gholamali shahidi
gholamali shahidi
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Title
Cited by
Cited by
Year
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
2402013
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
2292008
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
892000
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
512013
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
492014
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
412015
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
382018
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
342013
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
332013
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
302014
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
292016
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), 526-530, 2013
282013
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
272016
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
272015
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
272014
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
272013
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
262015
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
252009
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
242016
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
242015
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