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Page 1
Microparticle phenotypes are associated with driver mutations and distinct thrombotic risks in essential thrombocythemia.
Haematologica. 2016 Sep;101(9):e365-8. doi: 10.3324/haematol.2016.144279. Epub 2016 May 31.
Haematologica. 2016.
PMID: 27247323
Free PMC article.
No abstract available.
Natural history of patients with congenital dysfibrinogenemia.
Casini A, Blondon M, Lebreton A, Koegel J, Tintillier V, de Maistre E, Gautier P, Biron C, Neerman-Arbez M, de Moerloose P.
Casini A, et al. Among authors: tintillier v.
Blood. 2015 Jan 15;125(3):553-61. doi: 10.1182/blood-2014-06-582866. Epub 2014 Oct 15.
Blood. 2015.
PMID: 25320241
Free PMC article.
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Mutational Epidemiology of Congenital Fibrinogen Disorders.
Casini A, Blondon M, Tintillier V, Goodyer M, Sezgin ME, Gunes AM, Hanss M, de Moerloose P, Neerman-Arbez M.
Casini A, et al. Among authors: tintillier v.
Thromb Haemost. 2018 Nov;118(11):1867-1874. doi: 10.1055/s-0038-1673685. Epub 2018 Oct 17.
Thromb Haemost. 2018.
PMID: 30332696
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Fibrin clot structure in patients with congenital dysfibrinogenaemia.
Casini A, Duval C, Pan X, Tintillier V, Biron-Andreani C, Ariëns RAS.
Casini A, et al. Among authors: tintillier v.
Thromb Res. 2016 Jan;137:189-195. doi: 10.1016/j.thromres.2015.11.008. Epub 2015 Nov 10.
Thromb Res. 2016.
PMID: 26577257
Free article.
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Compliance with Early Long-Term Prophylaxis Guidelines for Severe Hemophilia A.
Saultier P, Guillaume Y, Demiguel V, Berger C, Borel-Derlon A, Claeyssens S, Harroche A, Oudot C, Rafowicz A, Trossaert M, Wibaut B, Vinciguerra C, Boucekine M, Baumstarck K, Meunier S, Calvez T, Chambost H; FranceCoag PUPs / CoMETH Prophylaxis Study Group; Hemophilia Treatment Centers of Paris-Necker.
Saultier P, et al.
J Pediatr. 2021 Jul;234:212-219.e3. doi: 10.1016/j.jpeds.2021.02.071. Epub 2021 Mar 4.
J Pediatr. 2021.
PMID: 33676933
Clinical Trial.
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Colonoscopy in patients with haemophilia: the duration of clotting factor coverage must be adjusted to suit the procedure.
Tintillier V, Branche J, Maunoury V, Goudemand J, Renom P.
Tintillier V, et al.
Haemophilia. 2013 Sep;19(5):e296-8. doi: 10.1111/hae.12174. Epub 2013 May 15.
Haemophilia. 2013.
PMID: 23672809
No abstract available.
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FranceCoag: a 22-year prospective follow-up of the national French cohort of patients with inherited bleeding disorders.
Doncarli A, Demiguel V, Guseva Canu I, Goulet V, Bayart S, Calvez T, Castet S, Dalibard V, Demay Y, Frotscher B, Goudemand J, Lambert T, Milien V, Oudot C, Sannié T, Chambost H; FranceCoag Network.
Doncarli A, et al.
Eur J Epidemiol. 2019 May;34(5):521-532. doi: 10.1007/s10654-018-0468-7. Epub 2018 Dec 5.
Eur J Epidemiol. 2019.
PMID: 30515664
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Analyses of the FranceCoag cohort support differences in immunogenicity among one plasma-derived and two recombinant factor VIII brands in boys with severe hemophilia A.
Calvez T, Chambost H, d'Oiron R, Dalibard V, Demiguel V, Doncarli A, Gruel Y, Huguenin Y, Lutz P, Rothschild C, Vinciguerra C, Goudemand J; for FranceCoag Collaborators.
Calvez T, et al.
Haematologica. 2018 Jan;103(1):179-189. doi: 10.3324/haematol.2017.174706. Epub 2017 Oct 12.
Haematologica. 2018.
PMID: 29025913
Free PMC article.
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