gholamali shahidi
gholamali shahidi
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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
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
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
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
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 (5), 689-693, 2013
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 (4), 3477-3489, 2018
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
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
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
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
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
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 (4), 856-862, 2018
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
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
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, 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
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
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
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 (1), 112-120, 2017
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
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