|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
|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
|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
|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
|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
|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
|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
|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
|The novel mutation p. Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine|
E Jaberi, F Chitsazian, GA Shahidi, M Rohani, F Sina, I Safari, MM Nejad, ...
Journal of human genetics 58 (8), 526, 2013
|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
|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
|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
|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
|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
|PLA2G6-associated dystonia–parkinsonism: Case report and literature review|
S Karkheiran, GA Shahidi, RH Walker, C Paisan-Ruiz
Tremor and Other Hyperkinetic Movements 5, 2015
|A clinic‐based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients|
S Shojaee, F Sina, N Farboodi, Z Fazlali, F Ghazavi, SA Ghorashi, ...
Movement Disorders 24 (7), 1023-1027, 2009
|Restless legs syndrome in Iranian patients with multiple sclerosis|
S Miri, M Rohani, MA Sahraian, B Zamani, GA Shahidi, A Sabet, ...
Neurological Sciences 34 (7), 1105-1108, 2013
|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
|Quality of life in patients with Parkinson’s disease: translation and psychometric evaluation of the Iranian version of PDQ-39|
M Nojomi, Z Mostafavian, GA Shahidi, C Jenkinson
Journal of research in medical sciences: the official journal of Isfahan …, 2010
|Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population|
L Haghnejad, B Emamalizadeh, J Jamshidi, AZ Bidoki, H Ghaedi, ...
Journal of the neurological sciences 355 (1-2), 72-74, 2015