Fretigny M - Search Results

1

Prednisolone treatment induced temporary factor IX normalization in mild hemophilia B who required an epidural infiltration: A case report.

Carrette M, Feugray G, Chamouni P, Le Cam Duchez V, Fretigny M, Barbay V, Billoir P. Carrette M, et al. Among authors: fretigny m. Transfus Apher Sci. 2019 Aug;58(4):512-514. doi: 10.1016/j.transci.2019.05.009. Epub 2019 Jun 28. Transfus Apher Sci. 2019. PMID: 31272859

2

Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX.

Row C, Chamouni P, Berger C, Lienhart A, Meunier S, Fretigny M, Dalibard V, Viprey M, Chambost H, Barbay V, Bovet J. Row C, et al. Among authors: fretigny m. Haemophilia. 2021 Jul;27(4):e462-e465. doi: 10.1111/hae.14146. Epub 2020 Sep 30. Haemophilia. 2021. PMID: 32996663 No abstract available.

3

Heterozygous large deletion mimicking homozygous substitution in MCFD2 in a patient with combined Factor V and Factor VIII deficiency.

Rezigue H, Chamouni P, Fretigny M, Barbay V, Le Cam-Duchez V, Bobee V, Lanne S, Dumesnil C, Vinciguerra C, Schneider P, Jourdy Y. Rezigue H, et al. Among authors: fretigny m. Haemophilia. 2024 Jul;30(4):1089-1091. doi: 10.1111/hae.15038. Epub 2024 May 19. Haemophilia. 2024. PMID: 38764219 No abstract available.

4

Algorithms using clinical and genetic data (CYP2C9, VKORC1) are relevant to predict warfarin dose in patients with different INR targets.

Le Cam-Duchez V, Frétigny M, Cailleux N, Gandelin C, Lévesque H, Borg JY. Le Cam-Duchez V, et al. Among authors: fretigny m. Thromb Res. 2010 Sep;126(3):e235-7. doi: 10.1016/j.thromres.2010.05.003. Epub 2010 May 31. Thromb Res. 2010. PMID: 20569971 Clinical Trial. No abstract available.

5

[Contribution of genetic analysis in management of hemophilie patients].

Vinciguerra C, Frétigny M, Négrier C. Vinciguerra C, et al. Among authors: fretigny m. Arch Pediatr. 2010 Jun;17(6):620-1. doi: 10.1016/S0929-693X(10)70027-0. Arch Pediatr. 2010. PMID: 20654809 French. No abstract available.

6

Recurrent F8 and F9 gene variants result from a founder effect in two large French haemophilia cohorts.

Lassalle F, Marmontel O, Zawadzki C, Fretigny M, Bouvagnet P, Vinciguerra C. Lassalle F, et al. Among authors: fretigny m. Haemophilia. 2018 Jul;24(4):e213-e221. doi: 10.1111/hae.13480. Epub 2018 Apr 14. Haemophilia. 2018. PMID: 29656491

7

The highly prevalent deletions in F8 intron 13 found in French mild hemophilia A patients result from both founder effect and recurrent de novo events.

Jourdy Y, Frétigny M, Lassalle F, Lillicrap D, Négrier C, Vinciguerra C. Jourdy Y, et al. Among authors: fretigny m. J Thromb Haemost. 2020 May;18(5):1087-1093. doi: 10.1111/jth.14771. Epub 2020 Mar 20. J Thromb Haemost. 2020. PMID: 32073743 Free article.

8

Reccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu Exonization.

Jourdy Y, Janin A, Fretigny M, Lienhart A, Négrier C, Bozon D, Vinciguerra C. Jourdy Y, et al. Among authors: fretigny m. Am J Hum Genet. 2018 Feb 1;102(2):199-206. doi: 10.1016/j.ajhg.2017.12.010. Epub 2018 Jan 18. Am J Hum Genet. 2018. PMID: 29357978 Free PMC article.

9

Identification of new F8 deep intronic variations in patients with haemophilia A.

Dericquebourg A, Jourdy Y, Fretigny M, Lienhart A, Claeyssens S, Ternisien C, Boisseau P, Rohrlich PS, Négrier C, Vinciguerra C. Dericquebourg A, et al. Among authors: fretigny m. Haemophilia. 2020 Sep;26(5):847-854. doi: 10.1111/hae.14134. Epub 2020 Aug 18. Haemophilia. 2020. PMID: 32812322

10

Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements.

Trossaert M, Lienhart A, Nougier C, Fretigny M, Sigaud M, Meunier S, Fouassier M, Ternisien C, Negrier C, Dargaud Y. Trossaert M, et al. Among authors: fretigny m. Haemophilia. 2014 Jul;20(4):550-8. doi: 10.1111/hae.12381. Epub 2014 Feb 12. Haemophilia. 2014. PMID: 24517184

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