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Search Results - SAVASTA, CARLO
Search Results - SAVASTA, CARLO
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Severe Spontaneous Echo Contrast/Auricolar Thrombosis in “Nonvalvular” AF: Value of Thromboembolic Risk Scores
by
MASCIOLI, GIOSUÈ
,
LUCCA, ELENA
,
MICHELOTTI, FEDERICA
,
ALIOTO, GIUSY
,
SANTORO, FRANCO
,
BELLI, GUIDO
,
ROTA, CRISTINA
,
ORNAGO, OMBRETTA
,
SIRIANNI, GIOVANNI
,
PULCINI, EMANUELA
,
PENNESI, MATTEO
,
SAVASTA, CARLO
,
RUSSO, ROSARIO
,
PITÌ, ANTONINO
Published in
Pacing and clinical electrophysiology
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Emergency percutaneous coronary intervention in patients with ST-elevation myocardial infarction complicated by out-of-hospital cardiac arrest: Early and medium-term outcome
by
Lettieri, Corrado, MD
,
Savonitto, Stefano, MD
,
De Servi, Stefano, MD
,
Guagliumi, Giulio, MD
,
Belli, Guido, MD
,
Repetto, Alessandra, MD
,
Piccaluga, Emanuela, MD
,
Politi, Alessandro, MD
,
Ettori, Federica, MD
,
Castiglioni, Battistina, MD
,
Fabbiocchi, Franco, MD
,
De Cesare, Nicoletta, MD
,
Sangiorgi, Giuseppe, MD
,
Musumeci, Giuseppe, MD
,
Onofri, Marco, MD
,
D'Urbano, Maurizio, MD
,
Pirelli, Salvatore, MD
,
Zanini, Roberto, MD
,
Klugmann, Silvio, MD
Published in
The American heart journal
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The treatment of carotid artery bifurcation stenoses with systematic stenting: experience of first 100 consecutive cardiological procedures
by
Sganzerla, Paolo
,
Bocciarelli, Monica
,
Savasta, Carlo
,
Bonin, Monica
,
Tavasci, Emanuela
,
Fini, Matteo
,
Perlasca, Elena
,
Alioto, Giusy
,
Colombo, Francesca
,
Passaretti, Bruno
Published in
The Journal of invasive cardiology
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Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment
by
Salpietro, Vincenzo
,
Malintan, Nancy T.
,
Llano-Rivas, Isabel
,
Spaeth, Christine G.
,
Efthymiou, Stephanie
,
Striano, Pasquale
,
Vandrovcova, Jana
,
Cutrupi, Maria C.
,
Chimenz, Roberto
,
David, Emanuele
,
Di Rosa, Gabriella
,
Marce-Grau, Anna
,
Raspall-Chaure, Miquel
,
Martin-Hernandez, Elena
,
Zara, Federico
,
Minetti, Carlo
,
Salpietro, Vincenzo
,
Efthymiou, Stephanie
,
Kriouile, Yamna
,
El Khorassani, Mohamed
,
Aguennouz, Mhammed
,
Karashova, Blagovesta
,
Avdjieva, Daniela
,
Kathom, Hadil
,
Tincheva, Radka
,
Van Maldergem, Lionel
,
Nachbauer, Wolfgang
,
Boesch, Sylvia
,
Arning, Larissa
,
Timmann, Dagmar
,
Cormand, Bru
,
Pérez-Dueñas, Belen
,
Di Rosa, Gabriella
,
Pironti, Erica
,
Goraya, Jatinder S.
,
Sultan, Tipu
,
Kirmani, Salman
,
Ibrahim, Shahnaz
,
Jan, Farida
,
Mine, Jun
,
Banu, Selina
,
Veggiotti, Pierangelo
,
Ferrari, Michel D.
,
Verrotti, Alberto
,
Marseglia, Gian Luigi
,
Savasta, Salvatore
,
Garavaglia, Barbara
,
Scuderi, Carmela
,
Borgione, Eugenia
,
Dipasquale, Valeria
,
Cutrupi, Maria Concetta
,
Portaro, Simona
,
Sanchez, Benigno Monteagudo
,
Pineda-Marfa’, Mercedes
,
Munell, Francina
,
Macaya, Alfons
,
Boles, Richard
,
Heimer, Gali
,
Papacostas, Savvas
,
Manole, Andreea
,
Malintan, Nancy
,
Zanetti, Maria Natalia
,
Hanna, Michael G.
,
Rothman, James E.
,
Kullmann, Dimitri M.
,
Houlden, Henry
,
Bello, Oscar D.
,
De Zorzi, Rita
,
Fortuna, Sara
,
Dauber, Andrew
,
Alkhawaja, Mariam
,
Sultan, Tipu
,
Mankad, Kshitij
,
Vitobello, Antonio
,
Thomas, Quentin
,
Mau-Them, Frederic Tran
,
Faivre, Laurence
,
Martinez-Azorin, Francisco
,
Prada, Carlos E.
,
Macaya, Alfons
,
Kullmann, Dimitri M.
,
Rothman, James E.
,
Krishnakumar, Shyam S.
