Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Laurine Laget"'
Autor:
Pascal Pedini, Hajer Graiet, Laurine Laget, Lugdivine Filosa, Jade Chatron, Nicem Cherouat, Jacques Chiaroni, Lucas Hubert, Coralie Frassati, Christophe Picard
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-11 (2021)
Abstract Background Non-invasive molecular analysis of cell-free DNA (cfDNA) became a sensitive biomarker for monitoring organ transplantation or for detection of fetal DNA (cffDNA) in noninvasive prenatal test. In this study, we compared the efficie
Externí odkaz:
https://doaj.org/article/c000149eeeb3473da0865306fac580d4
Autor:
Laurine Laget, Caroline Izard, Elisabeth Durieux‐Roussel, Lugdivine Filosa, Pascal Bailly, Stéphane Mazières, Jacques Chiaroni
Publikováno v:
Transfusion
Transfusion, 2022, ⟨10.1111/trf.17132⟩
Transfusion, 2022, ⟨10.1111/trf.17132⟩
The RH system is one of the most polymorphic blood group systems due to the proximity and opposite orientation of RHD and RHCE genes. Numerous alleles are described and can affect Rh protein expression. This complexity is especially evident in popula
Autor:
Pascal, Pedini, Lugdivine, Filosa, Nelly, Bichel, Christophe, Picard, Monique, Silvy, Jacques, Chiaroni, Caroline, Izard, Laurine, Laget, Stéphane, Mazières
Publikováno v:
Genes. 13(6)
Immunohematology laboratories are regularly facing transfusion issues due to serological weaknesses. Altered (partial) RH antigens account for most of them. In some situations
Autor:
Christophe Picard, Coralie Frassati, Laurine Laget, Jacques Chiaroni, Lugdivine Filosa, Nicem Cherouat, Pascal Pedini, Hajer Graiet, Jade Chatron, Lucas Hubert
Publikováno v:
Journal of Translational Medicine
Journal of Translational Medicine, BioMed Central, 2021, 19, pp.15. ⟨10.1186/s12967-020-02671-8⟩
Journal of Translational Medicine, 2021, 19, pp.15. ⟨10.1186/s12967-020-02671-8⟩
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-11 (2021)
Journal of Translational Medicine, BioMed Central, 2021, 19, pp.15. ⟨10.1186/s12967-020-02671-8⟩
Journal of Translational Medicine, 2021, 19, pp.15. ⟨10.1186/s12967-020-02671-8⟩
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-11 (2021)
Background Non-invasive molecular analysis of cell-free DNA (cfDNA) became a sensitive biomarker for monitoring organ transplantation or for detection of fetal DNA (cffDNA) in noninvasive prenatal test. In this study, we compared the efficiencies of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b01bed1a6baf56e120750cdad82e2129
https://hal.archives-ouvertes.fr/hal-03247642/file/s12967-020-02671-8.pdf
https://hal.archives-ouvertes.fr/hal-03247642/file/s12967-020-02671-8.pdf
Publikováno v:
Transfusion Clinique et Biologique. 28:S82
Autor:
Laurine, Laget, Anne, Cortey
Publikováno v:
La Revue du praticien. 68(5)
Immuno-hematological follow up of pregnant women. The goal of immuno-hematological follow-up during pregnancy is to organize maternal transfusion safety and optimal management of fetal and neonatal hemolytic disease, that may result from maternal imm
Publikováno v:
Transfusion
Transfusion, Wiley, 2019, ⟨10.1111/trf.15266⟩
Transfusion, 2019, ⟨10.1111/trf.15266⟩
Transfusion, Wiley, 2019, ⟨10.1111/trf.15266⟩
Transfusion, 2019, ⟨10.1111/trf.15266⟩
International audience; The GloPID-R (Global Research Collaboration for Infectious Disease Preparedness) Chikungunya (CHIKV), O'nyong-nyong (ONNV) and Mayaro virus (MAYV) Working Group is investigating the natural history, epidemiology and medical ma
Autor:
Julia Gouvitsos, Elisabeth Durieux-Roussel, Caroline Izard, Laurine Laget, Jacques Chiaroni, Isabelle Dettori, V. Ferrera-Tourenc
Publikováno v:
Transfusion Clinique et Biologique
Transfusion Clinique et Biologique, 2018, ⟨10.1016/j.tracli.2018.05.001⟩
Transfusion Clinique et Biologique, Elsevier, 2018, ⟨10.1016/j.tracli.2018.05.001⟩
Transfusion Clinique et Biologique, 2018, ⟨10.1016/j.tracli.2018.05.001⟩
Transfusion Clinique et Biologique, Elsevier, 2018, ⟨10.1016/j.tracli.2018.05.001⟩
Objectives For pregnant women, the serologic test results of D antigen will determine the frequency of RBC antibody detection as well as the indication for RhIG prophylaxis. RHD genotyping is the only method that may provide clear guidance on prophyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::becfcd0a8b6d88a02bf50b9ff4464e4a
https://hal.science/hal-01821545
https://hal.science/hal-01821545
Autor:
Caroline Izard, Elisabeth Durieux-Roussel, Isabelle Dettori, Laurine Laget, Julia Gouvitsos, Jacques Chiaroni
Publikováno v:
Transfusion Clinique et Biologique. 26:S55-S56
Nous rapportons le cas d’un anticorps anti-G ayant entraine une transfusion d’un nouveau-ne. L’expression de l’antigene G (RH12) est codee par l’exon 2 des genes RHD et RHCE*C. La RAI d’une patiente de 34 ans se positive durant sa 5e gros
Autor:
Christine Clapasson, Laurine Laget, Elisabeth Durieux-Roussel, Maude Avias, Caroline Izard, Christophe Picard
Publikováno v:
Transfusion Clinique et Biologique. 26:S55
Le syndrome du lymphocyte passager est une complication rare des transplantations d’organe et greffes de cellules souches hematopoietiques au cours de laquelle les lymphocytes B persistants du donneur produisent des anticorps diriges contre un ou p