| Hemodialysis adequacy and treatment in Iranian patients a national multicenter study MR RASOULI, E POURBAKHTYARAN, M AMINI, M AGHIGHI, ... IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD) 5 (2), 103-109, 2011 | 69 | 2011 |
| Acute pancreatitis as a possible unusual manifestation of COVID‐19 in children N Bineshfar, A Mirahmadi, F Karbasian, E Pourbakhtyaran, A Karimi, ... Case Reports in Pediatrics 2021 (1), 6616211, 2021 | 17 | 2021 |
| A review on the clinical guidelines on pediatric traumatic brain injury FK Hojjat Derakhshanfar, Elham Pourbakhtyaran, Samane Rahimi, Samira Sayyah ... Eur J Transl Myol 30 (1), 2019 | 14* | 2019 |
| Harmonic scalpel is more secure than conventional methods in total thyroidectomy: a randomized clinical trial A Soroush, E Pourbakhtyaran, S Allame, MM Zamani, M Etemadi, S Nasiri J Minim Invasive Surg Sci 2 (3), 23-7, 2013 | 11 | 2013 |
| Epilepsia partialis continua a clinical feature of a missense variant in the ADCK3 gene and poor response to therapy MR Ashrafi, R Haghighi, RS Badv, H Ghabeli, AR Tavasoli, ... Journal of Molecular Neuroscience 72 (5), 1125-1132, 2022 | 9 | 2022 |
| Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation (ROHHAD) syndrome: a case report B Bagheri, E Pourbakhtyaran, FT Kiasari, B Taherkhanchi, S Salarian, ... Archives of Pediatric Infectious Diseases 5 (1), 2017 | 9 | 2017 |
| Stroke modifies drug consumption in opium addicts: role of the insula Y Yousefzadeh-Fard, MH Gharedaghi, S Esmaeili, E Pourbakhtyaran, ... Basic and clinical neuroscience 4 (4), 307, 2013 | 9 | 2013 |
| Primary and secondary microcephaly, global developmental delay, and seizure in two siblings caused by a novel missense variant in the ZNF335 gene AR Tavasoli, EHE Memar, MR Ashrafi, SMM Hosseini, R Haghighi, ... Journal of Molecular Neuroscience 72 (4), 719-729, 2022 | 8 | 2022 |
| Renal involvement in COVID-19 among Iranian children M Mohkam, M Mirzaee, FA Gorgi, SR Tabatabaei, A Karimi, S Armin, ... Archives of Pediatric Infectious Diseases 9 (1), 2021 | 8 | 2021 |
| Is It Stevens–Johnson Syndrome or MIS‐C with Mucocutaneous Involvement? A Karimi, E Pourbakhtiaran, M Fallahi, F Karbasian, S Armin, D Babaie Case reports in pediatrics 2021 (1), 1812545, 2021 | 6 | 2021 |
| Childhood Guillain–Barre syndrome in the SARS‐CoV‐2 era: Is there any causative relation? E Pourbakhtyaran, M Heidari, MG Akbari, M Mohammadi, RS Badv, ... Clinical Case Reports 10 (12), e6772, 2022 | 5 | 2022 |
| Succinate dehydrogenase deficiency: a treatable neurometabolic disorder P Karimzadeh, M Keramatipour, A Karamzade, E Pourbakhtyaran Iranian Journal of Child Neurology 14 (4), 111, 2020 | 3 | 2020 |
| The 5th International Congress of Iranian Pediatric Nephrology Association M Mohkam Journal of Pediatric Nephrology 4 (2), 1-60, 2016 | 3 | 2016 |
| Current evidence on the adverse effects of sodium bicarbonate used in bread processing on human health: A systematic review E Pourbakhtyaran, MH Sowlat, A Rashidian, P Pasalar, N Rastkari, ... Iranian Journal of Epidemiology 8 (4), 31-39, 2013 | 3 | 2013 |
| Stroke modifies drug consumption in opium addicts: role of the insula FY YOUSEFZADEH, MH GHAREDAGHI, S ESMAEILI, ... Basic and Clinical Neuroscience 4 (4), 29-36, 2013 | 3 | 2013 |
| The quality of life in children with spinal muscular atrophy: a case–control study G Zamani, MR Ashrafi, H Ghabeli, MG Akbari, M Mohammadi, RS Badv, ... BMC pediatrics 22 (1), 708, 2022 | 2 | 2022 |
| Primary spinal tumors and masses in children A Farzan, P Ahmadi, E Tasdighi, MR Zinatzadeh, E Pourbakhtyaran Iranian journal of child neurology 16 (2), 129, 2022 | 2 | 2022 |
| Expanding the neuroimaging findings of guanidinoacetate methyltransferase deficiency in an Iranian girl with a homozygous frameshift variant in the GAMT SA Afjei, MF Mohammadi, E Pourbakhtyaran, H Ghabeli, MR Ashrafi, ... neurogenetics 24 (2), 67-78, 2023 | 1 | 2023 |
| A Retrospective Single-center Study of Presentation and Prognosis of Guillain-Barré Syndrome in Pediatric Patients M Nasehi, P Ahmadi, Z Khalili, M Rahmannia, Z Ahmadi, MR Zitatzadeh, ... Iranian Journal of Pediatrics 33 (1), 2023 | 1 | 2023 |
| Genetic analysis of forty MLPA-negative Duchenne muscular dystrophy patients by whole-exome sequencing GR Zamani, MF Mohammadi, AR Tavasoli, MR Ashrafi, S Hosseinpour, ... Journal of Molecular Neuroscience 72 (5), 1098-1107, 2022 | 1 | 2022 |
Fereshteh KarbasianDepartment of pediatric gastroenterology and hepatology,Iran university of medical sciences在 sbmu.ac.ir 的电子邮件经过验证
