Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping by Amos, J.S., Huang, L., Thevenon, J., Kariminedjad, A., Beaulieu, C.L., Masurel‐Paulet, A., Najmabadi, H., Fattahi, Z., Beheshtian, M., Tonekaboni, S.H., Tang, S., Helbig, K.L., Alcaraz, W., Rivière, J.‐B., Faivre, L., Innes, A.M., Lebel, R.R., Boycott, K.M.

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Efficacy of levetiracetam in children with refractory epilepsy as an add-on trial by Tonekaboni, S.H, Ghazavi, M, Karimzadeh, P, Mahvelati, F, Ghofrani, M

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Neurocognitive effects of phenobarbital discontinuation in epileptic children by Hassan Tonekaboni, Seyed, Beyraghi, Narguess, Sahar Tahbaz, Hosseinzadeh, Abdolmajid Bahreynian, Seyed, Aghamohammadpoor, Mehran

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Prophylaxis of childhood migraine: topiramate versus propranolol by Tonekaboni, Seyed Hassan, Ghazavi, Ahad, Fayyazi, Afshin, Khajeh, Ali, Taghdiri, Mohammad Mahdi, Abdollah Gorji, Fatemeh, Azarghashb, Eznollah

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Sodium Channel Gene Mutations in Children with GEFS+ and Dravet Syndrome: A Cross Sectional Study by Tonekaboni, SH, Ebrahimi, A, Bali, Bakhshandeh, Taheri Otaghsara, SM, Houshmand, M, Nasehi, M M, Taghdiri, M M, Moghaddasi, M

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A Novel Mutation of GDAP1 Associated with Charcot-Marie-Tooth Disease in An Iranian Family by Mohammadi Pargoo, E, Aryani, O, Tonekaboni, SH, Yaghmaei, P, Kamalidehghan, B, Houshmand, M

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Evaluation of one hundred pediatric muscle biopsies during a 2-year period in mofid children and toos hospitals by Nilipor, Yalda, Shariatmadari, Fakhredin, Abdollah Gorji, Fatemeh, Rouzrokh, Mohsen, Ghofrani, Mohamad, Karimzadeh, Parvaneh, Taghdiri, Moahammad Mehdi, Delavarkasmaei, Hosein, Ahmadabadi, Farzad, Bakhshandeh Bali, Mohammad Kazem, Nemati, Hamid, Saket, Sasan, Jafari, Narges, Yaghini, Omid, Tonekaboni, Seyed Hasan

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