CARDANI, ROSANNA

CARDANI, ROSANNA  

DIPARTIMENTO DI SCIENZE MEDICO-CHIRURGICHE (attivo dal 01/01/2003 al 27/04/2012)  

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Risultati 1 - 20 di 34 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1 1-gen-2008 R. CardaniE. MancinelliL. BonavinaG. Meola + Article (author) -
Antibody responses to BNT162b2 mRNA vaccine: infection‐naïve individuals with abdominal obesity warrant attention 1-gen-2021 Malavazos, Alexis EliasBasilico, SaraCardani, RosannaBoniardi, FedericoRenna, Laura ValentinaCarrara, MatteoSpuria, GiovanniCuppone, TeresaCarpinelli, LucaSecchi, FrancescoCosta, ElenaNisoli, EnzoCarruba, MicheleAmbrogi, FedericoCorsi Romanelli, Massimiliano Marco + Article (author) -
Biomolecular diagnosis of myotonic dystrophy type 2 : a challenging approach 1-gen-2017 G. MeolaR. ValapertaE. CostaR. Cardani + Article (author) -
Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy 1-gen-2004 R. CardaniE. MancinelliV. SansoneG. Meola + Article (author) -
BRAF V599E mutation occurs in Spitz and Reed nevi 1-gen-2006 C. La PortaR. CardaniF. FacchettiP. PresicceE. Privitera + Article (author) -
Characterization of sarcoplasmic reticulum Ca2+ ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy 1-gen-2016 GUGLIELMI, VITTORIAR. CardaniG. Meola + Article (author) -
Circulating irisn is reduced in male patients with type 1 and type 2 Myotonic Dystrophies 14-nov-2017 E. DozioE. PasseriR. CardaniS. BenediniC. ArestaR. ValapertaM. Corsi RomanelliG. MeolaV. SansoneS. Corbetta Article (author) -
Clinical Reasoning : a 35-year-old woman with hyperstartling, stiffness, and accidental falls : a startling diagnosis 1-gen-2017 RUSSO, SILVIA PAOLAB. FossatiTOFFETTI, MAUROR. CardaniG. Meola + Article (author) -
Co-occurrence of DMPK expansion and CLCN1 mutation in a patient with myotonia 1-gen-2021 Cardani R.Lucchiari S.Comi G. P.Meola G. + Article (author) -
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2 1-ott-2012 R. CardaniL.V. RennaV. SansoneE. BugiardiniG. Meola + Article (author) -
Colocalization of ribonuclear inclusions and MBNL1 foci with no impairment of muscle differentiation in DM2 1-gen-2005 G. MeolaR. CardaniE. Mancinelli + Book Part (author) -
Development and validation of a new molecular diagnostic assay for detection of myotonic dystrophy type 2 1-gen-2015 R. ValapertaR. CardaniB. FossatiE. BrigonziI. MerliV. SansoneG. Meola + Article (author) -
Effect of glucose stress conditions in BL6T murine melanoma cells 1-gen-2004 S. CedrolaR. CardaniC.A.M. La Porta Article (author) -
Establishment of a cardiac biobank in a Department of Pathology and Laboratory Medicine 1-nov-2020 Cardani, RPicozzi, MCorsi Romanelli, M MCallus, E + Article (author) -
Genome wide identification of aberrant alternative splicing events in myotonic dystrophy type 2 10-apr-2014 A. PerfettiE. BugiardiniR. CardaniG. Meola + Article (author) -
High-sensitive cardiac troponin T (hs-cTnT) assay as serum biomarker to predict cardiac risk in myotonic dystrophy : A case-control study 1-dic-2016 R. ValapertaR. CardaniB. FossatiP. GaiaM. PiccoliF. CirilloG. Meola + Article (author) -
Muscleblind-like protein 1 nuclear sequestration and splicing pattern in myotonic dystrophy type 2 1-gen-2006 R. CARDANIE. MANCINELLIG. MEOLA + Article (author) -
Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2 1-gen-2006 R CardaniE MancinelliV SansoneG Meola + Article (author) -
Myotonic dystrophies : an update on clinical aspects, genetic, pathology, and molecular pathomechanisms 1-apr-2015 G. MeolaR. Cardani Article (author) -
Myotonic dystrophy type 2 and modifier genes : an update on clinical and pathomolecular aspects 1-apr-2017 G. MeolaR. Cardani Article (author) -