B. Pezeshkpoor

发表

Novel characterization of a breakpoint in F8: an individualized approach to gene analysis when PCR and MLPA results contradict

J. Oldenburg, O. el-Maarri, M. D. Williams, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Selective Modulation of the Protease Activated Protein C Using Exosite Inhibiting Aptamers.

J. Oldenburg, G. Mayer, Fabian Tolle, 2020, Nucleic acid therapeutics.

F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis

M. Jamil, Amit Sharma, J. Oldenburg, 2019, Front. Genet..

In silico and in vitro evaluation of the impact of mutations in non-severe haemophilia A patients on assay discrepancies

A. Biswas, H. Singer, J. Oldenburg, 2019, Annals of Hematology.

Haemophilia A mutations in patients with non-severe phenotype associated with a discrepancy between one-stage and chromogenic factor VIII activity assays

J. Oldenburg, D. Delev, A. Pavlova, 2014, Thrombosis and Haemostasis.

Genetic testing in bleeding disorders

J. Oldenburg, O. el-Maarri, D. Perry, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

Variants in FIX propeptide associated with vitamin K antagonist hypersensitivity: functional analysis and additional data confirming the common founder mutations

J. Oldenburg, A. Pavlova, S. Ulrich, 2018, Annals of Hematology.

Identification and functional characterization of a novel F5 mutation (Ala512Val, FVBonn) associated with activated protein C resistance

A. Biswas, J. Oldenburg, A. Pavlova, 2016, Journal of thrombosis and haemostasis : JTH.

Functional Characterization of Antithrombin Mutations by Monitoring of Thrombin Inhibition Kinetics

J. Oldenburg, A. Pavlova, B. Pezeshkpoor, 2021, International journal of molecular sciences.

Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients—A Single-Center Experience in Genetic Diagnosis

J. Oldenburg, A. Pavlova, S. Unal, 2021, Journal of clinical medicine.

Deep intronic ‘mutations’ cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA

T. Haaf, J. Oldenburg, O. el-Maarri, 2013, Journal of thrombosis and haemostasis : JTH.

Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine Clinical Practice

J. Oldenburg, A. Pavlova, B. Pezeshkpoor, 2022, Hämostaseologie.

Historical Review on Genetic Analysis in Hemophilia A

J. Oldenburg, A. Pavlova, B. Pezeshkpoor, 2014, Seminars in Thrombosis & Hemostasis.

F8 genetic analysis strategies when standard approaches fail

J. Oldenburg, O. el-Maarri, A. Pavlova, 2013, Hämostaseologie.

F8 gene: embedded in a region of genomic instability representing a hotspot of complex rearrangements

J. Oldenburg, B. Pezeshkpoor, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Further Evidence That MicroRNAs Can Play a Role in Hemophilia A Disease Manifestation: F8 Gene Downregulation by miR-19b-3p and miR-186-5p

J. Oldenburg, Z. Sauna, C. Atreya, 2020, Frontiers in Cell and Developmental Biology.

Experiences in Routine Genetic Analysis of Hereditary Hemorrhagic, Thrombotic, and Platelet Disorders.

A. Pavlova, B. Pezeshkpoor, J. Oldenburg, 2022, Hamostaseologie.

Evidence of pathogenicity of a mutation in 3′ untranslated region causing mild haemophilia A

J. Oldenburg, O. el-Maarri, K. Czogalla, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

Risk stratification integrating genetic data for factor VIII inhibitor development in patients with severe hemophilia A

C. Königs, P. Dönnes, S. Lacroix-Desmazes, 2019, PloS one.

Investigating potential mechanisms underlying FVIII inhibition in acquired hemophilia A associated with mRNA COVID‐19 vaccines

J. Oldenburg, B. Pezeshkpoor, M. Recher, 2022, Journal of Thrombosis and Haemostasis.

Clinical manifestation of hemophilia A in the absence of mutations in the F8 gene that encodes FVIII: role of microRNAs

J. Oldenburg, Z. Sauna, C. Atreya, 2019, Transfusion.

Combined coagulation factor VIII and factor IX deficiency (CDF8F9) in a patient from Lithuania

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2016, Hämostaseologie.

Fibrinogen Bonn (p. Arg510Cys) in the Aα-Chain Is Associated with High Risk of Venous Thrombosis

V. Ivaškevičius, B. Pezeshkpoor, Dr. Ashis Biswas, 2023, Hämostaseologie.

Identification of a third rearrangement at Xq28 that causes severe hemophilia A as a result of homologous recombination between inverted repeats

J. Oldenburg, O. el-Maarri, S. Rost, 2012, Journal of thrombosis and haemostasis : JTH.