Alport syndrome: impact of digenic inheritance in patients management von Fallerini, C., Baldassarri, M., Trevisson, E., Morbidoni, V., La Manna, A., Lazzarin, R., Pasini, A., Barbano, G., Pinciaroli, A.R., Garosi, G., Frullanti, E., Pinto, A.M., Mencarelli, M.A., Mari, F., Renieri, A., Ariani, F.

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Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant) von Renieri, A, Mari, F, Mencarelli, M.A, Scala, E, Ariani, F, Longo, I, Meloni, I, Cevenini, G, Pini, G, Hayek, G, Zappella, M

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Early-onset seizure variant of Rett syndrome: Definition of the clinical diagnostic criteria von Artuso, R, Mencarelli, M.A, Polli, R, Sartori, S, Ariani, F, Pollazzon, M, Marozza, A, Cilio, M.R, Specchio, N, Vigevano, F, Vecchi, M, Boniver, C, Dalla Bernardina, B, Parmeggiani, A, Buoni, S, Hayek, G, Mari, F, Renieri, A, Murgia, A

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Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation von Bijlsma, E.K, Collins, A, Papa, F.T, Tejada, M.I, Wheeler, P, Peeters, E.A.J, Gijsbers, A.C.J, van de Kamp, J.M, Kriek, M, Losekoot, M, Broekma, A.J, Crolla, J.A, Pollazzon, M, Mucciolo, M, Katzaki, E, Disciglio, V, Ferreri, M.I, Marozza, A, Mencarelli, M.A, Castagnini, C, Dosa, L, Ariani, F, Mari, F, Canitano, R, Hayek, G, Botella, M.P, Gener, B, Mínguez, M, Renieri, A, Ruivenkamp, C.A.L

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2q24–q31 Deletion: Report of a case and review of the literature von Pescucci, C, Caselli, R, Grosso, S, Mencarelli, M.A, Mari, F, Farnetani, M.A, Piccini, B, Artuso, R, Bruttini, M, Priolo, M, Zuffardi, O, Gimelli, S, Balestri, P, Renieri, A

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A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb von Pollazzon, M, Grosso, S, Papa, F.T, Katzaki, E, Marozza, A, Mencarelli, M.A, Uliana, V, Balestri, P, Mari, F, Renieri, A

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CKAP2L mutation confirms the diagnosis of Filippi syndrome von Capecchi, G., Baldassarri, M., Ferranti, S., Guidoni, E., Cioni, M., Nürnberg, P., Mencarelli, M.A., Renieri, A., Grosso, S.

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A 2.6 Mb deletion of 6q24.3–25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears von Caselli, R, Mencarelli, M.A, Papa, F.T, Uliana, V, Schiavone, S, Strambi, M, Pescucci, C, Ariani, F, Rossi, V, Longo, I, Meloni, I, Renieri, A, Mari, F

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Non-collagen genes role in digenic Alport syndrome von Daga, S, Fallerini, C, Furini, S, Pecoraro, C, Scolari, F, Ariani, F, Bruttini, M, Mencarelli, M A, Mari, F, Renieri, A, Pinto, A M

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9q31.1q31.3 deletion in two patients with similar clinical features: A newly recognized microdeletion syndrome? von Mucciolo, M., Magini, P., Marozza, A., Mongelli, P., Mencarelli, M.A., Hayek, G., Tavalazzi, F., Mari, F., Seri, M., Renieri, A., Graziano, C.

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A 9.3Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb von Pollazzon, M., Grosso, S., Papa, F.T., Katzaki, E., Marozza, A., Mencarelli, M.A., Uliana, V., Balestri, P., Mari, F., Renieri, A.

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The Italian XLMR bank: a clinical and molecular database von Pescucci, C., Caselli, R., Mari, F., Speciale, C., Ariani, F., Bruttini, M., Sampieri, K., Mencarelli, M.A., Scala, E., Longo, I., Artuso, R., Renieri, A., Meloni, I.

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A 2.6Mb deletion of 6q24.3–25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears von Caselli, R., Mencarelli, M.A., Papa, F.T., Uliana, V., Schiavone, S., Strambi, M., Pescucci, C., Ariani, F., Rossi, V., Longo, I., Meloni, I., Renieri, A., Mari, F.

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Non-collagen genes role in digenic Alport syndrome von Daga, S, Fallerini, C, Furini, S, Pecoraro, C, Scolari, F, Ariani, F, Bruttini, M, Mencarelli, M.A, Mari, F, Renieri, A, Pinto, A.M

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Effects of expected perturbations on the velocity control of fast arm abduction movements von Pantaleo, T., Benvenuti, F., Bandinelli, S., Mencarelli, M.A., Baroni, A.

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Successful breeding predicts divorce in plovers von Halimubieke, N, Kupán, K, Valdebenito, J.O, Kubelka, V, Carmona-Isunza, M.C, Burgas, D, Catlin, D, St Clair, J.J.H, Cohen, J, Figuerola, J, Yasué, M, Johnson, M, Mencarelli, M, Cruz-López, M, Stantial, M, Weston, M.A, Lloyd, P, Que, P, Montalvo, T, Bansal, U, McDonald, G.C, Liu, Y, Kosztolányi, A, Székely, T

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