Autoimmune phenotype in patients with common variable immunodeficiency H Abolhassani, D Amirkashani, N Parvaneh, P Mohammadinejad, ... J Investig Allergol Clin Immunol 23 (5), 323-9, 2013 | 80 | 2013 |
Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations L Youssefian, H Vahidnezhad, AH Saeidian, S Pajouhanfar, S Sotoudeh, ... Journal of hepatology 71 (2), 366-370, 2019 | 50 | 2019 |
Evaluation of near final height in boys with constitutional delay in growth and puberty F Rohani, MR Alai, S Moradi, D Amirkashani Endocrine connections 7 (3), 456-459, 2018 | 18 | 2018 |
The prevalence of zinc deficiency in morbidly obese patients before and after different types of bariatric surgery F Soheilipour, M Ebrahimian, M Pishgahroudsari, M Hajian, ... BMC endocrine disorders 21, 1-7, 2021 | 17 | 2021 |
Placenta derived Mesenchymal Stem Cells transplantation in Type 1 diabetes: preliminary report of phase 1 clinical trial S Madani, A Setudeh, HR Aghayan, S Alavi-Moghadam, M Rouhifard, ... Journal of Diabetes & Metabolic Disorders 20, 1179-1189, 2021 | 9 | 2021 |
Mycobacterium tuberculosis meningitis as the first presentation of chronic granulomatous disease G Khotaei, A Hirbod-Mobarakeh, D Amirkashani, F Manafi, N Rezaei Brazilian Journal of Infectious Diseases 16, 491-492, 2012 | 9 | 2012 |
A new case of Chanarin-Dorfman Syndrome with a novel deletion in ABHD5 gene S Nakhaei, H Heidary, A Rahimian, M Vafadar, F Roohani, GR Bahoosh, ... Iranian Biomedical Journal 22 (6), 415, 2018 | 8 | 2018 |
Fertility assessment in thalassemic men S Ansari, A Kiumarsi, A Azarkeivan, MM Allameh, DA Kashani, MR Azar Thalassemia Reports 7 (1), 6362, 2017 | 5 | 2017 |
A novel mutation in the OXCT1 gene causing Succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency starting with neurologic manifestations D Amirkashani, M Asadollahi, R Hosseini, S Talebi, Z Golchehre, ... Iranian Journal of Child Neurology 17 (2), 127, 2023 | 4 | 2023 |
Estrogen replacement therapy: effects of starting age on final height of girls with chronic kidney disease and short stature D Amirkashani, F Rohani, M Khodadost, R Hoseini, H Alidoost, S Madani Bmc Pediatrics 22 (1), 355, 2022 | 4 | 2022 |
Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion) SR Ghaffari, M Rafati, M Shadnoush, S Pourbabaee, M Aghighi, ... Human Mutation 43 (4), e1-e23, 2022 | 4 | 2022 |
Methenyltetrahydrofolate synthease deficiency (MTHFS deficiency): novel mutation and brain MRI findings: A case report and glance to other cases M Vafaee-Shahi, D Amirkashani, MR Ashrafi, L Tahernia, A Riahi Clinical Neurology and Neurosurgery 215, 107153, 2022 | 3 | 2022 |
The 5th International Congress of Iranian Pediatric Nephrology Association M Mohkam Journal of Pediatric Nephrology 4 (2), 1-60, 2016 | 3 | 2016 |
Acute disseminated encephalomyelitis mimicking acute meningoencephalitis RA Mahmoud, A Davood, HM Armin, Y Bahareh, T Alireza, M Farzad Acta clinica Croatica 52 (4.), 523-528, 2013 | 2 | 2013 |
Pseudodendritic keratitis in citrullinemia; a report of an unusual and novel ocular finding in this metabolic disorder D Amirkashani, S Talebi, A Zekri, P Abdi, M Mehramiz American Journal of Ophthalmology Case Reports 34, 102044, 2024 | 1 | 2024 |
Revision of sex hormone replacement therapy for CKD Pediatric cases D Amirkashani, S Madani Journal of Diabetes & Metabolic Disorders 22 (1), 897-898, 2023 | 1 | 2023 |
A new scoring system for stratifying risk for cerebral edema in children suffering diabetic ketoacidosis B Haghighi Aski, A Manafi Anari, N Sarejloo, F Abolhassan Choobdar, ... International Journal of Children and Adolescents 5 (2), 0-0, 2019 | 1 | 2019 |
The effect of bisphosphonate with and without testosterone on bone mineral density in male patients with Beta-Thalassemia major S Ansari Damavandi, D Amirkashani, M Tagrian Journal of Clinical Care and Skills 5 (3), 1001-1012, 2024 | | 2024 |
The Effect of Bisphosphonate with Testosterone on Bone Mineral Density in Male Patients with Thalassemia Major S Ansari Damavandi, D Amirkashani, M Tagrian Isfahani Journal of Clinical Care and Skills 5 (3), 165-171, 2024 | | 2024 |
A Case Report About One Patient with Citrullinemia Type I with Classic Bartter Syndrome Simultaneously D Amirkashani, S Dadakhani Zahedan Journal of Research in Medical Sciences 26 (3), 2024 | | 2024 |