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Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations.
Orphanet J Rare Dis. 2019 Apr 27;14(1):87. doi: 10.1186/s13023-019-1042-4.
Orphanet J Rare Dis. 2019.
PMID: 31029159
Free PMC article.
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.
Shirzadeh T, Saeidian AH, Bagherian H, Salehpour S, Setoodeh A, Alaei MR, Youssefian L, Samavat A, Touati A, Fallah MS, Vahidnezhad H, Karimipoor M, Azadmehr S, Raeisi M, Bandehi Sarhadi A, Zafarghandi Motlagh F, Jamali M, Zeinali Z, Abiri M, Zeinali S; Additional individual contributors.
Shirzadeh T, et al.
J Inherit Metab Dis. 2018 Nov;41(6):1159-1167. doi: 10.1007/s10545-018-0228-6. Epub 2018 Aug 29.
J Inherit Metab Dis. 2018.
PMID: 30159852
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Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations.
Abiri M, Saei H, Eghbali M, Karamzadeh R, Shirzadeh T, Sharifi Z, Zeinali S.
Abiri M, et al. Among authors: shirzadeh t.
Metab Brain Dis. 2019 Aug;34(4):1145-1156. doi: 10.1007/s11011-019-00435-y. Epub 2019 May 22.
Metab Brain Dis. 2019.
PMID: 31119508
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The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A.
Azadmehr S, Rahiminejad F, Zafarghandi Motlagh F, Jamali M, Ghazizadeh Tehrani P, Shirzadeh T, Bagherian H, Karimipoor M, Davoudi-Dehaghani E, Zeinali S.
Azadmehr S, et al. Among authors: shirzadeh t.
Arch Iran Med. 2021 Dec 1;24(12):887-896. doi: 10.34172/aim.2021.133.
Arch Iran Med. 2021.
PMID: 35014236
Free article.
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Genetic attributes of Iranian cystic fibrosis patients: the diagnostic efficiency of CFTR mutations in over a decade.
Hosseini Nami A, Kabiri M, Zafarghandi Motlagh F, Shirzadeh T, Fakhari N, Karimi A, Bagherian H, Jamali M, Younesikhah S, Shadman S, Zeinali R, Zeinali S.
Hosseini Nami A, et al. Among authors: shirzadeh t.
Front Genet. 2023 May 18;14:1140034. doi: 10.3389/fgene.2023.1140034. eCollection 2023.
Front Genet. 2023.
PMID: 37274793
Free PMC article.
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A study on musculoskeletal complaints and working postures in pathology specialists in Iran.
Rafeemanesh E, Khooei A, Niroumand S, Shirzadeh T.
Rafeemanesh E, et al. Among authors: shirzadeh t.
BMC Musculoskelet Disord. 2021 Dec 3;22(1):1012. doi: 10.1186/s12891-021-04870-w.
BMC Musculoskelet Disord. 2021.
PMID: 34861852
Free PMC article.
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Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher Patients.
Sardarpour N, Bagherian H, Zafarghandi Motlagh F, Shirzadeh T, Asnavandi S, Younesikhah S, Salehpour S, Setoodeh A, Alaei MR, Zeinali S.
Sardarpour N, et al. Among authors: shirzadeh t.
Int J Mol Cell Med. 2023;12(1):40-50. doi: 10.22088/IJMCM.BUMS.12.1.40.
Int J Mol Cell Med. 2023.
PMID: 37942259
Free PMC article.
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