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Human Mutation|November 4, 2004
Transfer of a mitochondrial DNA fragment to MCOLN1 causes an inherited case of mucolipidosis IVEhud Goldin, Stefanie Stahl, Adele M Cooney, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 12, 2017
Low frequency of Fabry disease in patients with common heart diseaseRaphael Schiffmann, Caren Swift, Nathan McNeill, et al.Molecular Genetics and Metabolism|August 19, 2008
Globotriaosylceramide induces oxidative stress and up-regulates cell adhesion molecule expression in Fabry disease endothelial cellsJin-Song Shen, Xing-Li Meng, David F Moore, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 31, 2019
Consistent control of disease activity with fingolimod versus IFN β-1a in paediatric-onset multiple sclerosis: further insights from PARADIGMSKumaran Deiva, Peter Huppke, Brenda Banwell, et al.Annals of Neurology|February 29, 2008
Lesion distribution in children with clinically isolated syndromesRezwan Ghassemi, Samson B Antel, Sridar Narayanan, et al.Neurology|August 31, 2016
MRI in the evaluation of pediatric multiple sclerosisBrenda Banwell, Douglas L Arnold, Jan-Mendelt Tillema, et al.Plos One|June 12, 2019
High rates of health care utilization in pediatric multiple sclerosis: A Canadian population-based studyRuth Ann Marrie, Julia O'Mahony, Colleen J Maxwell, et al.Blood Cells, Molecules & Diseases|June 18, 2002
Decreased bone density in splenectomized Gaucher patients receiving enzyme replacement therapyRaphael Schiffmann, Henry Mankin, James M Dambrosia, et al.Neurology(R) Neuroimmunology & Neuroinflammation|May 16, 2019
Pilot study of a ketogenic diet in relapsing-remitting MSJ Nicholas Brenton, Brenda Banwell, A G Christina Bergqvist, et al.Annals of Neurology|February 27, 2024
Epstein-Barr Virus Strongly Associates With Pediatric Multiple Sclerosis, But Not Myelin Oligodendrocyte Glycoprotein-Antibody-Associated DiseaseGiulia Fadda, Carmen Yea, Julia O'Mahony, et al.Pageof 41