| Inborn errors of metabolism underlying primary immunodeficiencies N Parvaneh, P Quartier, P Rostami, JL Casanova, P de Lonlay Journal of clinical immunology 34, 753-771, 2014 | 29 | 2014 |
| Role of vitamin D and vitamin D receptor gene polymorphisms on residual beta cell function in children with type 1 diabetes mellitus N Habibian, MM Amoli, F Abbasi, A Rabbani, A Alipour, F Sayarifard, ... Pharmacological Reports 71, 282-288, 2019 | 27 | 2019 |
| Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations AR Tavasoli, N Parvaneh, MR Ashrafi, Z Rezaei, J Zschocke, P Rostami Orphanet Journal of Rare Diseases 13, 1-8, 2018 | 20 | 2018 |
| Endocrine complications in patients with major β-thalassemia P Rostami, G Hatami, A Shirkani Iranian South Medical Journal 14 (4), 240-245, 2011 | 20 | 2011 |
| The first report of relative incidence of inherited white matter disorders in an Asian country based on an Iranian bioregistry system MR Ashrafi, Z Rezaei, M Heidari, S Nikbakht, RA Malamiri, M Mohammadi, ... Journal of Child Neurology 33 (4), 255-259, 2018 | 17 | 2018 |
| Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature review P Rostami, S Hosseinpour, MR Ashrafi, H Alizadeh, M Garshasbi, ... Acta Neurologica Belgica 120, 511-516, 2020 | 16 | 2020 |
| A randomized clinical trial of insulin glargine and aspart, compared to NPH and regular insulin in children with Type 1 diabetes mellitus P Rostami, A Setoodeh, A Rabbani, M Nakhaei-Moghadam, ... Iranian Journal of Pediatrics 24 (2), 173, 2014 | 10 | 2014 |
| Early infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: a case report and literature review AR Tavasoli, RS Badv, J Zschocke, MR Ashrafi, P Rostami Brain and Development 39 (8), 714-716, 2017 | 9 | 2017 |
| Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b) M Eghbali, M Abiri, S Talebi, Z Noroozi, M Shakiba, P Rostami, ... Orphanet Journal of Rare Diseases 15, 1-11, 2020 | 8 | 2020 |
| Molecular investigation of mutations in androgen receptor and 5‐alpha‐reductase‐2 genes in 46, XY Disorders of Sex Development with normal testicular development M Ahmadifard, A Kajbafzadeh, S Panjeh‐Shahi, F Vand‐Rajabpour, ... Andrologia 51 (5), e13250, 2019 | 8 | 2019 |
| Stimulated and unstimulated saliva glucose levels in children suffer insulin-dependent diabetes mellitus M Khayamzdeh, I Mirzaii-Dizgah, P Rostami, F Izadi, M Khayamzadeh, ... Annals of Military and Health Sciences Research 15 (2), 2017 | 8 | 2017 |
| Neurological and vascular manifestations of ethylmalonic encephalopathy AR Tavasoli, P Rostami, MR Ashrafi, P Karimzadeh Iranian journal of child neurology 11 (2), 57, 2017 | 8 | 2017 |
| AGPAT2 gene mutation in a child with Berardinelli-Seip congenital lipodystrophy syndrome P Rostami, M Nakhaeimoghadam, FM Bijani, A Sotoudeh, A Rabbani, ... Annales d'endocrinologie 74 (1), 59-61, 2013 | 8 | 2013 |
| 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 | 7 | 2021 |
| Pericentric inversion of chromosome 9 in an infant with ambiguous genitalia A Sotoudeh, P Rostami, M Nakhaeimoghadam, R Mohsenipour, N Rezaei Acta Medica Iranica, 655-657, 2017 | 7 | 2017 |
| Status of bone mineral density in children with type 1 diabetes mellitus and its related factors F Sayarifard, M Safarirad, A Rabbani, A Sayarifard, V Ziaee, A Setoodeh, ... Iranian Journal of Pediatrics 27 (4), 2017 | 6 | 2017 |
| Insulin edema in a child with diabetes mellitus type 1 P Rostami, A Sotoudeh, M Nakhaeimoghadam, A Rabbani, N Rezaei The Turkish Journal of Pediatrics 54 (3), 309, 2012 | 6 | 2012 |
| Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel … A Setoodeh, S Panjeh-Shahi, F Bahmani, F Vand-Rajabpour, N Jalilian, ... Orphanet Journal of Rare Diseases 17 (1), 10, 2022 | 4 | 2022 |
| Prevalence of dental abnormalities in different calcium metabolism disorders in a group of Iranian children R Mohsenipour, A Mohebbi, P Rostami, A Fallahi, P Rahmani Biomed. Res 28, 6757-6762, 2017 | 4 | 2017 |
| Methylmalonic acidemia with emergency hypertension B Yaghmaei, P Rostami, FN Varzaneh, B Gharib, B Bazargani, N Rezaei Nefrología (English Edition) 36 (1), 75-76, 2016 | 4 | 2016 |
