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Journal of Neuropathology and Experimental Neurology|September 8, 2006
NMDA receptor composition differs among anatomically diverse malformations of cortical developmentAdele Finardi, Fabrizio Gardoni, Stefania Bassanini, et al.Nature Genetics|March 9, 2010
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 24, 2022
IDEAL study: A real-world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX-FP) in patients with haemophilia B in ItalyAnnarita Tagliaferri, Angelo Claudio Molinari, Flora Peyvandi, et al.Pageof 2