Nafissi, Shahriar

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Farzad FatehiProfessor of Neurology, Shariati Hospital, Tehran university of medical sciencesVerified email at tums.ac.ir
elahe elahiUniversity of TehranVerified email at ut.ac.ir
Ali Asghar OkhovatTehran University of Medical SciencesVerified email at sina.tums.ac.ir
Mohammad Hossein HarirchianTehran University of Medical Sciences, Iranian Center of Neurological ResearchVerified email at sina.tums.ac.ir
mohammad rohaniProfessor of neurology, Iran University of Medical SciencesVerified email at iums.ac.ir
Kimia KahriziProfessor of Medicine, Thessaly UniversityVerified email at uth.gr
Mansoureh ToghaTehran University of Medical SciencesVerified email at tums.ac.ir
Hossein NajmabadiGenetics Research Center, University of Social Welfare and Rehabilitation SciencesVerified email at uswr.ac.ir
Nahid Beladi-MoghadamShahid Beheshti University of Medical SciencesVerified email at sbmu.ac.ir
Marzieh KhaniNational Institute of HealthVerified email at nih.gov
Massoud HoushmandProfessor in Genetic Diagnostic department; NIGEBVerified email at nigeb.ac.ir
babak zamaniiran university of medical sciencesVerified email at iums.ac.ir
Bahram Haghi AshtianiAssociate Professor of Neurology School of Medicine Iran University of Medical SciencesVerified email at iums.ac.ir
Farnaz SinaeiTehran University of Medical SciencesVerified email at sina.tums.ac.ir
Samira YadegariAssociate Professor of Neurology,Department of Neuro-ophthalmology, Farabi Eye Hospital, TehranVerified email at sina.tums.ac.ir
bentolhoda ziaadiniKerman universoty of medical sciences,department of neurologyVerified email at kmu.ac.ir
seyed hassan tonekaboniprofessor of pediatrics in shahid beheshti medical university ( SBMU)Verified email at sbmu.ac.ir
Sama Bitarafan, MD, PhD, RDResearch consultant at Fraser Health Authority, RD(t), BC, CanadaVerified email at Fraserhealth.ca
Saman HosseinkhaniTarbiat Modares UniversityVerified email at modares.ac.ir
Volker StraubNewcastle UniversityVerified email at ncl.ac.uk

Nafissi, Shahriar

Professor of Neurology, Neuromuscular Research Center, Tehran University of medical sciences

Verified email at sina.tums.ac.ir - Homepage

Neurology Neuromuscular neuroscience genetics


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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	205	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	186	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	175	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	122	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	115	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	110	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	96	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	90	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	81	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	76	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	68	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	67	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	65	2007
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	59	2014
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	57	2015
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	57	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	56	2016
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	50	2017
Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained … K Johnson, M Bertoli, L Phillips, A Töpf, P Van den Bergh, J Vissing, ... Skeletal muscle 8 (1), 23, 2018	49	2018
Phenotypic stratification and genotype–phenotype correlation in a heterogeneous, international cohort of GNE myopathy patients: First report from the GNE myopathy Disease … O Pogoryelova, P Cammish, H Mansbach, Z Argov, I Nishino, A Skrinar, ... Neuromuscular Disorders 28 (2), 158-168, 2018	49	2018

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