Berber E - Search Results

1

Gene therapy in haemophilia: literature review and regional perspectives for Turkey.

Kavaklı K, Antmen B, Okan V, Şahin F, Aytaç S, Balkan C, Berber E, Kaya Z, Küpesiz A, Zülfikar B. Kavaklı K, et al. Among authors: berber e. Ther Adv Hematol. 2022 Jul 23;13:20406207221104591. doi: 10.1177/20406207221104591. eCollection 2022. Ther Adv Hematol. 2022. PMID: 35898436 Free PMC article. Review.

2

Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.

Colakoglu S, Bayhan T, Tavil B, Keskin EY, Cakir V, Gümrük F, Çetin M, Aytaç S, Berber E. Colakoglu S, et al. Among authors: berber e. Blood Transfus. 2018 Jan;16(1):105-113. doi: 10.2450/2016.0098-16. Epub 2016 Oct 4. Blood Transfus. 2018. PMID: 27723456 Free PMC article. Clinical Trial.

3

A common VWF exon 28 haplotype in the Turkish population.

Berber E, Pehlevan F, Akin M, Capan OY, Kavakli K, Çaglayan SH. Berber E, et al. Clin Appl Thromb Hemost. 2013 Sep;19(5):550-6. doi: 10.1177/1076029612441054. Epub 2012 Apr 2. Clin Appl Thromb Hemost. 2013. PMID: 22473027 Free article.

4

R506Q (FV Leiden) and R485K Mutations in the Factor V Gene: Incidence in Deep Venous Thrombosis and Hemophilia A Patients.

Berber E, Kavaklı K, Akar N, Berber E, Çağlayan SH. Berber E, et al. Turk J Haematol. 2003 Dec 5;20(4):221-5. Turk J Haematol. 2003. PMID: 27263518 English.

5

Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.

Kılıç SÇ, İçağasıoğlu FD, Güven AS, Berber E. Kılıç SÇ, et al. Among authors: berber e. Blood Transfus. 2014 Jul;12(3):446-8. doi: 10.2450/2014.0022-14. Blood Transfus. 2014. PMID: 25074526 Free PMC article. No abstract available.

6

Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p.M771I, p.L881R and p.P1413L.

Berber E, Ozbil M, Brown C, Baslar Z, Caglayan SH, Lillicrap D. Berber E, et al. Blood Transfus. 2017 Oct;15(6):548-556. doi: 10.2450/2016.0034-16. Epub 2016 Jul 25. Blood Transfus. 2017. PMID: 27483487 Free PMC article.

7

Molecular characterization of FXI deficiency.

Berber E. Berber E. Clin Appl Thromb Hemost. 2011 Feb;17(1):27-32. doi: 10.1177/1076029609355587. Epub 2010 Mar 22. Clin Appl Thromb Hemost. 2011. PMID: 20308231 Free article.

8

Characterization of the genetic basis of FXI deficiency in two Turkish patients.

Berber E, Rimoldi V, Usluer S, Aksu S, Pekcelen Y, Cağlayan SH, Duga S. Berber E, et al. Haemophilia. 2010 May;16(3):564-6. doi: 10.1111/j.1365-2516.2009.02152.x. Epub 2009 Dec 14. Haemophilia. 2010. PMID: 20015217 No abstract available.

9

Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.

Berber E, Fidanci ID, Un C, El-Maarri O, Aktuglu G, Gurgey A, Celkan T, Meral A, Oldenburg J, Graw J, Akar N, Caglayan H. Berber E, et al. Haemophilia. 2006 Jul;12(4):398-400. doi: 10.1111/j.1365-2516.2006.01302.x. Haemophilia. 2006. PMID: 16834740

10

Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter.

Hough C, Cameron CL, Notley CR, Brown C, O'Brien L, Keightley AM, Berber E, Lillicrap D. Hough C, et al. Among authors: berber e. J Thromb Haemost. 2008 Jul;6(7):1183-90. doi: 10.1111/j.1538-7836.2008.03011.x. Epub 2008 Jul 1. J Thromb Haemost. 2008. PMID: 18485092 Free article.

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