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Frontiers in Systems Neuroscience|August 1, 2020
Experimental and Computational Study on Motor Control and Recovery After Stroke: Toward a Constructive Loop Between Experimental and Virtual Embodied NeuroscienceAnna Letizia Allegra Mascaro, Egidio Falotico, Spase Petkoski, et al.
European Heart Journal|November 22, 2020
Brugada syndrome genetics is associated with phenotype severityGiuseppe Ciconte, Michelle M Monasky, Vincenzo Santinelli, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 3, 2020
Prediction of pre-eclampsia in twin pregnancy by maternal factors and biomarkers at 11-13 weeks' gestation: data from EVENTS trialZ Benkő, A Wright, A Rehal, et al.
Forensic Science International. Genetics|December 3, 2014
Development of an Italian RM Y-STR haplotype database: Results of the 2013 GEFI collaborative exerciseC Robino, A Ralf, S Pasino, et al.
Journal of the American Heart Association|April 7, 2026
Red Flags for Differentiating Desmosomal "Hot-Phase" Cardiomyopathy From Acute MyocarditisGiovanni Peretto, Nicolas Piriou, Alessio Gasperetti, et al.
La Clinica Terapeutica|July 9, 2015
Immediately loaded dental implants bioactivated with platelet-rich plasma (PRP) placed in maxillary and mandibular regionF Inchingolo, A Ballini, R Cagiano, et al.
The New England Journal of Medicine|March 1, 2002
Hematologic and cytogenetic responses to imatinib mesylate in chronic myelogenous leukemiaHagop Kantarjian, Charles Sawyers, Andreas Hochhaus, et al.
American Journal of Human Genetics|February 7, 2015
COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiencyGloria Brea-Calvo, Tobias B Haack, Daniela Karall, et al.
Turkish Thoracic Journal|July 21, 2020
Continuous Positive Airway Pressure (CPAP) in Non-Apneic Asthma: A Clinical Review of Current EvidenceHabib Mohammad Reazaul Karim, Antonio M Esquinas, Sally Ziatabar, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|February 19, 2013
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter studyNicoletta Resta, Daniela Pierannunzio, Gennaro Mariano Lenato, et al.
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