Acquired lecithin:cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney disease von Calabresi, L., Simonelli, S., Conca, P., Busnach, G., Cabibbe, M., Gesualdo, L., Gigante, M., Penco, S., Veglia, F., Franceschini, G.

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Antitumor efficacy of the heparanase inhibitor SST0001 alone and in combination with antiangiogenic agents in the treatment of human pediatric sarcoma models von Cassinelli, G., Lanzi, C., Tortoreto, M., Cominetti, D., Petrangolini, G., Favini, E., Zaffaroni, N., Pisano, C., Penco, S., Vlodavsky, I., Zunino, F.

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Mutations of FUS gene in sporadic amyotrophic lateral sclerosis von Corrado, Lucia, Del Bo, Roberto, Castellotti, Barbara, Ratti, Antonia, Cereda, Cristina, Penco, Silvana, Sorarù, Gianni, Carlomagno, Yari, Ghezzi, Serena, Pensato, Viviana, Colombrita, Claudia, Gagliardi, Stella, Cozzi, Lorena, Orsetti, Valeria, Mancuso, Michelangelo, Siciliano, Gabriele, Mazzini, Letizia, Comi, Giacomo Pietro, Gellera, Cinzia, Ceroni, Mauro, D'Alfonso, Sandra, Silani, Vincenzo

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Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis von Tarlarini, C., Lunetta, C., Mosca, L., Avemaria, F., Riva, N., Mantero, V., Maestri, E., Quattrini, A., Corbo, M., Melazzini, M. G., Penco, S.

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Factors affecting formation and rupture of intracranial saccular aneurysms von Bacigaluppi, S., Piccinelli, M., Antiga, L., Veneziani, A., Passerini, T., Rampini, P., Zavanone, M., Severi, P., Tredici, G., Zona, G., Krings, T., Boccardi, E., Penco, S., Fontanella, M.

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Genetic and phenotypic characterization of LDL-receptor in patients with a clinical diagnosis of familial hypercholesterolemia: Two novel mutations von Pavanello, C, Tarlarini, C, Penco, S, Calabresi, L, Castelnuovo, S, Mombelli, G, Sirtori, C

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Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management von Bacigaluppi, S, Retta, SF, Pileggi, S, Fontanella, M, Goitre, L, Tassi, L, La Camera, A, Citterio, A, Patrosso, MC, Tredici, G, Penco, S

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Lipoprotein (a): concentration, isoforms, polymorphisms and association with preclinical atherosclerosis von Pavanello, C, Vitali, C, Tarlarini, C, Penco, S, Calabresi, L, Mombelli, G, Sirtori, C.R

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Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld–Rieger syndrome and glaucoma von Pasutto, F., Mauri, L., Popp, B., Sticht, H., Ekici, A., Piozzi, E., Bonfante, A., Penco, S., Schlötzer-Schrehardt, U., Reis, A.

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Cataract and optic disk drusen in a patient with glycogenosis and di George syndrome: clinical and molecular report von Allegrini, D, Penco, S, Pece, A, Autelitano, A, Montesano, G, Paci, S, Montanari, C, Maver, A, Peterlin, B, Damante, G, Rossetti, L

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Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosis von Cozzi, L., Campolo, J., Parolini, M., De Maria, R., Patrosso, M. C., Marocchi, A., Parodi, O., Penco, S.

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Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype von Lunetta, C., Sansone, V. A., Penco, S., Mosca, L., Tarlarini, C., Avemaria, F., Maestri, E., Melazzini, M. G., Meola, G., Corbo, M.

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A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas von Cigoli, M. S., De Benedetti, S., Marocchi, A., Bacigaluppi, S., Primignani, P., Gesu, G., Citterio, A., Tassi, L., Mecarelli, O., Pulitano, P., Penco, S.

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Erratum to: Underestimation rate of lobular intraepithelial neoplasia in vacuum-assisted breast biopsy von Meroni, S., Bozzini, A. C., Pruneri, G., Moscovici, O. C., Maisonneuve, P., Menna, S., Penco, S., Meneghetti, L., Renne, G., Cassano, E.

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Epidemiological Characteristics Of Patients With Recent Diagnosis Of HIV In A Referral Center von Tortone, N., Penco, S.

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Interactions of fibroblasts with soldered and laser-welded joints von Solmi, R., Martini, D., Zanarini, M., Isaza Penco, S., Rimondini, L., Carinci, P., Borea, G., Ruggeri, A.

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Novel 7-Oxyiminomethyl Derivatives of Camptothecin with Potent in Vitro and in Vivo Antitumor Activity von Dallavalle, Sabrina, Ferrari, Anna, Biasotti, Barbara, Merlini, Lucio, Penco, Sergio, Gallo, Grazia, Marzi, Mauro, Tinti, Maria Ornella, Martinelli, Roberta, Pisano, Claudio, Carminati, Paolo, Carenini, Nives, Beretta, Giovanni, Perego, Paola, De Cesare, Michelandrea, Pratesi, Graziella, Zunino, Franco

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RAR‐specific agonist/antagonists which dissociate transactivation and AP1 transrepression inhibit anchorage‐independent cell proliferation von Chen, J.Y., Penco, S., Ostrowski, J., Balaguer, P., Pons, M., Starrett, J.E., Reczek, P., Chambon, P., Gronemeyer, H.

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Antioxidant activity of timolol on endothelial cells and its relevance for glaucoma course von Izzotti, A, Saccà, S C, Di Marco, B, Penco, S, Bassi, A M

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ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations von Gianfrancesco, F, Esposito, T, Penco, S, Maglione, V, Liquori, C.L, Patrosso, M.C, Zuffardi, O, Ciccodicola, A, Marchuk, D.A, Squitieri, F

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