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Plos One|January 4, 2013
Cellular redox imbalance and changes of protein S-glutathionylation patterns are associated with senescence induced by oncogenic H-rasTatiana Armeni, Luisa Ercolani, Lorena Urbanelli, et al.Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 19, 2007
In vitro study of biofunctional indicators after exposure to asbestos-like fluoro-edenite fibresA Pugnaloni, G Lucarini, F GiantomassI, et al.Haematologica|January 1, 1994
Platelet abnormalities in idiopathic myelofibrosis: functional, biochemical and immunomorphological correlationsP Leoni, S Rupoli, G Lai, et al.Experimental Dermatology|October 27, 2004
Local rh-VEGF administration enhances skin flap survival more than other types of rh-VEGF administration: a clinical, morphological and immunohistochemical studyAlessandro Scalise, Maria Giovanna Tucci, Guendalina Lucarini, et al.Pediatric Research|January 20, 2024
Assessment of hemodynamic dysfunction in septic newborns by functional echocardiography: a systematic reviewFlaminia Pugnaloni, Domenico Umberto De Rose, Florian Kipfmueller, et al.Biochemistry and Molecular Biology International|June 1, 1994
Lack of major mitochondrial bioenergetic changes in cultured skin fibroblasts from aged individualsR Solmi, F Pallotti, M Rugolo, et al.Medicina (Kaunas, Lithuania)|March 20, 2020
Impact of Elderly Masticatory Performance on Nutritional Status: An Observational StudyLuca Aquilanti, Sonila Alia, Sofia Pugnaloni, et al.Viruses|April 23, 2022
Multisystem Inflammatory Syndrome in Neonates Born to Mothers with SARS-CoV-2 Infection (MIS-N) and in Neonates and Infants Younger Than 6 Months with Acquired COVID-19 (MIS-C): A Systematic ReviewDomenico Umberto De Rose, Flaminia Pugnaloni, Monica Calì, et al.Physical Review. E|October 24, 2019
Dynamics of a grain-scale intruder in a two-dimensional granular medium with and without basal frictionRyan Kozlowski, C Manuel Carlevaro, Karen E Daniels, et al.Italian Journal of Pediatrics|September 18, 2024
Neonatal Marfan syndrome: a case report of a novel fibrillin 1 mutation, with genotype-phenotype correlation and brief review of the literatureFlaminia Pugnaloni, Domenico Umberto De Rose, Maria Cristina Digilio, et al.Pageof 19