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Search Results - Prontera, Alessia
Search Results - Prontera, Alessia
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Una gravidanza 'blasfema' (Ennod. carm . 2.97 H. = 217 V.)
by
Prontera, Alessia
Published in
Lexis (Venezia, Online)
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Comparison of high‐sensitive cardiac troponin T and I in patients with chronic coronary syndrome
by
Caselli, Chiara
,
Ragusa, Rosetta
,
Liga, Riccardo
,
Prontera, Concetta
,
Gimelli, Alessia
,
Scholte, Arthur
,
Knuuti, Juhani
,
Clerico, Aldo
,
Neglia, Danilo
Published in
European journal of clinical investigation
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Mutation spectrum of MLL2 in a cohort of Kabuki syndrome patients
by
Micale, Lucia
,
Augello, Bartolomeo
,
Fusco, Carmela
,
Selicorni, Angelo
,
Loviglio, Maria N
,
Silengo, Margherita Cirillo
,
Reymond, Alexandre
,
Gumiero, Barbara
,
Zucchetti, Federica
,
D'Addetta, Ester V
,
Belligni, Elga
,
Calcagnì, Alessia
,
Digilio, Maria C
,
Dallapiccola, Bruno
,
Faravelli, Francesca
,
Forzano, Francesca
,
Accadia, Maria
,
Bonfante, Aldo
,
Clementi, Maurizio
,
Daolio, Cecilia
,
Douzgou, Sofia
,
Ferrari, Paola
,
Fischetto, Rita
,
Garavelli, Livia
,
Lapi, Elisabetta
,
Mattina, Teresa
,
Melis, Daniela
,
Patricelli, Maria G
,
Priolo, Manuela
,
Prontera, Paolo
,
Renieri, Alessandra
,
Mencarelli, Maria A
,
Scarano, Gioacchino
,
della Monica, Matteo
,
Toschi, Benedetta
,
Turolla, Licia
,
Vancini, Alessandra
,
Zatterale, Adriana
,
Gabrielli, Orazio
,
Zelante, Leopoldo
,
Merla, Giuseppe
Published in
Orphanet journal of rare diseases
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Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying NSD1 Variants
by
Ferilli, Marco
,
Ciolfi, Andrea
,
Pedace, Lucia
,
Niceta, Marcello
,
Radio, Francesca Clementina
,
Pizzi, Simone
,
Miele, Evelina
,
Cappelletti, Camilla
,
Mancini, Cecilia
,
Galluccio, Tiziana
,
Andreani, Marco
,
Iascone, Maria
,
Chiriatti, Luigi
,
Novelli, Antonio
,
Micalizzi, Alessia
,
Matraxia, Marta
,
Menale, Lucia
,
Faletra, Flavio
,
Prontera, Paolo
,
Pilotta, Alba
,
Bedeschi, Maria Francesca
,
Capolino, Rossella
,
Baban, Anwar
,
Seri, Marco
,
Mammì, Corrado
,
Zampino, Giuseppe
,
Digilio, Maria Cristina
,
Dallapiccola, Bruno
,
Priolo, Manuela
,
Tartaglia, Marco
Published in
Genes
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Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying INSD1/I Variants
by
Ferilli, Marco
,
Ciolfi, Andrea
,
Pedace, Lucia
,
Niceta, Marcello
,
Radio, Francesca Clementina
,
Pizzi, Simone
,
Miele, Evelina
,
Cappelletti, Camilla
,
Mancini, Cecilia
,
Galluccio, Tiziana
,
Andreani, Marco
,
Iascone, Maria
,
Chiriatti, Luigi
,
Novelli, Antonio
,
Micalizzi, Alessia
,
Matraxia, Marta
,
Menale, Lucia
,
Faletra, Flavio
,
Prontera, Paolo
,
Pilotta, Alba
,
Bedeschi, Maria Francesca
,
Capolino, Rossella
,
Baban, Anwar
,
Seri, Marco
,
Mammì, Corrado
,
Zampino, Giuseppe
,
Digilio, Maria Cristina
,
Dallapiccola, Bruno
,
Priolo, Manuela
,
Tartaglia, Marco
Published in
Genes
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GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease—study protocol and preliminary results
by
Bersano, Anna
,
Bedini, Gloria
,
Nava, Sara
,
Acerbi, Francesco
,
Sebastiano, Davide Rossi
,
Binelli, Simona
,
Franceschetti, Silvana
,
Faragò, Giuseppe
,
Grisoli, Marina
,
Gioppo, Andrea
,
Ferroli, Paolo
,
Bruzzone, Maria Grazia
,
Riva, Daria
,
Ciceri, Elisa
,
Pantaleoni, Chiara
,
Saletti, Veronica
,
Esposito, Silvia
,
Nardocci, Nardo
,
Zibordi, Federica
,
Caputi, Luigi
,
Marzoli, Stefania Bianchi
,
Zedde, Maria Luisa
,
Pavanello, Marco
,
Raso, Alessandro
,
Capra, Valeria
,
Pantoni, Leonardo
,
Sarti, Cristina
,
Pezzini, Alessandro
,
Caria, Filomena
,
Dell’ Acqua, Maria Luisa
,
Zini, Andrea
,
Baracchini, Claudio
,
Farina, Filippo
,
Sanguigni, Sandro
,
De Lodovici, Maria Luisa
,
Bono, Giorgio
,
Capone, Fioravanti
,
Di Lazzaro, Vincenzo
,
Lanfranconi, Silvia
,
Toscano, Massimiliano
,
Di Piero, Vittorio
,
Sacco, Simona
,
Carolei, Antonio
,
Toni, Danilo
,
Paciaroni, Maurizio
,
Caso, Valeria
,
Perrone, Patrizia
,
Calloni, Maria Vittoria
,
Romani, Alfredo
,
Cenzato, Marco
,
Fratianni, Alessia
,
Ciusani, Emilio
,
Prontera, Paolo
,
Lasserve, Elisabeth Tournier
,
Blecharz, Kinga
,
Vajkoczy, Peter
,
Parati, Eugenio Agostino
Published in
Neurological sciences
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N-terminal fragment of proBNP is a marker of high cardiac output cardiomyopathy evaluated by CMR in thalassemia syndromes
by
Meloni, Antonella
,
Pepe, Alessia
,
Zyw, Luc
,
Positano, Vincenzo
,
Dell'Amico, Maria Chiara
,
Prontera, Concetta
,
Passino, Claudio
,
Fabrizio, Filomena
,
Romeo, Maria Antonietta
,
Ein, Michele
,
Lombardi, Massimo
Published in
Journal of cardiovascular magnetic resonance
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