thalidomide for local treatment of nose bleeding in persons affected by hereditary hemorrhagic telangiectasia von Colombo, G., Bortolotti, F., Chiapponi, V., Buttini, F., Sonvico, F., Invernizzi, R., Quaglia, F., Danesino, C., Pagella, F., Russo, P., Bettini, R., Colombo, P., Rossi, A.

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Characterization of a mutation in the zona pellucida module of Endoglin that causes Hereditary Hemorrhagic Telangiectasia von Ruiz-Llorente, Lidia, Chiapparino, Elisa, Plumitallo, Sara, Danesino, Cesare, Bayrak-Toydemir, Pinar, Pagella, Fabio, Manfredi, Guido, Bernabeu, Carmelo, Jovine, Luca, Olivieri, Carla

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Mining the Plasma Proteome for Insights into the Molecular Pathology of Pulmonary Arterial Hypertension von Harbaum, Lars, Rhodes, Christopher J, Wharton, John, Lawrie, Allan, Karnes, Jason H, Desai, Ankit A, Nichols, William C, Humbert, Marc, Montani, David, Girerd, Barbara, Sitbon, Olivier, Boehm, Mario, Novoyatleva, Tatyana, Schermuly, Ralph T, Ghofrani, H Ardeschir, Toshner, Mark, Kiely, David G, Howard, Luke S, Swietlik, Emilia M, Gräf, Stefan, Pietzner, Maik, Morrell, Nicholas W, Wilkins, Martin R

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Diagnosis of glycogenosis type II von BEMBI, B, CERINI, E, TOSCANO, A, VIANELLO, A, DANESINO, C, DONATI, M. A, GASPERINI, S, MORANDI, L, MUSUMECI, O, PARENTI, G, RAVAGLIA, S, SEIDITA, F

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Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations von Villa, R., Fergnani, V.G.C., Silipigni, R., Guerneri, S., Cinnante, C., Guala, A., Danesino, C., Scola, E., Conte, G., Fumagalli, M., Gangi, S., Colombo, L., Picciolini, O., Ajmone, P.F., Accogli, A., Madia, F., Tassano, E., Scala, M., Capra, V., Srour, M., Spaccini, L., Righini, A., Greco, D., Castiglia, L., Romano, C., Bedeschi, M.F.

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Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network von Lesca, Gaëtan, Olivieri, Carla, Burnichon, Nelly, Pagella, Fabio, Carette, Marie-France, Gilbert-Dussardier, Brigitte, Goizet, Cyril, Roume, Joelle, Rabilloud, Muriel, Saurin, Jean-Christophe, Cottin, Vincent, Honnorat, Jerome, Coulet, Florence, Giraud, Sophie, Calender, Alain, Danesino, Cesare, Buscarini, Elisabetta, Plauchu, Henri

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A proportion of patients with lymphoma may harbor mutations of the perforin gene von Clementi, Rita, Locatelli, Franco, Dupré, Loïc, Garaventa, Alberto, Emmi, Lorenzo, Bregni, Marco, Cefalo, Graziella, Moretta, Antonia, Danesino, Cesare, Comis, Margherita, Pession, Andrea, Ramenghi, Ugo, Maccario, Rita, Aricò, Maurizio, Roncarolo, Maria Grazia

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Management and treatment of glycogenosis type II von BEMBI, B, CERINI, E, TOSCANO, A, VIANELLO, A, DANESINO, C, DONATI, M. A, GASPERINI, S, MORANDI, L, MUSUMECI, O, PARENTI, G, RAVAGLIA, S, SEIDITA, F

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The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome von Minelli, A, Maserati, E, Nicolis, E, Zecca, M, Sainati, L, Longoni, D, Lo Curto, F, Menna, G, Poli, F, De Paoli, E, Cipolli, M, Locatelli, F, Pasquali, F, Danesino, C

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