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Page 1
Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15).
Hemoglobin. 2019 Jul-Sep;43(4-5):223-228. doi: 10.1080/03630269.2019.1675689. Epub 2019 Oct 11.
Hemoglobin. 2019.
PMID: 31603010
Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia.
Casini A, von Mackensen S, Santoro C, Djambas Khayat C, Belhani M, Ross C, Dorgalaleh A, Naz A, Ünal E, Abdelwahab M, Lozeron ED, Trillot N, Susen S, Peyvandi F, de Moerloose P; QualyAfib Study Group.
Casini A, et al.
Blood. 2021 Jun 3;137(22):3127-3136. doi: 10.1182/blood.2020009472.
Blood. 2021.
PMID: 33512441
Free article.
Clinical Trial.
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HPA antibodies in Algerian multitransfused patients: Prevalence and involvement in platelet refractoriness.
Brouk H, Bertrand G, Zitouni S, Djenouni A, Martageix C, Griffi F, Kaplan C, Ouelaa H.
Brouk H, et al. Among authors: djenouni a.
Transfus Apher Sci. 2015 Jun;52(3):295-9. doi: 10.1016/j.transci.2014.12.028. Epub 2014 Dec 30.
Transfus Apher Sci. 2015.
PMID: 25620758
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History and structures of telecommunication in pathology, focusing on open access platforms.
Kayser K, Borkenfeld S, Djenouni A, Kayser G.
Kayser K, et al. Among authors: djenouni a.
Diagn Pathol. 2011 Nov 7;6:110. doi: 10.1186/1746-1596-6-110.
Diagn Pathol. 2011.
PMID: 22059444
Free PMC article.
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The World Federation of Hemophilia World Bleeding Disorders Registry: insights from the first 10,000 patients.
Coffin D, Gouider E, Konkle B, Hermans C, Lambert C, Diop S, Ayoub E, Tootoonchian E, Youttananukorn T, Dakik P, Pereira T, Iorio A, Pierce GF; World Bleeding Disorders Registry Participating Investigators.
Coffin D, et al.
Res Pract Thromb Haemost. 2023 Nov 20;7(8):102264. doi: 10.1016/j.rpth.2023.102264. eCollection 2023 Nov.
Res Pract Thromb Haemost. 2023.
PMID: 38193052
Free PMC article.
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