The Sac1 Domain of SYNJ1 Identified Mutated in a Family with Early‐Onset Progressive Parkinsonism with Generalized Seizures CE Krebs, S Karkheiran, JC Powell, M Cao, V Makarov, H Darvish, ... Human mutation 34 (9), 1200-1207, 2013 | 388 | 2013 |
Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays S Shojaee, F Sina, SS Banihosseini, MH Kazemi, R Kalhor, GA Shahidi, ... The American Journal of Human Genetics 82 (6), 1375-1384, 2008 | 331 | 2008 |
Defining spasticity: a new approach considering current movement disorders terminology and botulinum toxin therapy D Dressler, R Bhidayasiri, S Bohlega, P Chana, HF Chien, TM Chung, ... Journal of neurology 265, 856-862, 2018 | 100 | 2018 |
A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study A Münchau, EM Valente, GA Shahidi, LH Eunson, MG Hanna, NP Quinn, ... Journal of Neurology, Neurosurgery & Psychiatry 68 (5), 609-614, 2000 | 99 | 2000 |
A clinical and molecular genetic study of 50 families with autosomal recessive parkinsonism revealed known and novel gene mutations S Taghavi, R Chaouni, A Tafakhori, LJ Azcona, SG Firouzabadi, ... Molecular neurobiology 55, 3477-3489, 2018 | 88 | 2018 |
Motor, psychiatric and fatigue features associated with nutritional status and its effects on quality of life in Parkinson’s disease patients SM Fereshtehnejad, L Ghazi, M Shafieesabet, GA Shahidi, A Delbari, ... PLoS One 9 (3), e91153, 2014 | 76 | 2014 |
Retinal nerve changes in patients with tremor dominant and akinetic rigid Parkinson’s disease M Rohani, AS Langroodi, S Ghourchian, KG Falavarjani, R SoUdi, ... Neurological Sciences 34, 689-693, 2013 | 74 | 2013 |
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticity D Dressler, MC Altavista, E Altenmueller, R Bhidayasiri, S Bohlega, ... Journal of Neural Transmission 128, 321-335, 2021 | 70 | 2021 |
Restless legs syndrome in patients with Parkinson's disease: a comparative study on prevalence, clinical characteristics, quality of life and nutritional status SM Fereshtehnejad, M Shafieesabet, GA Shahidi, A Delbari, J Lökk Acta Neurologica Scandinavica 131 (4), 211-218, 2015 | 66 | 2015 |
Relationship between voice and motor disabilities of Parkinson's disease F Majdinasab, S Karkheiran, M Soltani, N Moradi, G Shahidi Journal of Voice 30 (6), 768. e17-768. e22, 2016 | 64 | 2016 |
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 |
Mini Nutritional Assessment (MNA) is rather a reliable and valid instrument to assess nutritional status in Iranian healthy adults and elderly with a chronic disease L Ghazi, SM Fereshtehnejad, S Abbasi Fard, M Sadeghi, GA Shahidi, ... Ecology of food and nutrition 54 (4), 342-357, 2015 | 56 | 2015 |
Botulinum toxin therapy for treatment of spasticity in multiple sclerosis: review and recommendations of the IAB-Interdisciplinary Working Group for Movement Disorders task force D Dressler, R Bhidayasiri, S Bohlega, A Chahidi, TM Chung, M Ebke, ... Journal of neurology 264, 112-120, 2017 | 53 | 2017 |
PLA2G6-associated dystonia–parkinsonism: Case report and literature review S Karkheiran, GA Shahidi, RH Walker, C Paisán-Ruiz Tremor and Other Hyperkinetic Movements 5, 2015 | 50 | 2015 |
Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients H Darvish, A Movafagh, MD Omrani, SG Firouzabadi, E Azargashb, ... Neuroscience letters 551, 75-78, 2013 | 49 | 2013 |
Prevalence of malnutrition in patients with Parkinson's disease: a comparative study with healthy controls using Mini Nutritional Assessment (MNA) questionnaire SM Fereshtehnejad, L Ghazi, M Sadeghi, D Khaefpanah, GA Shahidi, ... Journal of Parkinson's disease 4 (3), 473-481, 2014 | 48 | 2014 |
Reliability and validity of the Persian version of the fatigue severity scale in idiopathic Parkinson’s disease patients SM Fereshtehnejad, H Hadizadeh, F Farhadi, GA Shahidi, A Delbari, ... Parkinson’s Disease 2013 (1), 935429, 2013 | 48 | 2013 |
Heterogeneous determinants of quality of life in different phenotypes of Parkinson’s disease SM Fereshtehnejad, M Shafieesabet, F Farhadi, H Hadizadeh, ... PloS one 10 (9), e0137081, 2015 | 46 | 2015 |
Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients A Alavi, S Nafissi, M Rohani, G Shahidi, B Zamani, H Shamshiri, I Safari, ... Neurobiology of aging 35 (1), 267. e1-267. e7, 2014 | 44 | 2014 |
Mutation in ADORA1 identified as likely cause of early‐onset parkinsonism and cognitive dysfunction E Jaberi, M Rohani, GA Shahidi, S Nafissi, E Arefian, M Soleimani, ... Movement Disorders 31 (7), 1004-1011, 2016 | 42 | 2016 |