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Bioorganic & Medicinal Chemistry Letters|October 22, 2008
2-Trifluoroacetylthiophene oxadiazoles as potent and selective class II human histone deacetylase inhibitorsEster Muraglia, Sergio Altamura, Danila Branca, et al.
Scientific Reports|July 19, 2018
P31-43, an undigested gliadin peptide, mimics and enhances the innate immune response to viruses and interferes with endocytic trafficking: a role in celiac diseaseMerlin Nanayakkara, Giuliana Lania, Mariantonia Maglio, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|May 1, 2023
Acute heart failure: differential diagnosis and treatmentMarco Marini, Roberto Manfredi, Ilaria Battistoni, et al.
The Prostate|March 21, 2012
Serum sarcosine increases the accuracy of prostate cancer detection in patients with total serum PSA less than 4.0 ng/mlGiuseppe Lucarelli, Margherita Fanelli, Angela Maria Vittoria Larocca, et al.
American Journal of Ophthalmology|September 23, 2025
Macular Edema Resistance in Retinal Vein Occlusion and the Protective Role of PAMM SubtypesMaria Vittoria Cicinelli, Enrico Maria Pepe, Beatrice Tombolini, et al.
International Journal of Molecular Sciences|August 14, 2025
Proteomic Insights into Bacterial Responses to Antibiotics: A Narrative ReviewSara Elsa Aita, Maria Vittoria Ristori, Antonio Cristiano, et al.
Nanoscale|August 4, 2025
Halloysite nanotubes as a vector for hydrophobic perfluorinated porphyrin-based photosensitizers for singlet oxygen generationHady Hamza, Veronica Schifano, Giorgia Colciago, et al.
Optics Express|April 24, 2013
Electronic temperatures of terahertz quantum cascade active regions with phonon scattering assisted injection and extraction schemePietro Patimisco, Gaetano Scamarcio, Maria Vittoria Santacroce, et al.
Leukemia Research|November 3, 2017
High prognostic value of pre-allogeneic stem cell transplantation minimal residual disease detection by WT1 gene expression in AML transplanted in cytologic complete remissionAnna Candoni, Federico De Marchi, Maria Elena Zannier, et al.
Orphanet Journal of Rare Diseases|October 9, 2016
Viable phenotype of ILNEB syndrome without nephrotic impairment in siblings heterozygous for unreported integrin alpha3 mutationsElisa Adele Colombo, Luigina Spaccini, Ludovica Volpi, et al.
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