Ergul Berber
Istanbul, Turkey
Last Updated: 09/26/2026
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Found 9 publications
Gene therapy in haemophilia: literature review and regional perspectives for Turkey.
Journal: Therapeutic advances in hematology
Published: January 17, 2022
Whole exome sequencing reveals novel candidate gene variants for MODY.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: May 28, 2020
Exploring the role of miRNAs in the diagnosis of MODY3
Journal: Turkish journal of medical sciences
Published: June 20, 2018
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.
Journal: Blood transfusion = Trasfusione del sangue
Published: April 15, 2016
Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p.M771I, p.L881R and p.P1413L.
Journal: Blood transfusion = Trasfusione del sangue
Published: February 06, 2016
Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.
Journal: Blood transfusion = Trasfusione del sangue
Published: February 07, 2014
A common VWF exon 28 haplotype in the Turkish population.
Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
Published: April 05, 2012
Higher expression of the novel gene upregulated gene 4 in two acute lymphoblastic leukemia patients with poor prednisolone response.
Journal: Acta haematologica
Published: January 09, 2012
The molecular genetics of von Willebrand disease.
Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology
Published: November 14, 2011
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Last Updated: 09/26/2026