Search Results - "Omar, Fadya"

(Un)standardized testing: the diagnostic odyssey of children with rare genetic disorders in Alberta, Canada by Michaels-Igbokwe, Christine, McInnes, Brenda, MacDonald, Karen V., Currie, Gillian R., Omar, Fadya, Shewchuk, Brittany, Bernier, Francois P., Marshall, Deborah A.

“…Purpose We provide a description of the diagnostic odyssey for a cohort of children seeking diagnosis of a rare genetic disorder in terms of the time from…”
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MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease by Kerr, Marina, Hume, Stacey, Omar, Fadya, Koo, Desmond, Barnes, Heather, Khan, Maida, Aman, Suhaib, Wei, Xing-Chang, Alfuhaid, Hanen, McDonald, Roman, McDonald, Liam, Newell, Christopher, Sparkes, Rebecca, Hittel, Dustin, Khan, Aneal

“…Mitochondrial diseases, due to nuclear or mitochondrial genome mutations causing mitochondrial dysfunction, have a wide range of clinical features involving…”
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Integrating Cardiac MRI Imaging and Multidisciplinary Clinical Care is Associated With Improved Outcomes in Patients With Fabry Disease by Perera, Kevin, Kashyap, Niharika, Wang, Kaiming, Omar, Fadya, Prosia, Easter, Thompson, Richard B., Paterson, D. Ian, Fine, Nowell M., White, James A., Khan, Aneal, Oudit, Gavin Y.

“…Given the inherent complexities of Fabry disease (FD) and evolving landscape of cardiovascular clinical management, there is no established ideal clinical care…”
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