,
Houlden, Henry
Published in
American journal of human genetics
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Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination
by
Efthymiou, Stephanie
,
Salpietro, Vincenzo
,
Malintan, Nancy
,
Poncelet, Mallory
,
Kriouile, Yamna
,
Fortuna, Sara
,
De Zorzi, Rita
,
Payne, Katelyn
,
Henderson, Lindsay B
,
Cortese, Andrea
,
Maddirevula, Sateesh
,
Alhashmi, Nadia
,
Wiethoff, Sarah
,
Ryten, Mina
,
Botia, Juan A
,
Provitera, Vincenzo
,
Schuelke, Markus
,
Vandrovcova, Jana
,
Walsh, Laurence
,
Torti, Erin
,
Iodice, Valeria
,
Najafi, Maryam
,
Karimiani, Ehsan Ghayoor
,
Maroofian, Reza
,
Siquier-Pernet, Karine
,
Boddaert, Nathalie
,
De Lonlay, Pascale
,
Cantagrel, Vincent
,
Aguennouz, Mhammed
,
El Khorassani, Mohamed
,
Schmidts, Miriam
,
Alkuraya, Fowzan S
,
Edvardson, Simon
,
Nolano, Maria
,
Devaux, Jérôme
,
Houlden, Henry
Published in
Brain (London, England : 1878)
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Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up
by
Belcastro, Vincenzo
,
Casellato, Susanna
,
Striano, Pasquale
,
Capovilla, Giuseppe
,
Savasta, Salvatore
,
Foiadelli, Thomas
,
Sofia, Vito
,
Giuliano, Loretta
,
Riva, Antonella
,
Elia, Maurizio
,
Cesaroni, Elisabetta
,
Bonaventura, Carlo Di
,
Giallonardo, Teresa
,
Striano, Salvatore
,
Gambardella, Antonio
,
Ferlazzo, Edoardo
,
Verrotti, Alberto
Published in
Seizure (London, England)
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The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic Outcome
by
Veneruso, Marco
,
Fiorillo, Chiara
,
Broda, Paolo
,
Baratto, Serena
,
Traverso, Monica
,
Donati, Alice
,
Savasta, Salvatore
,
Falsaperla, Raffaele
,
Mancardi, Maria Margherita
,
Pedemonte, Marina
,
Panicucci, Chiara
,
Piatelli, Gianluca
,
Pacetti, Mattia
,
Moscatelli, Andrea
,
Ramenghi, Luca Antonio
,
Nobili, Lino
,
Minetti, Carlo
,
Bruno, Claudio
Published in
Frontiers in neurology
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Epilepsy Course and Developmental Trajectories in STXBP1-DEE
by
Balagura, Ganna
,
Xian, Julie
,
Riva, Antonella
,
Marchese, Francesca
,
Ben Zeev, Bruria
,
Rios, Loreto
,
Sirsi, Deepa
,
Accorsi, Patrizia
,
Amadori, Elisabetta
,
Astrea, Guja
,
Baldassari, Simona
,
Beccaria, Francesca
,
Boni, Antonella
,
Budetta, Mauro
,
Cantalupo, Gaetano
,
Capovilla, Giuseppe
,
Cesaroni, Elisabetta
,
Chiesa, Valentina
,
Coppola, Antonietta
,
Dilena, Robertino
,
Faggioli, Raffaella
,
Ferrari, Annarita
,
Fiorini, Elena
,
Madia, Francesca
,
Gennaro, Elena
,
Giacomini, Thea
,
Giordano, Lucio
,
Iacomino, Michele
,
Lattanzi, Simona
,
Marini, Carla
,
Mancardi, Maria Margherita
,
Mastrangelo, Massimo
,
Messana, Tullio
,
Minetti, Carlo
,
Nobili, Lino
,
Papa, Amanda
,
Parmeggiani, Antonia
,
Pisano, Tiziana
,
Russo, Angelo
,
Salpietro, Vincenzo
,
Savasta, Salvatore
,
Scala, Marcello
,
Accogli, Andrea
,
Scelsa, Barbara
,
Scudieri, Paolo
,
Spalice, Alberto
,
Specchio, Nicola
,
Trivisano, Marina
,
Tzadok, Michal
,
Valeriani, Massimiliano
,
Vari, Maria Stella
,
Verrotti, Alberto
,
Vigevano, Federico
,
Vignoli, Aglaia
,
Toonen, Ruud
,
Zara, Federico
,
Helbig, Ingo
,
Striano, Pasquale
Published in
Neurology. Genetics
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Subependymal Periventricular Heterotopias in a Patient With Ehlers-Danlos Syndrome: A New Case
by
Savasta, Salvatore
,
Crispino, Mario
,
Valli, Maurizia
,
Calligaro, Alberto
,
Zambelloni, Cesare
,
Poggiani, Carlo
Published in
Journal of child neurology
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Mitochondrial DNA Deletion in a Child With Mitochondrial Encephalomyopathy, Growth Hormone Deficiency, and Hypoparathyroidism
by
Cassandrini, Denise
,
Savasta, Salvatore
,
Bozzola, Mauro
,
Tessa, Alessandra
,
Pedemonte, Marina
,
Assereto, Stefania
,
Stringara, Silvia
,
Minetti, Carlo
,
Santorelli, Filippo M.
,
Bruno, Claudio
Published in
Journal of child neurology
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