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[Transfusion and its specific problems in pediatrics and neonatology].
Pérel Y, Runel C, Huguenin Y, Renesme L, Aladjidi N. Pérel Y, et al. Among authors: huguenin y. Transfus Clin Biol. 2017 Sep;24(3):101-105. doi: 10.1016/j.tracli.2017.05.017. Epub 2017 Jul 11. Transfus Clin Biol. 2017. PMID: 28709844 Review. French.
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.
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.
Ng BG, Sosicka P, Fenaille F, Harroche A, Vuillaumier-Barrot S, Porterfield M, Xia ZJ, Wagner S, Bamshad MJ, Vergnes-Boiteux MC, Cholet S, Dalton S, Dell A, Dupré T, Fiore M, Haslam SM, Huguenin Y, Kumagai T, Kulik M, McGoogan K, Michot C, Nickerson DA, Pascreau T, Borgel D, Raymond K, Warad D; University of Washington Center for Mendelian Genomics (UW-CMG); Flanagan-Steet H, Steet R, Tiemeyer M, Seta N, Bruneel A, Freeze HH. Ng BG, et al. Among authors: huguenin y. Am J Hum Genet. 2021 Jun 3;108(6):1040-1052. doi: 10.1016/j.ajhg.2021.04.013. Epub 2021 May 7. Am J Hum Genet. 2021. PMID: 33964207 Free PMC article.
Quality of life of siblings of adolescents with severe haemophilia (FRATHEMO): An ancillary study to the TRANSHEMO project.
Nguyen NAT, Auquier P, Beltran Anzola A, Harroche A, Huguenin Y, Hochart A, Meunier S, Frotscher B, Nguyen P, Schneider P, Berger C, Lebreton A, Vanderbecken S, De Raucourt E, D'Oiron R, Oudot-Challard C, Baumstarck K, Boucekine M, Tabélé C, Rosso-Delsemme N, Sannié T, Giraud N, Chambost H, Resseguier N; FRATHEMO Study group. Nguyen NAT, et al. Among authors: huguenin y. Haemophilia. 2024 Apr 29. doi: 10.1111/hae.15023. Online ahead of print. Haemophilia. 2024. PMID: 38684456 No abstract available.
Pubertal development of transfusion-dependent thalassemia patients in the era of oral chelation with deferasirox: results from the French registry.
Broccia MV, Vergier J, Benoit A, Huguenin Y, Lambilliotte A, Castex MP, Gourdon S, Ithier G, Kebaili K, Rohrlich P, Pondarre C, Chamouine A, Simon P, Kpati KPA, Allali S, Baron-Joly S, Bayart S, Billaud N, Brousse V, Dumesnil C, Garnier N, Guichard I, Joseph L, Kamdem A, Maitre J, Mathey C, Paillard C, Phulpin A, Renard C, Stoven C, Touati M, Trochu C, Nafissi SM, Badens C, Szepetowski S, Thuret I. Broccia MV, et al. Among authors: huguenin y. Haematologica. 2024 Feb 22. doi: 10.3324/haematol.2023.283610. Online ahead of print. Haematologica. 2024. PMID: 38385265 Free article.
In vitro characterization of rare anti-αIIbβ3 isoantibodies produced by patients with Glanzmann thrombasthenia that severely block fibrinogen binding and generate procoagulant platelets via complement activation.
Lee CSM, Huguenin Y, Pillois X, Moulieras M, Marcy E, Whittaker S, Chen VMY, Fiore M. Lee CSM, et al. Among authors: huguenin y. Res Pract Thromb Haemost. 2023 Nov 4;8(1):102253. doi: 10.1016/j.rpth.2023.102253. eCollection 2024 Jan. Res Pract Thromb Haemost. 2023. PMID: 38268518 Free PMC article.
27 results