Pezeshkpoor B - Search Results

1

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

Hirsiger JR, Martinez M, Tsakiris DA, Cittone MG, Graf L, Oldenburg J, Pezeshkpoor B, Recher M, Mueller J, Gerber B, Berger CT. Hirsiger JR, et al. Among authors: pezeshkpoor b. J Thromb Haemost. 2022 Apr;20(4):1015-1018. doi: 10.1111/jth.15665. Epub 2022 Feb 13. J Thromb Haemost. 2022. PMID: 35108443 Free PMC article. No abstract available.

2

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

Pezeshkpoor B, Rost S, Oldenburg J, El-Maarri O. Pezeshkpoor B, et al. J Thromb Haemost. 2012 Aug;10(8):1600-8. doi: 10.1111/j.1538-7836.2012.04809.x. J Thromb Haemost. 2012. PMID: 22672522 Free article.

3

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

Pezeshkpoor B, Zimmer N, Marquardt N, Nanda I, Haaf T, Budde U, Oldenburg J, El-Maarri O. Pezeshkpoor B, et al. J Thromb Haemost. 2013 Sep;11(9):1679-87. doi: 10.1111/jth.12339. J Thromb Haemost. 2013. PMID: 23809411 Free article.

4

F8 genetic analysis strategies when standard approaches fail.

Pezeshkpoor B, Pavlova A, Oldenburg J, El-Maarri O. Pezeshkpoor B, et al. Hamostaseologie. 2014;34(2):167-73. doi: 10.5482/HAMO-13-08-0043. Epub 2013 Dec 3. Hamostaseologie. 2014. PMID: 24296544 Review.

5

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

Pavlova A, Delev D, Pezeshkpoor B, Müller J, Oldenburg J. Pavlova A, et al. Among authors: pezeshkpoor b. Thromb Haemost. 2014 May 5;111(5):851-61. doi: 10.1160/TH13-08-0690. Epub 2014 Jan 23. Thromb Haemost. 2014. PMID: 24452774

6

Genetic testing in bleeding disorders.

de Brasi C, El-Maarri O, Perry DJ, Oldenburg J, Pezeshkpoor B, Goodeve A. de Brasi C, et al. Among authors: pezeshkpoor b. Haemophilia. 2014 May;20 Suppl 4(0 4):54-8. doi: 10.1111/hae.12409. Haemophilia. 2014. PMID: 24762276 Free PMC article. Review.

7

Historical review on genetic analysis in hemophilia A.

Oldenburg J, Pezeshkpoor B, Pavlova A. Oldenburg J, et al. Among authors: pezeshkpoor b. Semin Thromb Hemost. 2014 Nov;40(8):895-902. doi: 10.1055/s-0034-1395161. Epub 2014 Nov 6. Semin Thromb Hemost. 2014. PMID: 25377322 Review.

8

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

Pezeshkpoor B, Theophilus BDM, Guilliatt AM, Oldenburg J, Williams MD, El-Maarri O. Pezeshkpoor B, et al. Haemophilia. 2015 May;21(3):392-397. doi: 10.1111/hae.12606. Epub 2015 Jan 27. Haemophilia. 2015. PMID: 25622659

9

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

Pezeshkpoor B, Oldenburg J. Pezeshkpoor B, et al. Haemophilia. 2015 Jul;21(4):513-5. doi: 10.1111/hae.12687. Epub 2015 May 4. Haemophilia. 2015. PMID: 25939373 No abstract available.

10

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

Pezeshkpoor B, Castoldi E, Mahler A, Hanel D, Müller J, Hamedani NS, Biswas A, Oldenburg J, Pavlova A. Pezeshkpoor B, et al. J Thromb Haemost. 2016 Jul;14(7):1353-63. doi: 10.1111/jth.13339. Epub 2016 Jun 13. J Thromb Haemost. 2016. PMID: 27090446 Free article.

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