Alport syndrome: impact of digenic inheritance in patients management
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.
Published in Clinical genetics (01.07.2017)
Published in Clinical genetics (01.07.2017)
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Journal Article
Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases
Fallerini, C., Dosa, L., Tita, R., Del Prete, D., Feriozzi, S., Gai, G., Clementi, M., La Manna, A., Miglietti, N., Mancini, R., Mandrile, G., Ghiggeri, G.M., Piaggio, G., Brancati, F., Diano, L., Frate, E., Pinciaroli, A.R., Giani, M., Castorina, P., Bresin, E., Giachino, D., De Marchi, M., Mari, F., Bruttini, M., Renieri, A., Ariani, F.
Published in Clinical genetics (01.09.2014)
Published in Clinical genetics (01.09.2014)
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Journal Article
Non-collagen genes role in digenic Alport syndrome
Daga, S, Fallerini, C, Furini, S, Pecoraro, C, Scolari, F, Ariani, F, Bruttini, M, Mencarelli, M A, Mari, F, Renieri, A, Pinto, A M
Published in BMC nephrology (26.02.2019)
Published in BMC nephrology (26.02.2019)
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Journal Article
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes
Baldassarri, Margherita, Zguro, Kristina, Tomati, Valeria, Pastorino, Cristina, Fava, Francesca, Croci, Susanna, Bruttini, Mirella, Picchiotti, Nicola, Furini, Simone, Pedemonte, Nicoletta, Gabbi, Chiara, Renieri, Alessandra, Fallerini, Chiara
Published in Cells (Basel, Switzerland) (16.12.2022)
Published in Cells (Basel, Switzerland) (16.12.2022)
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