Mitra Ansari Dezfouli
Mitra Ansari Dezfouli
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PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation
MA Dezfouli, A Alavi, M Rohani, M Rezvani, T Nekuie, B Klotzle, ...
Movement Disorders 28 (2), 228-231, 2013
Four novel C20orf54 mutations identified in Brown–Vialetto–Van Laere syndrome patients
MA Dezfouli, S Yadegari, S Nafissi, E Elahi
Journal of human genetics 57 (9), 613-617, 2012
Melatonin protective effect against amyloid β-induced neurotoxicity mediated by mitochondrial biogenesis; involvement of hippocampal Sirtuin-1 signaling pathway
MA Dezfouli, M Zahmatkesh, M Farahmandfar, F Khodagholi
Physiology & behavior 204, 65-75, 2019
Common genetic variant in VIT is associated with human brain asymmetry
SH Tadayon, M Vaziri-Pashkam, P Kahali, M Ansari Dezfouli, ...
Frontiers in human neuroscience 10, 236, 2016
Simvastatin attenuates hippocampal MMP-9 expression in the streptozotocin-induced cognitive impairment
S Adeli, M Zahmatkesh, MA Dezfouli
Iranian biomedical journal 23 (4), 262, 2019
Pantothenate kinase 2 mutation with eye-of-the-tiger sign on magnetic resonance imaging in three siblings
MA Dezfouli, E Jaberi, A Alavi, M Rezvani, G Shahidi, E Elahi, M Rohani
Iranian journal of neurology 11 (4), 155, 2012
A Commentary on ‘Four novel C20ORF54 mutations identified in Brown–Vialetto–Van Laere syndrome patients.’
H Houlden
Journal of human genetics 57 (9), 555-555, 2012
Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings
S Yadegari, A Ghorbani, MA Dezfouli, S Nafissi
Iranian journal of neurology 10 (3-4), 54, 2011
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