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Year Number of Results
2007 1
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2012 2
2013 8
2014 6
2015 13
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2017 7
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2019 6
2020 10
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2022 4
2023 5
2024 2

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Page 1
Inherited Platelet Function Disorders (IPFDs).
Dorgalaleh A, Tabibian S, Shamsizadeh M. Dorgalaleh A, et al. Among authors: tabibian s. Clin Lab. 2017 Jan 1;63(1):1-13. doi: 10.7754/Clin.Lab.2016.160607. Clin Lab. 2017. PMID: 28164499 Review.
Intracranial hemorrhage in congenital bleeding disorders.
Tabibian S, Motlagh H, Naderi M, Dorgalaleh A. Tabibian S, et al. Blood Coagul Fibrinolysis. 2018 Jan;29(1):1-11. doi: 10.1097/MBC.0000000000000660. Blood Coagul Fibrinolysis. 2018. PMID: 28901996 Review.
Molecular basis of rare congenital bleeding disorders.
Dorgalaleh A, Bahraini M, Shams M, Parhizkari F, Dabbagh A, Naderi T, Fallah A, Fazeli A, Ahmadi SE, Samii A, Daneshi M, Heydari F, Tabibian S, Tavasoli B, Noroozi-Aghideh A, Tabatabaei T, Gholami MS. Dorgalaleh A, et al. Among authors: tabibian s. Blood Rev. 2023 May;59:101029. doi: 10.1016/j.blre.2022.101029. Epub 2022 Nov 9. Blood Rev. 2023. PMID: 36369145 Review.
Diagnosis of factor XIII deficiency.
Dorgalaleh A, Tabibian S, Hosseini MS, Farshi Y, Roshanzamir F, Naderi M, Kazemi A, Zaker F, Aghideh AN, Shamsizadeh M. Dorgalaleh A, et al. Among authors: tabibian s. Hematology. 2016 Aug;21(7):430-9. doi: 10.1080/10245332.2015.1101975. Epub 2016 Mar 30. Hematology. 2016. PMID: 27077776 Review.
How to Assess Founder Effect in Patients with Congenital Factor XIII Deficiency.
Shahraki H, Dorgalaleh A, Fathi M, Tabibian S, Teimourian S, Mollanoori H, Khiabani A, Zaker F. Shahraki H, et al. Among authors: tabibian s. Int J Hematol Oncol Stem Cell Res. 2020 Oct 1;14(4):265-273. doi: 10.18502/ijhoscr.v14i4.4480. Int J Hematol Oncol Stem Cell Res. 2020. PMID: 33603988 Free PMC article. Review.
78 results