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209 results

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Page 1
Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE-diagnosis study (IMPRESsion).
Ghaffari SR, Rafati M, Shadnoush M, Pourbabaee S, Aghighi M, Mirab Samiee S, Kermanchi J, Alaei MR, Salehpour S, Amirkashani D, Setoodeh A, Sarkhail P, Badv RS, Aminzadeh M, Shiva S, Eshraghi P, Moravej H, Hashemipour M, Rostampour N, Hamidieh AA, Shamsian BS, Shams S, Zamanfar D, Ebrahimi A, Otadi A, Tara SZ, Barati Z, Fakhri L, Hoseini A, Amiri H, Ramandi S, Mostofinezhad N, Kani ZP, Mohammadyari E, Khosravi M, Saadati M, Hoseininasab F, Khorram Khorshid HR, Modaberisaber Y. Ghaffari SR, et al. Among authors: hashemipour m. Hum Mutat. 2022 Apr;43(4):e1-e23. doi: 10.1002/humu.24328. Epub 2022 Feb 3. Hum Mutat. 2022. PMID: 35005816
Optimal Frequency to Screen Celiac Disease amongst Patients with Type 1 Diabetes Mellitus: A Multicenter Study.
Moravej H, Zamanfar D, Aghamahdi F, Hashemipour M, Mirrashidi FS, Ghaemi N, Eshraghi P, Ilkhanipoor H, Amirhakimi A, Yazdani N, Asl SN, Hashemian S, Raoofat A, Vazirian MV, Ebrahimzadeh H. Moravej H, et al. Among authors: hashemipour m. Prim Care Diabetes. 2021 Dec;15(6):1100-1103. doi: 10.1016/j.pcd.2021.08.011. Epub 2021 Sep 6. Prim Care Diabetes. 2021. PMID: 34503936
Prevalence of nephrocalcinosis in children with congenital adrenal hyperplasia.
Madihi Y, Mostofizadeh N, Shamsipour Dehkordi H, Riahinezhad M, Hovsepian S, Rostampour N, Dehkodi EH, Mehrkash M, Momen T, Hashemipour M. Madihi Y, et al. Among authors: hashemipour m. J Res Med Sci. 2022 Feb 18;27:16. doi: 10.4103/jrms.jrms_872_21. eCollection 2022. J Res Med Sci. 2022. PMID: 35342446 Free PMC article.
New molecular insights into the A218V variant impact on the steroidogenic acute regulatory protein (STAR) associated with 46, XY disorders of sexual development.
Aghaei S, Farrokhi E, Saffari-Chaleshtori J, Hoseinzadeh M, Molavi N, Hashemipour M, Rostampour N, Asgharzadeh S, Tabatabaiefar MA. Aghaei S, et al. Among authors: hashemipour m. Mol Genet Genomics. 2023 May;298(3):693-708. doi: 10.1007/s00438-023-02006-4. Epub 2023 Apr 1. Mol Genet Genomics. 2023. PMID: 37004560
Evaluation of cardiac findings in mucopolysaccharidosis.
Dehghan B, Rostampour N, Sedighi M, Saryazdi MH, Rizi MJ, Mostofizadeh N, Hashemipour M, Khoshhali M. Dehghan B, et al. Among authors: hashemipour m. Int J Cardiovasc Imaging. 2024 Jan;40(1):73-78. doi: 10.1007/s10554-023-02983-y. Epub 2023 Oct 17. Int J Cardiovasc Imaging. 2024. PMID: 37845409
Quality of Life in Patients with Phenylketonuria: A Systematic Review.
Jahangiri Z, Rostampour N, Hovsepian S, Chegini R, Hashemipour M. Jahangiri Z, et al. Among authors: hashemipour m. Adv Biomed Res. 2024 Feb 26;13:15. doi: 10.4103/abr.abr_238_23. eCollection 2024. Adv Biomed Res. 2024. PMID: 38525399 Free PMC article. Review.
Evaluation of the safety and efficacy of biosimilar recombinant growth hormone in children with growth hormone deficiency: non-inferiority, randomized, parallel, multicentric and Phase III trial.
Zaeri H, Omidvar S, Servatian N, Arefnia S, Khademolreza N, Amini H, Taghavi B, Hashemipour M, Eshraghi P, Ghasemi M, Ghergherehchi R, Maleki E, Moravej H, Noorian S, Soheilipour F, Dalili S, Kharazmi H, Didban A, Akhlaghi A, Ghaznavi S, Shahbazi M. Zaeri H, et al. Among authors: hashemipour m. Expert Opin Drug Saf. 2024 May 8:1-9. doi: 10.1080/14740338.2024.2348576. Online ahead of print. Expert Opin Drug Saf. 2024. PMID: 38682328
The role of ultrasonography in primary congenital hypothyroidism.
Hashemipour M, Rostampour N, Nasry P, Hovsepian S, Basiratnia R, Hekmatnia A, Shahkarami AH, Mehrabi A, Hadian R, Amini M. Hashemipour M, et al. J Res Med Sci. 2011 Sep;16(9):1122-8. J Res Med Sci. 2011. PMID: 22973380 Free PMC article.
209 results