CARDANI, ROSANNA
CARDANI, ROSANNA
DIPARTIMENTO DI SCIENZE MEDICO-CHIRURGICHE (attivo dal 01/01/2003 al 27/04/2012)
A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1
2008 R. Cardani, E. Mancinelli, G. Saino, L. Bonavina, G. Meola
Antibody responses to BNT162b2 mRNA vaccine: infection‐naïve individuals with abdominal obesity warrant attention
2021 A.E. Malavazos, S. Basilico, G. Iacobellis, V. Milani, R. Cardani, F. Boniardi, C. Dubini, I. Prandoni, G. Capitanio, L.V. Renna, S. Boveri, R. Rigolini, M. Carrara, G. Spuria, T. Cuppone, A. D’Acquisto, L. Carpinelli, M. Sacchi, L. Morricone, F. Secchi, E. Costa, L. Menicanti, E. Nisoli, M. Carruba, F. Ambrogi, M.M. Corsi Romanelli
Biomolecular diagnosis of myotonic dystrophy type 2 : a challenging approach
2017 G. Meola, F. Biasini, R. Valaperta, E. Costa, R. Cardani
Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy
2004 R. Cardani, E. Mancinelli, V. Sansone, G. Rotondo, G. Meola
BRAF V599E mutation occurs in Spitz and Reed nevi
2006 C. La Porta, R. Cardani, F. Facchetti, P. Presicce, S. Rao, E. Privitera, C. Clemente, M. C. Mihm
Characterization of sarcoplasmic reticulum Ca2+ ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy
2016 V. Guglielmi, A. Oosterhof, N.C. Voermans, R. Cardani, J.P. Molenaar, T.H. van Kuppevelt, G. Meola, B.G. van Engelen, G. Tomelleri, G. Vattemi
Circulating irisn is reduced in male patients with type 1 and type 2 Myotonic Dystrophies
2017 E. Dozio, E. Passeri, R. Cardani, S. Benedini, C. Aresta, R. Valaperta, M. Corsi Romanelli, G. Meola, V. Sansone, S. Corbetta
Clinical Reasoning : a 35-year-old woman with hyperstartling, stiffness, and accidental falls : a startling diagnosis
2017 S.P. Russo, B. Fossati, M. Toffetti, J. Lanzone, R. Cardani, G. Meola
Co-occurrence of DMPK expansion and CLCN1 mutation in a patient with myotonia
2021 S. Locci, R. Cardani, P. Brunori, S. Lucchiari, G.P. Comi, A. Federico, N. De Stefano, G. Meola, A. Mignarri
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2
2012 R. Cardani, M. Giagnacovo, A. Botta, F. Rinaldi, A. Morgante, B. Udd, O. Raheem, S. Penttilä, T. Suominen, L.V. Renna, V. Sansone, E. Bugiardini, G. Novelli, G. Meola
Colocalization of ribonuclear inclusions and MBNL1 foci with no impairment of muscle differentiation in DM2
2005 G. Meola, R. Cardani, E. Mancinelli, G. Rotondo
Development and validation of a new molecular diagnostic assay for detection of myotonic dystrophy type 2
2015 R. Valaperta, F. Lombardi, R. Cardani, B. Fossati, E. Brigonzi, I. Merli, V. Sansone, G. Merletti, E. Spina, G. Meola, E. Costa
Effect of glucose stress conditions in BL6T murine melanoma cells
2004 S. Cedrola, R. Cardani, C.A.M. La Porta
Establishment of a cardiac biobank in a Department of Pathology and Laboratory Medicine
2020 R. Cardani, E.G. Bertoldo, A. Cerri, M. Picozzi, M.M. Corsi Romanelli, E. Callus
Genome wide identification of aberrant alternative splicing events in myotonic dystrophy type 2
2014 A. Perfetti, S. Greco, P. Fasanaro, E. Bugiardini, R. Cardani, J.M. Garcia Manteiga, M. Riba, D. Cittaro, E. Stupka, G. Meola, F. Martelli
High-sensitive cardiac troponin T (hs-cTnT) assay as serum biomarker to predict cardiac risk in myotonic dystrophy : A case-control study
2016 R. Valaperta, M. Gaeta, R. Cardani, F. Lombardi, B. Rampoldi, C. De Siena, F. Mori, B. Fossati, P. Gaia, O.E. Ferraro, S. Villani, S. Iachettini, M. Piccoli, F. Cirillo, E. Pusineri, G. Meola, E. Costa
Muscleblind-like protein 1 nuclear sequestration and splicing pattern in myotonic dystrophy type 2
2006 R. Cardani, E. Mancinelli, A. Botta, G. Novelli, G. Meola
Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2
2006 R Cardani, E Mancinelli, G Rotondo, V Sansone, G Meola
Myotonic dystrophies : an update on clinical aspects, genetic, pathology, and molecular pathomechanisms
2015 G. Meola, R. Cardani
Myotonic dystrophy type 2 and modifier genes : an update on clinical and pathomolecular aspects
2017 G. Meola, R. Cardani