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Chrysanthos Grigoratos

affiliation not provided to SSRN

  • affiliation not provided to SSRN

SCHOLARLY PAPERS

2

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54

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Scholarly Papers (2)

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1.

Cardiac Magnetic Resonance Findings and Prognosis in Type 1 Myotonic Dystrophy

Number of pages: 22 Posted: 14 Mar 2022
Marco Leali, Alberto Aimo, Giulia Ricci, Francesca Torri, Giancarlo Todiere, Giuseppe Vergaro, Chrysanthos Grigoratos, Alberto Giannoni, Giovanni Donato Aquaro, Gabriele Siciliano, Michele Emdin, Claudio Passino and Andrea Barison
affiliation not provided to SSRN, Scuola Superiore Sant’Anna, affiliation not provided to SSRN, affiliation not provided to SSRN, Fondazione Toscana Gabriele Monasterio, affiliation not provided to SSRN, affiliation not provided to SSRN, Scuola Superiore Sant'Anna di Pisa, Fondazione Toscana Gabriele Monasterio, University of Pisa, Scuola Superiore Sant’Anna, Scuola Superiore Sant’Anna and affiliation not provided to SSRN
Downloads 34 (1,263,436)

Abstract:

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DM1, myotonic, Steinert, heart, CMR, magnetic resonance

2.

Dilated cardiomyopathy vs. non-dilated left ventricular dysfunction: genotype-phenotype relationship and outcome

Number of pages: 21 Posted: 12 Jan 2026
Irina Bellisario, Alberto Aimo, Giancarlo Todiere, Bianca Alderotti, Ignazio Alessio Gueli, Chrysanthos Grigoratos, Fabrizio Ricci, Carmelo De Gori, Matilda Muca, Nicoletta Botto, Simona Vittorini, Sabina Gallina, Claudio Passino, Michele Emdin, alberto Clemente and Andrea Barison
affiliation not provided to SSRN, Scuola Superiore Sant’Anna, Fondazione Toscana Gabriele Monasterio, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, University G. d’Annunzio of Chieti-Pescara, Scuola Superiore Sant'Anna di Pisa, Scuola Superiore Sant'Anna di Pisa, affiliation not provided to SSRN and affiliation not provided to SSRN
Downloads 20 (1,448,301)

Abstract:

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dilated cardiomyopathy, left ventricular dysfunction, late enhancement, gene mutations, prognosis