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The American Journal of Cardiology|December 8, 2009
Histopathology of clinical coronary restenosis in drug-eluting versus bare metal stentsAlaide Chieffo, Chiara Foglieni, Rota Laura Nodari, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 8, 2022
Scn1b expression in the adult mouse heart modulates Na+ influx in myocytes and reveals a mechanistic link between Na+ entry and diastolic functionDaniel O Cervantes, Emanuele Pizzo, Harshada Ketkar, et al.
Plos One|April 5, 2024
Impact of improved dead time correction on the quantification accuracy of a dedicated BrainPET scannerAhlam Said Mohamad Issa, Jürgen Scheins, Lutz Tellmann, et al.
Vaccines|August 29, 2024
Building Quality Control for Molecular Assays in the Global Measles and Rubella Laboratory NetworkBettina Bankamp, Raydel Anderson, Lijuan Hao, et al.
Evolution & Development|November 1, 2006
Mitogenomics and phylogenomics reveal priapulid worms as extant models of the ancestral EcdysozoanBonnie L Webster, Richard R Copley, Ronald A Jenner, et al.
The Journal of Gene Medicine|September 8, 2004
Marked inhibition of retinal neovascularization in rats following soluble-flt-1 gene transferRossella Rota, Teresa Riccioni, Marco Zaccarini, et al.
Stem Cell Research & Therapy|February 12, 2026
NAMPT overexpression enhances the regenerative potential of mesenchymal stromal cell-derived extracellular vesicles in experimental AKISimona Buelli, Michelle Prioli Miranda Soares, Anna Pezzotta, et al.
Epilepsia Open|November 10, 2025
A prospective randomized crossover trial investigating melatonin versus sleep deprivation for sleep induction in nap electroencephalographyValentina De Giorgis, Costanza Varesio, Massimiliano Celario, et al.
Nuclear Medicine Communications|November 19, 2013
Relationship of regional cerebral blood flow and kinetic behaviour of O-(2-(18)F-fluoroethyl)-L-tyrosine uptake in cerebral gliomasKe Zhang, Karl-Josef Langen, Irene Neuner, et al.
European Journal of Human Genetics : EJHG|March 31, 2016
ASAH1 variant causing a mild SMA phenotype with no myoclonic epilepsy: a clinical, biochemical and molecular studyMassimiliano Filosto, Massimo Aureli, Barbara Castellotti, et al.
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