Peyvandi F - Search Results

1

Emicizumab prophylaxis in infants with hemophilia A (HAVEN 7): primary analysis of a phase 3b open-label trial.

Pipe SW, Collins P, Dhalluin C, Kenet G, Schmitt C, Buri M, Jiménez-Yuste V, Peyvandi F, Young G, Oldenburg J, Mancuso ME, Kavakli K, Kiialainen A, Deb S, Niggli M, Chang T, Lehle M, Fijnvandraat K. Pipe SW, et al. Among authors: peyvandi f. Blood. 2024 Apr 4;143(14):1355-1364. doi: 10.1182/blood.2023021832. Blood. 2024. PMID: 38127586 Free PMC article. Clinical Trial.

2

Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII.

Peyvandi F, Tuddenham EG, Akhtari AM, Lak M, Mannucci PM. Peyvandi F, et al. Br J Haematol. 1998 Mar;100(4):773-6. doi: 10.1046/j.1365-2141.1998.00620.x. Br J Haematol. 1998. PMID: 9531348 Free article.

3

Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenarians.

Mannucci PM, Mari D, Merati G, Peyvandi F, Tagliabue L, Sacchi E, Taioli E, Sansoni P, Bertolini S, Franceschi C. Mannucci PM, et al. Among authors: peyvandi f. Arterioscler Thromb Vasc Biol. 1997 Apr;17(4):755-9. doi: 10.1161/01.atv.17.4.755. Arterioscler Thromb Vasc Biol. 1997. PMID: 9108791

4

Management of bleeding disorders in adults.

Peyvandi F, Klamroth R, Carcao M, Federici AB, DI Minno G, Jiménez-Yuste V, Rodriguez Merchán EC. Peyvandi F, et al. Haemophilia. 2012 May;18 Suppl 2:24-36. doi: 10.1111/j.1365-2516.2012.02797.x. Haemophilia. 2012. PMID: 22530576 Review.

5

Genetic sequence analysis of inherited bleeding diseases.

Peyvandi F, Kunicki T, Lillicrap D. Peyvandi F, et al. Blood. 2013 Nov 14;122(20):3423-31. doi: 10.1182/blood-2013-05-505511. Epub 2013 Oct 11. Blood. 2013. PMID: 24124085 Free PMC article. Review.

6

Inhibitor development in non-severe haemophilia across Europe.

Fischer K, Iorio A, Lassila R, Peyvandi F, Calizzani G, Gatt A, Lambert T, Windyga J, Gilman EA, Hollingsworth R, Makris M; EUHASS Participants. Fischer K, et al. Among authors: peyvandi f. Thromb Haemost. 2015 Oct;114(4):670-5. doi: 10.1160/TH14-12-1044. Epub 2015 Aug 13. Thromb Haemost. 2015. PMID: 26293381 Free article.

7

A critical appraisal of one-stage and chromogenic assays of factor VIII activity.

Peyvandi F, Oldenburg J, Friedman KD. Peyvandi F, et al. J Thromb Haemost. 2016 Feb;14(2):248-61. doi: 10.1111/jth.13215. Epub 2016 Feb 1. J Thromb Haemost. 2016. PMID: 26663865 Free article. Review.

8

The past and future of haemophilia: diagnosis, treatments, and its complications.

Peyvandi F, Garagiola I, Young G. Peyvandi F, et al. Lancet. 2016 Jul 9;388(10040):187-97. doi: 10.1016/S0140-6736(15)01123-X. Epub 2016 Feb 18. Lancet. 2016. PMID: 26897598 Review.

9

Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients.

Gorski MM, Blighe K, Lotta LA, Pappalardo E, Garagiola I, Mancini I, Mancuso ME, Fasulo MR, Santagostino E, Peyvandi F. Gorski MM, et al. Among authors: peyvandi f. Blood. 2016 Jun 9;127(23):2924-33. doi: 10.1182/blood-2015-12-685735. Epub 2016 Apr 8. Blood. 2016. PMID: 27060170 Free article.

10

A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effect.

Garagiola I, Seregni S, Mortarino M, Mancuso ME, Fasulo MR, Notarangelo LD, Peyvandi F. Garagiola I, et al. Among authors: peyvandi f. Mol Genet Genomic Med. 2015 Dec 14;4(2):152-9. doi: 10.1002/mgg3.189. eCollection 2016 Mar. Mol Genet Genomic Med. 2015. PMID: 27066508 Free PMC article.

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