Nafissi, Shahriar

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Farzad FatehiProfessor of Neurology, Shariati Hospital, Tehran university of medical sciencesAdresse e-mail validée de tums.ac.ir
elahe elahiUniversity of TehranAdresse e-mail validée de ut.ac.ir
Ali Asghar OkhovatTehran University of Medical SciencesAdresse e-mail validée de sina.tums.ac.ir
Mohammad Hossein HarirchianTehran University of Medical Sciences, Iranian Center of Neurological ResearchAdresse e-mail validée de sina.tums.ac.ir
mohammad rohaniProfessor of neurology, Iran University of Medical SciencesAdresse e-mail validée de iums.ac.ir
Kimia KahriziProfessor of Medicine, Thessaly UniversityAdresse e-mail validée de uth.gr
Hossein NajmabadiGenetics Research Center, University of Social Welfare and Rehabilitation SciencesAdresse e-mail validée de uswr.ac.ir
Mansoureh ToghaTehran University of Medical SciencesAdresse e-mail validée de tums.ac.ir
Nahid Beladi-MoghadamShahid Beheshti University of Medical SciencesAdresse e-mail validée de sbmu.ac.ir
Marzieh KhaniNational Institute of HealthAdresse e-mail validée de nih.gov
Mohammad Ali SahraianProfessor of Neurology, MS Research Center, Neuroscience Institute, Tehran University of MedicalAdresse e-mail validée de sina.tums.ac.ir
Massoud HoushmandProfessor in Genetic Diagnostic department; NIGEBAdresse e-mail validée de nigeb.ac.ir
bentolhoda ziaadiniKerman universoty of medical sciences,department of neurologyAdresse e-mail validée de kmu.ac.ir
babak zamaniiran university of medical sciencesAdresse e-mail validée de iums.ac.ir
Bahram Haghi AshtianiAssociate Professor of Neurology School of Medicine Iran University of Medical SciencesAdresse e-mail validée de iums.ac.ir
Farnaz SinaeiTehran University of Medical SciencesAdresse e-mail validée de sina.tums.ac.ir
Samira YadegariAssociate Professor of Neurology,Department of Neuro-ophthalmology, Farabi Eye Hospital, TehranAdresse e-mail validée de sina.tums.ac.ir
seyed hassan tonekaboniprofessor of pediatrics in shahid beheshti medical university ( SBMU)Adresse e-mail validée de sbmu.ac.ir
Narges KarimiAssociate Professor of Neurology, Neuromuscular fellowship, Immunogenetics Research CenterAdresse e-mail validée de mazums.ac.ir
Saman HosseinkhaniTarbiat Modares UniversityAdresse e-mail validée de modares.ac.ir

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Nafissi, Shahriar

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

Adresse e-mail validée de sina.tums.ac.ir - Page d'accueil

Neurology Neuromuscular neuroscience genetics


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
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	213	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	192	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	179	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	128	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	122	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	117	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	99	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	91	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	82	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	78	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	70	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	68	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
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	61	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	60	2016
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	60	2014
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	57	2018
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
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	52	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	51	2018

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