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Italian Journal of Pediatrics|October 15, 2023
Use of levosimendan in hemodynamic management of heart failure in two neonates with intracranial arteriovenous shunts: a case seriesFrancesca Landolfo, Paola Giliberti, Domenico Umberto De Rose, et al.Scientific Reports|May 26, 2022
Determinants of variability in signature whistles of the Mediterranean common bottlenose dolphinGabriella La Manna, Nikolina Rako-Gospić, Daniela Silvia Pace, et al.Journal of Cellular and Molecular Medicine|April 3, 2026
Identification of ceRNA Regulatory Networks Driven by the lncRNA NEAT1 in Multiple MyelomaDomenica Ronchetti, Valentina Traini, Ilaria Silvestris, et al.Clinical Chemistry and Laboratory Medicine|April 18, 2025
The accuracy of presepsin in diagnosing neonatal late-onset sepsis in critically ill neonates: a prospective studyCinzia Auriti, Domenico Umberto De Rose, Chiara Maddaloni, et al.The Journal of Investigative Dermatology|November 18, 2006
Pseudoxanthoma elasticum-like phenotype with cutis laxa and multiple coagulation factor deficiency represents a separate genetic entityOlivier M Vanakker, Ludovic Martin, Dealba Gheduzzi, et al.Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|May 6, 2014
Prevalence of HPV infection among clinically healthy Italian males and genotype concordance between stable sexual partnersLaura Lorenzon, Irene Terrenato, Maria Gabriella Donà, et al.Journal of Biomechanics|February 2, 2019
An image-based kinematic model of the tibiotalar and subtalar joints and its application to gait analysis in children with Juvenile Idiopathic ArthritisErica Montefiori, Luca Modenese, Roberto Di Marco, et al.Journal of Cellular and Molecular Medicine|November 28, 2020
Deficit of glucocorticoid-induced leucine zipper amplifies angiotensin-induced cardiomyocyte hypertrophy and diastolic dysfunctionDonato Cappetta, Antonella De Angelis, Sara Flamini, et al.Circulation Research|March 12, 2005
A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 geneSilvia G Priori, Sandeep V Pandit, Ilaria Rivolta, et al.Nature Genetics|June 3, 2000
Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticumO Le Saux, Z Urban, C Tschuch, et al.Pageof 86