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Neurobiology of Aging|August 18, 2004
MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levelsChiara Fenoglio, Daniela Galimberti, Carlo Lovati, et al.
Journal of Neurology|June 26, 2008
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegiaRoberta Virgilio, Dario Ronchi, Georgios M Hadjigeorgiou, et al.
Neurobiology of Aging|September 25, 2007
Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?Serena Ghezzi, Roberto Del Bo, Marina Scarlato, et al.
Frontiers in Neurology|February 15, 2021
Case Report: Efficacy of Rituximab in a Patient With Familial Mediterranean Fever and Multiple SclerosisMattia Pozzato, Emanuele Micaglio, Chiara Starvaggi Cucuzza, et al.
Frontiers in Neurology|October 31, 2018
Stormorken Syndrome Caused by a p.R304W STIM1 Mutation: The First Italian Patient and a Review of the LiteratureOscar Borsani, Daniela Piga, Stefania Costa, et al.
Human Molecular Genetics|December 13, 2005
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
The Journal of Cell Biology|July 30, 2003
Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy modelYvan Torrente, Geoffrey Camirand, Federica Pisati, et al.
BMC Neurology|August 28, 2020
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENGDavide Villa, Claudia Cinnante, Gloria Valcamonica, et al.
Cellular and Molecular Life Sciences : CMLS|December 24, 2011
Variants in SNAP25 are targets of natural selection and influence verbal performances in womenRachele Cagliani, Stefania Riva, Cecilia Marino, et al.
Human Molecular Genetics|August 11, 2016
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neuronsFederica Rizzo, Dario Ronchi, Sabrina Salani, et al.
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