Fiore M - Search Results

1

Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort.

Nurden AT, Pillois X, Fiore M, Alessi MC, Bonduel M, Dreyfus M, Goudemand J, Gruel Y, Benabdallah-Guerida S, Latger-Cannard V, Négrier C, Nugent D, Oiron RD, Rand ML, Sié P, Trossaert M, Alberio L, Martins N, Sirvain-Trukniewicz P, Couloux A, Canault M, Fronthroth JP, Fretigny M, Nurden P, Heilig R, Vinciguerra C. Nurden AT, et al. Among authors: fiore m. Hum Mutat. 2015 May;36(5):548-61. doi: 10.1002/humu.22776. Hum Mutat. 2015. PMID: 25728920 Free article.

2

Genetic testing in the diagnostic evaluation of inherited platelet disorders.

Nurden AT, Fiore M, Pillois X, Nurden P. Nurden AT, et al. Among authors: fiore m. Semin Thromb Hemost. 2009 Mar;35(2):204-12. doi: 10.1055/s-0029-1220328. Epub 2009 Apr 30. Semin Thromb Hemost. 2009. PMID: 19408193 Review.

3

An acquired inhibitor to the GPVI platelet collagen receptor in a patient with lupus nephritis.

Nurden P, Tandon N, Takizawa H, Couzi L, Morel D, Fiore M, Pillois X, Loyau S, Jandrot-Perrus M, Nurden AT. Nurden P, et al. Among authors: fiore m. J Thromb Haemost. 2009 Sep;7(9):1541-9. doi: 10.1111/j.1538-7836.2009.03537.x. Epub 2009 Jul 6. J Thromb Haemost. 2009. PMID: 19583823 Free article.

4

A unique combination of inhibitory and partially activating mutations in beta3 of a patient with variant-type Glanzmann thrombasthenia.

Nurden AT, Fernandes H, Fiore M, Nurden P, Vinciguerra C, Martins N, Sirvain-Trukniewicz P, Couloux A, Heilig R, Pillois X. Nurden AT, et al. Among authors: fiore m. Platelets. 2010;21(6):498-500. doi: 10.3109/09537101003771528. Platelets. 2010. PMID: 20438394 No abstract available.

5

Mutation analysis for a patient with Glanzmann thrombasthenia who produced a landmark isoantibody to the αIIbβ3 integrin.

Nurden AT, Kunicki T, Nurden P, Fiore M, Martins N, Heilig R, Pillois X. Nurden AT, et al. Among authors: fiore m. J Thromb Haemost. 2010 Aug;8(8):1866-8. doi: 10.1111/j.1538-7836.2010.03920.x. Epub 2010 May 21. J Thromb Haemost. 2010. PMID: 20492470 Free article. No abstract available.

6

Rapid diagnosis of the French gypsy mutation in Glanzmann thrombasthenia using high-resolution melting analysis.

Fiore M, Nurden AT, Vinciguerra C, Nurden P, Pillois X. Fiore M, et al. Thromb Haemost. 2010 Nov;104(5):1076-7. doi: 10.1160/TH10-05-0268. Epub 2010 Sep 30. Thromb Haemost. 2010. PMID: 20886184 No abstract available.

7

Founder effect and estimation of the age of the French Gypsy mutation associated with Glanzmann thrombasthenia in Manouche families.

Fiore M, Pillois X, Nurden P, Nurden AT, Austerlitz F. Fiore M, et al. Eur J Hum Genet. 2011 Sep;19(9):981-7. doi: 10.1038/ejhg.2011.61. Epub 2011 Apr 13. Eur J Hum Genet. 2011. PMID: 21487445 Free PMC article.

8

Are bone defects in rare patients with Glanzmann's thrombasthenia associated with ITGB3 or ITGA2B mutations?

Nurden AT, Fiore M, Nurden P, Heilig R, Pillois X. Nurden AT, et al. Among authors: fiore m. Platelets. 2011;22(7):547-51. doi: 10.3109/09537104.2011.573600. Epub 2011 May 11. Platelets. 2011. PMID: 21557682 Review.

9

Glanzmann thrombasthenia: a review of ITGA2B and ITGB3 defects with emphasis on variants, phenotypic variability, and mouse models.

Nurden AT, Fiore M, Nurden P, Pillois X. Nurden AT, et al. Among authors: fiore m. Blood. 2011 Dec 1;118(23):5996-6005. doi: 10.1182/blood-2011-07-365635. Epub 2011 Sep 13. Blood. 2011. PMID: 21917754 Free article. Review.

10

Glanzmann thrombasthenia-like syndromes associated with Macrothrombocytopenias and mutations in the genes encoding the αIIbβ3 integrin.

Nurden AT, Pillois X, Fiore M, Heilig R, Nurden P. Nurden AT, et al. Among authors: fiore m. Semin Thromb Hemost. 2011 Sep;37(6):698-706. doi: 10.1055/s-0031-1291380. Epub 2011 Nov 18. Semin Thromb Hemost. 2011. PMID: 22102273 Review.

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