| PD‐1/PD‐L1 pathway: basic biology and role in cancer immunotherapy A Salmaninejad, SF Valilou, AG Shabgah, S Aslani, M Alimardani, ... Journal of cellular physiology 234 (10), 16824-16837, 2019 | 394 | 2019 |
| Tumor-associated macrophages: role in cancer development and therapeutic implications A Salmaninejad, SF Valilou, A Soltani, S Ahmadi, YJ Abarghan, ... Cellular oncology 42, 591-608, 2019 | 185 | 2019 |
| The role of inflammatory cytokines and tumor associated macrophages (TAMs) in microenvironment of pancreatic cancer SF Valilou, M Keshavarz-Fathi, N Silvestris, A Argentiero, N Rezaei Cytokine & growth factor reviews 39, 46-61, 2018 | 113 | 2018 |
| Duchenne muscular dystrophy: an updated review of common available therapies A Salmaninejad, SF Valilou, H Bayat, N Ebadi, A Daraei, M Yousefi, ... International Journal of Neuroscience 128 (9), 854-864, 2018 | 62 | 2018 |
| Tumor Antigens SF Valilou, N Rezaei Vaccines for Cancer Immunotherapy. An Evidence-Based Review on Current …, 2018 | 13* | 2018 |
| First report of congenital short bowel syndrome in an Iranian patient caused by a mutation in the CLMP gene J Gharesouran, BS Esfahani, SF Valilou, M Moradi, MH Mousavi, ... Journal of Pediatric Genetics 8 (02), 073-080, 2019 | 10 | 2019 |
| Whole-exome sequencing identifies three candidate homozygous variants in a consanguineous Iranian family with autism spectrum disorder and skeletal problems S Farajzadeh Valilou, A Alavi, M Pashaei, S Ghasemi Firouzabadi, ... Molecular Syndromology 11 (2), 62-72, 2020 | 6 | 2020 |
| PTPN22 Gene Polymorphisms in Pediatric Systemic Lupus Erythematosus T Bahrami, SF Valilou, M Sadr, S Soltani, A Salmaninejad, E Soltaninejad, ... Fetal and pediatric pathology 39 (1), 13-20, 2020 | 5 | 2020 |
| A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy SF Valilou, JK Hagh, MS Asl, IA Rad, M Edizadeh, A Pooladi Clinical case reports 9 (8), 2021 | 3 | 2021 |
| Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability M Fattahi, A Bushehri, A Alavi, V Asghariazar, A Nozari, SG Firouzabadi, ... Gene, 144918, 2020 | 3 | 2020 |
| Chapter 10-Genetic vaccine for cancer SF Valilou, M Keshavarz-Fathi Vaccines for Cancer Immunotherapy; Rezaei, N., Keshavarz-Fathi, M., Eds, 129-143, 2018 | 3 | 2018 |
| Eighth case of Li‐Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype M Edizadeh, H Kaymakcalan, SF Valilou, Y Şahin American Journal of Medical Genetics Part A 191 (5), 1465-1469, 2023 | | 2023 |
| A novel 160Kb deletion identified in PCCA gene using whole exome sequencing in a patient with propionic acidemia SF Valilou, H Heydari, S Shohani, S Samadpour, H Abdi, JK Hagh, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 298-299, 2020 | | 2020 |
| HMGB1 polymorphisms in acute lymphoblastic leukemia E Rayzan, SF Valilou, MA Sadeghi, S Hemmati, H Farajifard, ... Authorea Preprints, 2020 | | 2020 |
| Chapter 5 - Strategy of Allogeneic and Autologous Cancer Vaccines S Farajzadeh Valilou, N Rezaei Vaccines for Cancer Immunotherapy: An Evidence-Based Review on Current …, 2018 | | 2018 |
Nima RezaeiTehran University of Medical Sciences; Universal Scientific Education and Research Network (USERN)在 tums.ac.ir 的电子邮件经过验证
