| 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 | 53 | 2014 |
| Bilirubin induced encephalopathy P Karimzadeh, M Fallahi, M Kazemian, NT Taleghani, S Nouripour, ... Iranian journal of child neurology 14 (1), 7, 2020 | 50 | 2020 |
| Disease characteristics, prognosis and miglustat treatment effects on disease progression in patients with Niemann-Pick disease Type C: an international, multicenter … M Pineda, K Juríčková, P Karimzadeh, M Kolnikova, V Malinova, JL Insua, ... Orphanet Journal of Rare Diseases 14, 1-10, 2019 | 42 | 2019 |
| Hypoglycemia-occipital syndrome: a specific neurologic syndrome following neonatal hypoglycemia? P Karimzadeh, S Tabarestani, M Ghofrani Journal of Child Neurology 26 (2), 152-159, 2011 | 42 | 2011 |
| Evaluation of lymphocyte transformation test results in patients with delayed hypersensitivity reactions following the use of anticonvulsant drugs Z Karami, M Mesdaghi, P Karimzadeh, M Mansouri, MM Taghdiri, ... International Archives of Allergy and Immunology 170 (3), 158-162, 2016 | 41 | 2016 |
| Low glycemic index treatment in pediatric refractory epilepsy: the first Middle East report P Karimzadeh, M Sedighi, M Beheshti, E Azargashb, M Ghofrani, ... Seizure 23 (7), 570-572, 2014 | 40 | 2014 |
| The management of dental waste in dental offices and clinics in Shiraz, Southern Iran M Danaei, P Karimzadeh, M Momeni, CJ Palenik, M Nayebi, V Keshavarzi, ... The international journal of occupational and environmental medicine 5 (1), 18, 2014 | 39 | 2014 |
| A Suspicion Index to aid screening of early-onset Niemann-Pick disease Type C (NP-C) M Pineda, E Mengel, H Jahnová, B Héron, J Imrie, CM Lourenço, ... BMC pediatrics 16, 1-10, 2016 | 38 | 2016 |
| Posterior reversible encephalopathy syndrome in pediatric hematologic-oncologic disease: literature review and case presentation MT Arzanian, BS Shamsian, P Karimzadeh, M Kajiyazdi, F Malek, ... Iranian Journal of Child Neurology 8 (2), 1, 2014 | 37 | 2014 |
| Antiepileptic drug-related adverse reactions and factors influencing these reactions P Karimzadeh, V Bakrani Iranian journal of child neurology 7 (3), 25, 2013 | 37 | 2013 |
| Accidental children poisoning with methadone: an Iranian pediatric sectional study S Jabbehdari, F Farnaghi, SF Shariatmadari, N Jafari, FF Mehregan, ... Iranian journal of child neurology 7 (4), 32, 2013 | 36 | 2013 |
| 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 | 30 | 2013 |
| Approach to neurometabolic diseases from a pediatric neurological point of view P Karimzadeh Iranian journal of child neurology 9 (1), 1, 2015 | 26 | 2015 |
| 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 | 26 | 2014 |
| 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 | 23 | 2015 |
| Comparison of propranolol and pregabalin for prophylaxis of childhood migraine: a randomised controlled trial MKB Bali, AA Rahbarimanesh, M Sadeghi, M Sedighi, P Karimzadeh, ... Acta Medica Iranica, 276-280, 2015 | 23 | 2015 |
| The clinical features and diagnosis of Canavan’s disease: a case series of Iranian patients P Karimzadeh, N Jafari, HN Biglari, E Rahimian, F Ahmadabadi, H Nemati, ... Iranian journal of child neurology 8 (4), 66, 2014 | 21 | 2014 |
| Atypical findings of Guillain-Barré syndrome in children P Karimzadeh, MKB Bali, MM Nasehi, SMT Otaghsara, M Ghofrani Iranian Journal of Child Neurology 6 (4), 17, 2012 | 20 | 2012 |
| Case reports of juvenile GM1 gangliosidosisis type II caused by mutation in GLB1 gene P Karimzadeh, S Naderi, F Modarresi, H Dastsooz, H Nemati, ... BMC medical genetics 18, 1-7, 2017 | 19 | 2017 |
| Biotinidase deficiency: a reversible neurometabolic disorder (an Iranian pediatric case series) P Karimzadeh, F Ahmadabadi, N Jafari, S Jabbehdari, MR Alaee, ... Iranian journal of child neurology 7 (4), 47, 2013 | 19 | 2013 |
Mansoureh ToghaTehran University of Medical SciencesVerified email at tums.ac.ir
