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Enhancing quality and impact of early phase dose-finding clinical trial protocols: SPIRIT Dose-finding Extension (SPIRIT-DEFINE) guidance.
BMJ. 2023 Oct 20;383:e076386. doi: 10.1136/bmj-2023-076386.
BMJ. 2023.
PMID: 37863491
No abstract available.
Enhancing reporting quality and impact of early phase dose-finding clinical trials: CONSORT Dose-finding Extension (CONSORT-DEFINE) guidance.
Yap C, Solovyeva O, de Bono J, Rekowski J, Patel D, Jaki T, Mander A, Evans TRJ, Peck R, Hayward KS, Hopewell S, Ursino M, Rantell KR, Calvert M, Lee S, Kightley A, Ashby D, Chan AW, Garrett-Mayer E, Isaacs JD, Golub R, Kholmanskikh O, Richards D, Boix O, Matcham J, Seymour L, Ivy SP, Marshall LV, Hommais A, Liu R, Tanaka Y, Berlin J, Espinasse A, Dimairo M, Weir CJ.
Yap C, et al. Among authors: hommais a.
BMJ. 2023 Oct 20;383:e076387. doi: 10.1136/bmj-2023-076387.
BMJ. 2023.
PMID: 37863501
Free PMC article.
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[How to improve patients and investigators' information on clinical trials: the example of French registry for clinical trials in oncology].
Pauporté I, Manach E, Bachouche N, Hommais A, Détry S, Legrand-Lane C, Barbare JC.
Pauporté I, et al. Among authors: hommais a.
Bull Cancer. 2008 Dec;95(12):1227-32. doi: 10.1684/bdc.2008.0753.
Bull Cancer. 2008.
PMID: 19091658
Free article.
French.
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Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study.
Eikenboom J, Hilbert L, Ribba AS, Hommais A, Habart D, Messenger S, Al-Buhairan A, Guilliatt A, Lester W, Mazurier C, Meyer D, Fressinaud E, Budde U, Will K, Schneppenheim R, Obser T, Marggraf O, Eckert E, Castaman G, Rodeghiero F, Federici AB, Batlle J, Goudemand J, Ingerslev J, Lethagen S, Hill F, Peake I, Goodeve A.
Eikenboom J, et al. Among authors: hommais a.
J Thromb Haemost. 2009 Aug;7(8):1304-12. doi: 10.1111/j.1538-7836.2009.03486.x. Epub 2009 Jun 30.
J Thromb Haemost. 2009.
PMID: 19566550
Free article.
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Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).
Hommais A, Rayes J, Houllier A, Obert B, Legendre P, Veyradier A, Girma JP, Ribba AS.
Hommais A, et al.
Thromb Haemost. 2007 Sep;98(3):593-9.
Thromb Haemost. 2007.
PMID: 17849048
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Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13.
Rayes J, Hommais A, Legendre P, Tout H, Veyradier A, Obert B, Ribba AS, Girma JP.
Rayes J, et al. Among authors: hommais a.
J Thromb Haemost. 2007 Feb;5(2):321-8. doi: 10.1111/j.1538-7836.2007.02296.x. Epub 2006 Nov 1.
J Thromb Haemost. 2007.
PMID: 17087728
Free article.
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Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease.
Hommais A, Stépanian A, Fressinaud E, Mazurier C, Pouymayou K, Meyer D, Girma JP, Ribba AS.
Hommais A, et al.
Thromb Haemost. 2006 May;95(5):776-81.
Thromb Haemost. 2006.
PMID: 16676067
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Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion.
Hommais A, Stépanian A, Fressinaud E, Mazurier C, Meyer D, Girma JP, Ribba AS.
Hommais A, et al.
J Thromb Haemost. 2006 Jan;4(1):148-57. doi: 10.1111/j.1538-7836.2005.01652.x.
J Thromb Haemost. 2006.
PMID: 16409464
Free article.
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