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Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2010
Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndromeSimona Giovannini, Daniele Frattini, Angela Scarano, et al.
American Journal of Human Genetics|February 10, 2009
A missense mutation in CASK causes FG syndrome in an Italian familyGiulio Piluso, Francesca D'Amico, Valentina Saccone, et al.
Eye (London, England)|July 9, 2025
Quantifying macular atrophy in neovascular AMD using en face structural OCT imagingChiara Olivieri, Tommaso Tibaldi, Alessandro Berni, et al.
Molecules (Basel, Switzerland)|May 11, 2024
Absorption and Fluorescence Emission Investigations on Supramolecular Assemblies of Tetrakis-(4-sulfonatophenyl)porphyrin and Graphene Quantum DotsMariachiara Sarà, Salvatore Vincenzo Giofrè, Salvatore Abate, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Treatment with valproic acid ameliorates ADHD symptoms in fragile X syndrome boysMariagiulia Torrioli, Silvia Vernacotola, Chiara Setini, et al.
American Journal of Medical Genetics. Part A|November 12, 2005
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndromeFernanda Sarquis Jehee, Carla Rosenberg, Ana Cristina Krepischi-Santos, et al.
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.
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