Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution von Piccirillo, S G M, Combi, R, Cajola, L, Patrizi, A, Redaelli, S, Bentivegna, A, Baronchelli, S, Maira, G, Pollo, B, Mangiola, A, DiMeco, F, Dalprà, L, Vescovi, A L

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Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation von Bodega, B., Bione, S., Dalprà, L., Toniolo, D., Ornaghi, F., Vegetti, W., Ginelli, E., Marozzi, Anna

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A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning von Villa, N, Conconi, D, Benussi, D Gambel, Tornese, G, Crosti, F, Sala, E, Dalprà, L, Pecile, V

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Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure von Marozzi, A., Porta, C., Vegetti, W., Crosignani, P.G., Tibiletti, M.G., Dalprà, L., Ginelli, E.

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APOE influences vasospasm and cognition of noncomatose patients with subarachnoid hemorrhage von LANTERNA, L. A, RIGOLDI, M, TREDICI, G, BIROLI, F, CESANA, C, GAINI, S. M, DALPRA, L

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Autosomal dominant nocturnal frontal lobe epilepsy. A critical overview von COMBI, Romina, DALPRA, Leda, TENCHINI, Maria Luisa, FERINI-STRAMBI, Luigi

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Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 von Novelli, A., Grati, F. R., Ballarati, L., Bernardini, L., Bizzoco, D., Camurri, L., Casalone, R., Cardarelli, L., Cavalli, P., Ciccone, R., Clementi, M., Dalprà, L., Gentile, M., Gelli, G., Grammatico, P., Malacarne, M., Nardone, A. M., Pecile, V., Simoni, G., Zuffardi, O., Giardino, D.

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Clinical and genetic evaluation of a family showing both autism and epilepsy von Combi, R, Redaelli, S, Beghi, M, Clerici, M, Cornaggia, C.M, Dalprà, L

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Association between idiopathic premature ovarian failure and fragile X premutation von Marozzi, Anna, Vegetti, Walter, Manfredini, Emanuela, Tibiletti, Maria Grazia, Testa, Giovanna, Crosignani, Pier Giorgio, Ginelli, Enrico, Meneveri, Raffaella, Dalprà, Leda

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The idiopathic forms of premature menopause and early menopause show the same genetic pattern von Tibiletti, M.G., Testa, G., Vegetti, W., Alagna, F., Taborelli, M., Dalprà, L., Bolis, P.F., Crosignani, P.G.

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Autosomal dominant nocturnal frontal lobe epilepsy: A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome von OLDANI, A, ZUCCONI, M, ASSELTA, R, MODUGNO, M, BONATI, M. T, DALPRA, L, MALCOVATI, M, TENCHINI, M. L, SMIRNE, S, FERINI-STRAMBI, L

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Age-related increase of baseline frequencies of sister chromatid exchanges, chromosome aberrations, and micronuclei in human lymphocytes von Bolognesi, C, Abbondandolo, A, Barale, R, Casalone, R, Dalprà, L, De Ferrari, M, Degrassi, F, Forni, A, Lamberti, L, Lando, C, Migliore, L, Padovani, P, Pasquini, R, Puntoni, R, Sbrana, I, Stella, M, Bonassi, S

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Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B von Bione, S., Rizzolio, F., Sala, C., Ricotti, R., Goegan, M., Manzini, M.C., Battaglia, R., Marozzi, A., Vegetti, W., Dalprà, L., Crosignani, P.G., Ginelli, E., Nappi, R., Bernabini, S., Bruni, V., Torricelli, F., Zuffardi, O., Toniolo, D.

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Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure von MAROZZI, Anna, MANFREDINI, Emanuela, TIBILETTI, Maria Grazia, FURLAN, Daniela, VILLA, Nicoletta, VEGETTI, Walter, CROSIGNANI, Pier Giorgio, GINELLI, Enrico, MENEVERI, Raffaella, DALPRA, Leda

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Relationship between clinical and genetic features in “inverted duplicated chromosome 15” patients von Borgatti, Renato, Piccinelli, Paolo, Passoni, Davide, Dalprà, Leda, Miozzo, Monica, Micheli, Roberto, Gagliardi, Chiara, Balottin, Umberto

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A tumor suppressor locus in familial and sporadic chordoma maps to 1p36 von Miozzo, Monica, Dalprà, Leda, Riva, Paola, Volontà, Marinella, Macciardi, Fabio, Pericotti, Sergio, Tibiletti, M. Grazia, Cerati, Michele, Rohde, Klaus, Larizza, Lidia, Fuhrman Conti, A. Maria

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Premature ovarian failure von Vegetti, Walter, Marozzi, Anna, Manfredini, Emanuela, Testa, Giovanna, Alagna, Federica, Nicolosi, Annaelisa, Caliari, Ilaria, Taborelli, Monica, Tibiletti, Maria Grazia, Dalprà, Leda, Crosignani, Pier Giorgio

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Interstitial telomeres of an inv(9)(p11.2;q34) involved in a jumping translocation found in a woman through a stable unbalanced translocation in her malformed child von Sala, E, Villa, N, Riva, P, Varisco, T, Larizza, L, Dalprà, L

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Anxiolytic effect of clonazepam in female rats: Grooming microstructure and elevated plus maze tests von Nin, Maurício S., Couto-Pereira, Natividade S., Souza, Marilise F., Azeredo, Lucas A., Ferri, Marcelo K., Dalprá, Walesca L., Gomez, Rosane, Barros, Helena M.T.

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Monosomy and trisomy 1q44-qter in two sisters originating from a half cryptic 1q;15p translocation von VILLA, NICOLETTA, SALA, ELENA, COLOMBO, DANIELA, DELL'ORTO, MARIAGRAZIA, GRIONI, DANIELE, DALPRÀ, LEDA

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