Showing results (601-610 of 697) with videos related to
Sort By:
Pageof 70
Leukemia|May 19, 2009
Analysis of the host pharmacogenetic background for prediction of outcome and toxicity in diffuse large B-cell lymphoma treated with R-CHOP21D Rossi, S Rasi, S Franceschetti, et al.Journal of Clinical Medicine|October 14, 2023
Results of the Italian RESILIEN-T Pilot Study: A Mobile Health Tool to Support Older People with Mild Cognitive ImpairmentRoberta Bevilacqua, Elisa Felici, Giacomo Cucchieri, et al.Neurorehabilitation and Neural Repair|September 12, 2015
Is Period3 Genotype Associated With Sleep and Recovery in Patients With Disorders of Consciousness?Gloria Bedini, Anna Bersano, Davide Rossi Sebastiano, et al.Epilepsia Open|January 31, 2023
Progressive myoclonus epilepsies due to SEMA6B mutations. New variants and appraisal of published phenotypesBarbara Castellotti, Laura Canafoglia, Elena Freri, et al.Substance Use & Misuse|February 27, 2020
Prevalence, Correlates and Outcomes of Smoking in Pregnant Women with HIV: A National Observational Study in ItalyMarco Floridia, Marina Ravizza, Giulia Masuelli, et al.European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|January 9, 2022
Minimal prevalence of HPV vaccination and common occurrence of high-risk HPV types in pregnant women with HIV: data from a national study in ItalyMarco Floridia, Giulia Masuelli, Beatrice Tassis, et al.Journal of Neurology|March 22, 2019
Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypesBarbara Castellotti, Francesca Ragona, Elena Freri, et al.Hematological Oncology|August 10, 2006
Analysis of immunoglobulin heavy and light chain variable genes in post-transplant lymphoproliferative disordersDaniela Capello, Michaela Cerri, Giuliana Muti, et al.Proceedings of the National Academy of Sciences of the United States of America|December 6, 2005
Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizuresMassimo Mantegazza, Antonio Gambardella, Raffaella Rusconi, et al.Expert Review of Neurotherapeutics|January 17, 2020
Advances in genetic testing and optimization of clinical management in children and adults with epilepsyMarcello Scala, Amedeo Bianchi, Francesca Bisulli, et al.Pageof 70