|Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity|
neurogenetics 7 (3), 149-156, 2006
|Genetics of intellectual disability in consanguineous families|
H Hu, K Kahrizi, L Musante, Z Fattahi, R Herwig, M Hosseini, C Oppitz, ...
Molecular psychiatry 24 (7), 1027-1039, 2019
|Efficacy of the Atkins diet as therapy for intractable epilepsy in children|
SH Tonekaboni, P Mostaghimi, P Mirmiran, A Abbaskhanian, ...
ARCHIVES OF IRANIAN MEDICINE 13 (6), 492-497, 2010
|Neurocognitive effects of phenobarbital discontinuation in epileptic children|
SH Tonekaboni, N Beyraghi, HS Tahbaz, SA Bahreynian, ...
Epilepsy & Behavior 8 (1), 145-148, 2006
|Closed-loop neurostimulators: A survey and a seizure-predicting design example for intractable epilepsy treatment|
H Kassiri, S Tonekaboni, MT Salam, N Soltani, K Abdelhalim, ...
IEEE transactions on biomedical circuits and systems 11 (5), 1026-1040, 2017
|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
|GM2-Gangliosidosis (Sandhoff and Tay Sachs disease): diagnosis and neuroimaging findings (an Iranian pediatric case series)|
P Karimzadeh, N Jafari, HN Biglari, SJ Dari, FA Abadi, MR Alaee, ...
Iranian journal of child neurology 8 (3), 55, 2014
|Effects of miglustat on stabilization of neurological disorder in Niemann–Pick disease type C: Iranian pediatric case series|
P Karimzadeh, SH Tonekaboni, MR Ashrafi, Y Shafeghati, A Rezayi, ...
Journal of child neurology 28 (12), 1599-1606, 2013
|Bone mineral density in ambulatory children with epilepsy|
O Yaghini, SH Tonekaboni, SMA Shahkarami, FA Abadi, F Shariat, ...
The Indian Journal of Pediatrics 82 (3), 225-229, 2015
|Evaluating the validity and reliability of PDQ-II and comparison with DDST-II for two step developmental screening|
S Shahshahani, F Sajedi, N Azari, R Vameghi, A Kazemnejad, ...
Iranian journal of pediatrics 21 (3), 343, 2011
|Neurodegeneration with brain iron accumulation: an overview|
SH TONEKABONI, M MOLLAMOHAMMADI
Iranian journal of child neurology 8 (4), 1, 2014
|The Ketogenic and Atkins diets effect on intractable epilepsy: A comparison|
A Ghazavi, SH Tonekaboni, P Karimzadeh, AA Nikibakhsh, A Khajeh, ...
Iranian journal of child neurology 8 (3), 12, 2014
|Anxiety and depression in patients admitted in cardiac care unit, Taleghanihospital, Tehran, Iran, 2003|
N Beyraghi, SH Tonekaboni, GH Vakili
Hormozgan Medical Journal 9 (4), 261-264, 2006
|Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group|
F Al Jasmi, M Al Jumah, F Alqarni, N Al-Sanna’a, F Al-Sharif, S Bohlega, ...
BMC neurology 15 (1), 205, 2015
|Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping|
JS Amos, L Huang, J Thevenon, A Kariminedjad, CL Beaulieu, ...
Clinical genetics 91 (1), 92-99, 2017
|Use of complementary and alternative medicine for epileptic children in Tehran: a cross-sectional study (2009-2011)|
SH Tonekaboni, SJ NAEINI, A KHAJEH, O YAGHINI, A GHAZAVI, ...
Iranian journal of child neurology 8 (1), 26, 2014
|Methylmalonic acidemia: diagnosis and neuroimaging findings of this neurometabolic disorder (an Iranian pediatric case series)|
P KARIMZADEH, N JAFARI, FA ABADI, S JABBEDARI, MM TAGHDIRI, ...
Iranian journal of child neurology 7 (3), 63, 2013
|Efficacy of levetiracetam in children with refractory epilepsy as an add-on trial|
SH Tonekaboni, M Ghazavi, P Karimzadeh, F Mahvelati, M Ghofrani
Epilepsy research 90 (3), 273-277, 2010
|Knowledge, attitudes, and practices among mothers of children with epilepsy: A study in a teaching hospital|
AA Kolahi, M Abbasi-Kangevari, P Bakhshaei, F Mahvelati-Shamsabadi, ...
Epilepsy & Behavior 69, 147-152, 2017
|Eight novel mutations in MLC1 from 18 Iranian patients with megalencephalic leukoencephalopathy with subcortical cysts|
A Kariminejad, A Rajaee, MR Ashrafi, H Alizadeh, SH Tonekaboni, ...
European journal of medical genetics 58 (2), 71-74, 2015