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Acta Oncologica (Stockholm, Sweden)|November 12, 2014
Impact of changing rectal dose volume parameters over time on late rectal and urinary toxicity after high-dose intensity-modulated radiotherapy for prostate cancer: A 10-years single centre experienceValérie Fonteyne, Simin Sadeghi, Piet Ost, et al.
Health Science Reports|April 20, 2026
Association of S100B Serum Level With Postoperative Cognitive Dysfunction (POCD) in Non-Cardiac Surgery: A Meta-Analysis StudySaba Asefi, Pouya Omidi, Kimia Jazi, et al.
Journal of Psychosocial Oncology|April 14, 2026
A comparison of breast cancer screening beliefs and barriers among Afghan and Syrian refugee womenFatin Atrooz, Chiara Acquati, Jenna Zamil, et al.
Nucleosides, Nucleotides & Nucleic Acids|January 4, 2017
Evaluation of functional RAGE gene polymorphisms in childhood acute lymphoblastic leukemia-A case-control study from IranEbrahim Eskandari-Nasab, Mohammad Hashemi, Seyed-Shahab-Adin Hasani, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|December 3, 2014
Rectal toxicity after intensity modulated radiotherapy for prostate cancer: which rectal dose volume constraints should we use?Valérie Fonteyne, Piet Ost, Frank Vanpachtenbeke, et al.
Pediatric Hematology and Oncology|October 19, 2013
A prospective study of tubular dysfunction in pediatric patients with Beta thalassemia major receiving deferasiroxMajid Naderi, Simin Sadeghi-Bojd, Ali Kord Valeshabad, et al.
CEN Case Reports|March 26, 2023
Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literatureFarnaz Kamali, Mahnaz Jamee, John A Sayer, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|July 16, 2019
Correlation of bleeding score with frequency and severity of bleeding symptoms in FXIII deficiency assessing by the ISTH Bleeding Assessment ToolMajid Naderi, Nader Cohan, Sezaneh Haghpanah, et al.
Orphanet Journal of Rare Diseases|February 15, 2019
Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosisMaryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, et al.
Frontiers in Pediatrics|April 6, 2019
A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle EastMaryam Najafi, Dor Mohammad Kordi Tamandani, Anoush Azarfar, et al.
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