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European Journal of Human Genetics : EJHG|October 16, 2003
Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophyCatia Andreassi, Carla Angelozzi, Francesco D Tiziano, et al.International Journal of Pharmaceutics|April 19, 2025
A smart β-Cyclodextrin-Aza[5]Helicene system for enhanced gemcitabine delivery and tracking in cancer cellsConsuelo Celesti, Andrea Mele, Claudia Espro, et al.Current Oncology (Toronto, Ont.)|April 25, 2025
A Rare Malignant Case of a Primary Pseudomyogenic Haemangioendothelioma of the BoneAnnabella Di Mauro, Salvatore Tafuto, Lucia Cannella, et al.European Child & Adolescent Psychiatry|January 25, 2021
Factors associated with the transition of adolescent inpatients from an intensive residential ward to adult mental health servicesGiancarlo Pontoni, Elena Di Pietro, Tommaso Neri, et al.Eye (London, England)|January 9, 2025
Deep learning model for automatic detection of different types of microaneurysms in diabetic retinopathyGiovanni Neri, Sohum Sharma, Beatrice Ghezzo, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 10, 2012
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutationAmelia Conte, Serena Lattante, Marco Luigetti, et al.American Journal of Medical Genetics. Part A|September 15, 2005
Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndromeGermán Rodríguez-Criado, Luis Magano, Mabel Segovia, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 25, 2026
Review of emerging imaging findings to reveal a broader spectrum of lesions in AMDEnrico Borrelli, Giovanni Neri, Alessandro Berni, et al.Journal of Crohn'S & Colitis|December 29, 2025
Inflammatory Bowel Disease is associated with increased intestinal extrachromosomal circular DNA: an emerging biomarker for IBD type and activityValentina Petito, Daniela Gerovska, Antonia Piazzesi, et al.Journal of Neurology|December 25, 2012
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansionsMassimo Santoro, Marcella Masciullo, Roberta Pietrobono, et al.Pageof 30