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Items: 16

1.

Performance analysis of the « Blast » flag on ADVIA® 2120/2120i - Results of a multicenter study.

Aidoudi F, Baccini V, Bardet B, Lafon C, Pellicier A, Reins F, Tales P.

Ann Biol Clin (Paris). 2019 Apr 1;77(2):174-178. doi: 10.1684/abc.2019.1423.

PMID:
30998198
2.

A new heterozygous mutation in GP1BA gene responsible for macrothrombocytopenia.

Ghalloussi D, Saut N, Bernot D, Pillois X, Rameau P, Sébahoun G, Alessi MC, Raslova H, Baccini V.

Br J Haematol. 2018 Nov;183(3):503-506. doi: 10.1111/bjh.14986. Epub 2017 Oct 30. No abstract available.

PMID:
29082515
3.

Southeast asian ovalocytosis: the need for a carefull observation of red cell indices and blood smear.

Moulin PA, Nivaggioni V, Saut N, Grosdidier C, Bernot D, Baccini V.

Ann Biol Clin (Paris). 2017 Dec 1;75(6):699-702. doi: 10.1684/abc.2017.1291.

PMID:
29043981
4.

Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features.

Saultier P, Vidal L, Canault M, Bernot D, Falaise C, Pouymayou C, Bordet JC, Saut N, Rostan A, Baccini V, Peiretti F, Favier M, Lucca P, Deleuze JF, Olaso R, Boland A, Morange PE, Gachet C, Malergue F, Fauré S, Eckly A, Trégouët DA, Poggi M, Alessi MC.

Haematologica. 2017 Jun;102(6):1006-1016. doi: 10.3324/haematol.2016.153577. Epub 2017 Mar 2.

5.

Parameters of complete blood count do not predict on-treatment platelet reactivity in acute coronary syndrome patients.

Bonello L, Laine M, Baccini V, Frere C.

Thromb Res. 2017 Apr;152:38-40. doi: 10.1016/j.thromres.2017.02.008. Epub 2017 Feb 14. No abstract available.

PMID:
28219844
6.

Incidental finding of 3 Southeast Asian ovalocytosis cases by attentive examination of blood smears.

Moulin PA, Baccini V.

Blood. 2017 Jan 5;129(1):133. doi: 10.1182/blood-2016-07-729855. No abstract available.

7.

Acquired TET2 mutation in one patient with familial platelet disorder with predisposition to AML led to the development of pre-leukaemic clone resulting in T2-ALL and AML-M0.

Manchev VT, Bouzid H, Antony-Debré I, Leite B, Meurice G, Droin N, Prebet T, Costello RT, Vainchenker W, Plo I, Diop M, Macintyre E, Asnafi V, Favier R, Baccini V, Raslova H.

J Cell Mol Med. 2017 Jun;21(6):1237-1242. doi: 10.1111/jcmm.13051. Epub 2016 Dec 20.

8.

Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34+ progenitors.

Poggi M, Canault M, Favier M, Turro E, Saultier P, Ghalloussi D, Baccini V, Vidal L, Mezzapesa A, Chelghoum N, Mohand-Oumoussa B, Falaise C, Favier R, Ouwehand WH, Fiore M, Peiretti F, Morange PE, Saut N, Bernot D, Greinacher A, BioResource N, Nurden AT, Nurden P, Freson K, Trégouët DA, Raslova H, Alessi MC.

Haematologica. 2017 Feb;102(2):282-294. doi: 10.3324/haematol.2016.147694. Epub 2016 Sep 23.

9.

Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.

Latger-Cannard V, Philippe C, Bouquet A, Baccini V, Alessi MC, Ankri A, Bauters A, Bayart S, Cornillet-Lefebvre P, Daliphard S, Mozziconacci MJ, Renneville A, Ballerini P, Leverger G, Sobol H, Jonveaux P, Preudhomme C, Nurden P, Lecompte T, Favier R.

Orphanet J Rare Dis. 2016 Apr 26;11:49. doi: 10.1186/s13023-016-0432-0.

10.

[Diagnosis of inherited thrombocytopenia].

Baccini V, Alessi MC.

Rev Med Interne. 2016 Feb;37(2):117-26. doi: 10.1016/j.revmed.2015.10.346. Epub 2015 Nov 23. Review. French.

PMID:
26617290
11.

MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations.

Antony-Debré I, Bluteau D, Itzykson R, Baccini V, Renneville A, Boehlen F, Morabito M, Droin N, Deswarte C, Chang Y, Leverger G, Solary E, Vainchenker W, Favier R, Raslova H.

Blood. 2012 Sep 27;120(13):2719-22. Epub 2012 Jun 7.

12.

[Severe thrombocytosis and leukocytosis associated with iron deficiency anaemia: a case-report].

Bernard F, Baccini V, Bagneres D, Rossi P, Demoux AL, Bonin-Guillaume S, Frances Y, Granel B.

Rev Med Interne. 2008 Aug;29(8):662-5. doi: 10.1016/j.revmed.2008.01.006. Epub 2008 Mar 4. French.

PMID:
18308430
13.

[Hematological aspects of Gaucher disease].

Costello R, O'Callaghan T, Baccini V, Sébahoun G.

Rev Med Interne. 2007 Oct;28 Suppl 2:S176-9. Review. French.

PMID:
18228684
14.

Use of hematopoietic progenitor cell count on the Sysmex XE-2100 for peripheral blood stem cell harvest monitoring.

Letestu R, Marzac C, Audat F, Belhocine R, Tondeur S, Baccini V, Garçon L, Cortivo LD, Perrot JY, Lefrère F, Valensi F, Ajchenbaum-Cymbalista F.

Leuk Lymphoma. 2007 Jan;48(1):89-96.

PMID:
17327950
15.

Mammalian target of rapamycin (mTOR) regulates both proliferation of megakaryocyte progenitors and late stages of megakaryocyte differentiation.

Raslova H, Baccini V, Loussaief L, Comba B, Larghero J, Debili N, Vainchenker W.

Blood. 2006 Mar 15;107(6):2303-10. Epub 2005 Nov 10.

16.

Role of p21(Cip1/Waf1) in cell-cycle exit of endomitotic megakaryocytes.

Baccini V, Roy L, Vitrat N, Chagraoui H, Sabri S, Le Couedic JP, Debili N, Wendling F, Vainchenker W.

Blood. 2001 Dec 1;98(12):3274-82.

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