Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Pamela Cassini"'
Autor:
Claudio Rapezzi, Eloisa Arbustini, Manuela Agozzino, Maurizio Melis, Filippo Mangione, Annarita Colucci, Alexandra Smirnova, Riccardo Borroni, Elena Biagini, M Molinaro, Jagat Narula, Maurizia Rasura, Valentina Favalli, Alessandra Serio, Nupoor Narula, Antonello Ganau, Daniela Concolino, Maria Teresa Di Mascio, Antonia Nucera, GianPietro Sechi, Clelia Caspani, Camilla Vassallo, Carlo Pellegrini, Eliana Disabella, Umberto Scoditti, Marilena Tagliani, Calogero Giordano, Pamela Cassini, Massimiliano Marini, Carmela Giorgianni, Elena Antoniazzi, Anna Scarabotto, Donata Guidetti, Takahide Kodama, Marina Diomedi, Michelangelo Mancuso, Danilo Toni, Marialuisa Zedde, Luigi Tavazzi, Maurizia Grasso, Laura Scelsi, Lorenzo Giuliani, Laura Fancellu, Stefania Piga, Monica Concardi, Stefano Ghio
Publikováno v:
Journal of the American College of Cardiology. 68:1037-1050
Anderson-Fabry disease (AFD) is a rare X-linked lysosomal storage disease, caused by defects of the alpha-galactosidase A (GLA) gene. AFD can affect the heart, brain, kidney, eye, skin, peripheral nerves, and gastrointestinal tract. Cardiology (hyper
Autor:
Stefano Pizzolito, Pamela Cassini, Ilaria Chiaranda, Eloisa Arbustini, Nicola Marziliano, Lorenzo Magrassi, Miran Skrap, C. Arienta, Frediano Inzani
Publikováno v:
Cancer Letters. 290:36-42
By qPCR we found that EDG3 and SHC3 were amplified in 60% of ependymomas but none in choroid plexus papillomas. In ependymomas EDG3 and SHC3 amplification increased Shc3 protein levels while EDG3 was less affected. Both proteins were co-immunoprecipi
Autor:
Walter Borsini, Angelo Pirisi, Ilaria Romani, Gian Pietro Sechi, Anna Scarabotto, Rita Demurtas, Giovanni A. Deiana, Eloisa Arbustini, Elia Sechi, Pietro Emiliano Doneddu, A.L. Rassu, Pamela Cassini, Laura Fancellu
Publikováno v:
BMC Neurology
Background The etiologic determinants of stroke in young adults remain a diagnostic challenge in up to one-fourth of cases. Increasing evidences led to consider Fabry’s disease (FD) as a possible cause to check up. We aimed at evaluating the preval
Autor:
Tetsuo Hori, Leif Andersson, Alberto Montironi, Pamela Cassini, Sara Botti, Haruo Okhawa, Alessandra Stella, Elisabetta Giuffra
Publikováno v:
Mammalian Genome. 16:164-170
Anal atresia is a relatively common congenital malformation that occurs in about 1 out of 5000 infants, caused by abnormal hindgut development of the embryo, often associated with other developmental anomalies (e.g., Currarino, Townes-Brock, Palliste
Publikováno v:
Mycopathologia. 149:123-129
A respiratory syndrome very similar to extrinsic allergic alveolitis due to Penicillium verrucosum was recognized in 4 workers employed in a Gorgonzola cheese factory. A mycogen allergy to P. verrucosum, used as starter in the production, was demonst
Autor:
Eloisa, Arbustini, Andrea, Pilotto, Maurizia, Grasso, Nicola, Marziliano, Alessandra, Serio, Fabiana, Gambarin, Michele, Pasotti, Elena, Serafini, Pamela, Cassini, Barbara, Digiorgio
Publikováno v:
Human genetics. 125(3)
Autor:
Michele Pasotti, Alessandra Serio, Andrea Pilotto, Elena Serafini, Maurizia Grasso, Nicola Marziliano, Marilena Tagliani, Pamela Cassini, Barbara Digiorgio, Manuela Agozzino, Carlo Campana, Fabiana Gambarin, Stefano Ghio, Mario Viganò, Luigi Tavazzi, Eloisa Arbustini
Publikováno v:
Circulation. 118
Purpose To analyze the cardiac phenotype and long-term follow-up of dilated cardiolaminopathies. Lamin A/C (LMNA) gene mutations cause a variety of phenotypes. In the cardiologic setting, patients diagnosed with idiopathic dilated cardiomyopathy (DCM
Autor:
Pamela Cassini, Lorenzo Magrassi, Marco Marchionni, C. Arienta, Andrea Lanterna, Elena Cattaneo, Luciano Conti, Chiara Zuccato
Publikováno v:
Oncogene. 24(33)
A selective switch from expression of Shc1 gene to Shc3 occurs with maturation of neuronal precursors into postmitotic neurons. Previous studies showed that in the embryo, Shc1 is maximally expressed in dividing CNS stem cells while it is silenced in