Nafissi, Shahriar
Nafissi, Shahriar
Professor of Neurology, Neuromuscular Research Center, Tehran University of medical sciences
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KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2
JB Rivière, S Ramalingam, V Lavastre, M Shekarabi, S Holbert, ...
The American Journal of Human Genetics, 2011
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect
J Senderek, JS Muller, M Dusl, TM Strom, V Guergueltcheva, I Diepolder, ...
The American Journal of Human Genetics 88 (2), 162-172, 2011
Quality of life of people with epilepsy in Iran, the Gulf, and Near East
GA Baker, A Jacoby, J Gorry, J Doughty, V Ellina, SIGN Group
Epilepsia 46 (1), 132-140, 2005
COVID-19-associated risks and effects in myasthenia gravis (CARE-MG)
S Muppidi, JT Guptill, S Jacob, Y Li, ME Farrugia, AC Guidon, JO Tavee, ...
The Lancet Neurology 19 (12), 970-971, 2020
Safety and efficacy of nanocurcumin as add-on therapy to riluzole in patients with amyotrophic lateral sclerosis: a pilot randomized clinical trial
M Ahmadi, E Agah, S Nafissi, MR Jaafari, MH Harirchian, P Sarraf, ...
Neurotherapeutics 15 (2), 430-438, 2018
International clinimetric evaluation of the MG‐QOL15, resulting in slight revision and subsequent validation of the MG‐QOL15r
TM Burns, R Sadjadi, K Utsugisawa, KG Gwathmey, A Joshi, S Jones, ...
Muscle & nerve 54 (6), 1015-1022, 2016
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations
V Guergueltcheva, JS Müller, M Dusl, J Senderek, A Oldfors, C Lindbergh, ...
Journal of neurology 259 (5), 838-850, 2012
Mitochondrial complex I deficiency and ATP/ADP ratio in lymphocytes of amyotrophic lateral sclerosis patients
P Ghiasi, S Hosseinkhani, A Noori, S Nafissi, K Khajeh
Neurological research 34 (3), 297-303, 2012
Effect of vitamin A supplementation on fatigue and depression in multiple sclerosis patients: a double-blind placebo-controlled clinical trial
S Bitarafan, A Saboor-Yaraghi, MA Sahraian, D Soltani, S Nafissi, ...
Iranian Journal of Allergy, Asthma and Immunology 15 (1), 13-19, 2016
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations
I Wargon, P Richard, T Kuntzer, D Sternberg, S Nafissi, K Gaudon, ...
Neuromuscular Disorders 22 (4), 318-324, 2012
Impact of depression and disability on quality of life in Iranian patients with multiple sclerosis
P Ayatollahi, S Nafissi, MR Eshraghian, H Kaviani, A Tarazi
Multiple Sclerosis 13 (2), 275-277, 2007
Complex I and ATP content deficiency in lymphocytes from Friedreich's ataxia
MM Heidari, M Houshmand, S Hosseinkhani, S Nafissi, M Khatami
Canadian journal of neurological sciences 36 (1), 26-31, 2009
Wilson’s disease: a great masquerader
A Soltanzadeh, P Soltanzadeh, S Nafissi, A Ghorbani, H Sikaroodi, J Lotfi
European Neurology 57 (2), 80-85, 2007
Dietary intake of nutrients and its correlation with fatigue in multiple sclerosis patients
S Bitarafan, MH Harirchian, S Nafissi, MA Sahraian, M Togha, F Siassi, ...
Iranian journal of neurology 13 (1), 28, 2014
Comparison of electrophysiological findings in axonal and demyelinating Guillain-Barre syndrome
S Yadegari, S Nafissi, N Kazemi
Iranian Journal of Neurology 13 (3), 138-143, 2014
Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain
E Jaberi, M Rohani, GA Shahidi, S Nafissi, E Arefian, M Soleimani, ...
Neurobiology of Aging 38, 216. e11-216. e18, 2016
Impact of Vitamin A Supplementation on Disease Progression in Patients with Multiple Sclerosis.
S Bitarafan, A Saboor-Yaraghi, MA Sahraian, S Nafissi, M Togha, ...
Archives of Iranian medicine 18 (7), 435-440, 2015
Silibinin inhibits invasive properties of human glioblastoma U87MG cells through suppression of cathepsin B and nuclear factor kappa B-mediated induction of matrix …
M Momeny, M Malehmir, M Zakidizaji, R Ghasemi, H Ghadimi, ...
Anti-cancer drugs 21 (3), 252, 2010
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population
Z Fattahi, Z Kalhor, M Fadaee, R Vazehan, E Parsimehr, A Abolhassani, ...
Clinical genetics 91 (3), 386-402, 2017
Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients
A Alavi, S Nafissi, M Rohani, B Zamani, B Sedighi, H Shamshiri, JB Fan, ...
Neurobiology of aging 34 (5), 1516. e1-1516. e8, 2013
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