Unexplained infertility and inherited thrombophilia von Bianca, S., M.D., Ph.D, Barrano, B., M.D., Ph.D, Cutuli, N., M.D, Indaco, L., M.D, Cataliotti, A., M.D, Milana, G., M.D, Barone, C., M.D, Ettore, G., M.D

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Hereditary haemorrhagic telangiectasia and genetic thrombophilia von Bianca, S, Cutuli, N, Bianca, M, Barrano, B, Cataliotti, A, Barone, C, Indaco, L, Milana, G

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Prenatal Diagnosis of Androgen Insensitivity Syndrome von Bianca, S., Cataliotti, A., Bartoloni, G., Torrente, I., Barrano, B., Boemi, G., Lo Presti, M., Indaco, L., Barone, C., Ettore, G.

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Recurrent pregnancy loss and inherited thrombophilia: who should be tested? von Bianca, S, Barrano, B, Cutuli, N, Indaco, L, Ingegnosi, C, Cataliotti, A, Milana, G, Ettore, G

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Hereditary haemorrhagic telangiectasia and genetic thrombophilia: Letter von Bianca, S, Cutuli, N, Bianca, M, Barrano, B, Cataliotti, A, Barone, C, Indaco, L, Milana, G

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Plasma Homocysteine Is Not Involved in the Thrombotic Risk of β-Thalassemia major Patients von Barrano, Barbara, Bertrand, Giuliano, Isaja, Teresa, Curreri, Roberto, Musumeci, Salvatore

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Hyperphenylalaninemia and birth weight von Bianca, Sebastiano, Meli, Concetta, Barrano, Barbara, Mollica, Florindo

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AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders von Valente, Enza Maria, Brancati, Francesco, Silhavy, Jennifer L., Castori, Marco, Marsh, Sarah E., Barrano, Giuseppe, Bertini, Enrico, Boltshauser, Eugen, Zaki, Maha S., Abdel-Aleem, Alice, Abdel-Salam, Ghada M. H., Bellacchio, Emanuele, Battini, Roberta, Cruse, Robert P., Dobyns, William B., Krishnamoorthy, Kalpathy S., Lagier-Tourenne, Clotilde, Magee, Alex, Pascual-Castroviejo, Ignacio, Salpietro, Carmelo D., Sarco, Dean, Dallapiccola, Bruno, Gleeson, Joseph G.

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Long-Term Clinical and Angiographic Results of Sirolimus-Eluting Stent in Complex Coronary Chronic Total Occlusion Revascularization: The SECTOR Registry von GALASSI, ALFREDO R., TOMASELLO, SALVATORE D., COSTANZO, LUCA, CAMPISANO, MARIA B., BARRANO, GIOMBATTISTA, TAMBURINO, CORRADO

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Does Occlusion Duration Influence Procedural and Clinical Outcome of Patients Who Underwent Percutaneous Coronary Intervention for Chronic Total Occlusion? von TOMASELLO, SALVATORE D., COSTANZO, LUCA, CAMPISANO, MARIA B., BARRANO, GIOMBATTISTA, CAPODANNO, DAVIDE, TAMBURINO, CORRADO, GALASSI, ALFREDO R.

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Long-Term Clinical and Angiographic Results of Sirolimus-Eluting Stent in Complex Coronary Chronic Total Occlusion Revascularization: The SECTOR Registry: SIROLIMUS ELUTING STENT I... von GALASSI, ALFREDO R., TOMASELLO, SALVATORE D., COSTANZO, LUCA, CAMPISANO, MARIA B., BARRANO, GIOMBATTISTA, TAMBURINO, CORRADO

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DMO03 CEP290 mutations are a frequent cause of Joubert syndrome with oculo-renal involvement von Valente, E.M, Brancati, F, Barrano, G, Silhavy, J.L, Marsh, S.E, Bertini, E, Boltshauser, E, Dallapiccola, B, Gleeson, J.G

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AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders von Valente, Enza Maria, Brancati, Francesco, Silhavy, Jennifer L, Castori, Marco, Marsh, Sarah E, Barrano, Giuseppe, Bertini, Enrico, Boltshauser, Eugen, Zaki, Maha S, Abdel-Aleem, Alice, Abdel-Salam, Ghada MH, Bellacchio, Emanuele, Battini, Roberta, Cruse, Robert P, Dobyns, William B, Krishnamoorthy, Kalpathy S, Lagier-Tourenne, Clotilde, Magee, Alex, Pascual-Castroviejo, Ignacio, Salpietro, Carmelo D, Sarco, Dean, Dallapiccola, Bruno, Gleeson, Joseph G

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