Zobrazeno 1 - 10
of 445
pro vyhledávání: '"C Mazurier"'
Publikováno v:
ISBT Science Series. 11:111-117
Transfusion needs are diversely fulfilled globally. Besides, with population ageing, the various problems faced by healthcare systems will become more and more prominent. As a consequence, the current model of blood supply has to be strengthened, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b4302995427e3eb244b8186788c6e20
https://doi.org/10.1111/voxs.12235
https://doi.org/10.1111/voxs.12235
Autor:
L. Douay, C. Mazurier
Publikováno v:
Revue d'Oncologie Hématologie Pédiatrique. 2:141-149
Resume L’accroissement et le vieillissement de la population mondiale conduiront dans les prochaines decennies a une augmentation de l’incidence des pathologies necessitant un support transfusionnel, et parallelement diminueront la proportion de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6da1a5ea2b8ea3e3f1cc8a2c8c7bb11b
https://doi.org/10.1016/j.oncohp.2014.06.001
https://doi.org/10.1016/j.oncohp.2014.06.001
Autor:
C. Mazurier, L. Douay
Publikováno v:
ISBT Science Series. 8:137-141
The present paper reports the various obstacles cleared during the past decade with the view of generating red blood cells in vitro from various sources of stem cells, for transfusion purposes. We also consider the next developments to be performed f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e6338401abd020782764e5bd503851b
https://doi.org/10.1111/voxs.12029
https://doi.org/10.1111/voxs.12029
Autor:
L. Douay, C. Mazurier
Publikováno v:
Transfusion Clinique et Biologique. 20:90-94
In vitro generation of red blood cells (RBC) makes sense in a context of recurrent shortage. It could be an interesting complementary source for "classic" transfusion products by combining the sufficiency of supply, homemade production of a particula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b42a6dfb32bf7f13809bbf220896a363
https://doi.org/10.1016/j.tracli.2013.02.020
https://doi.org/10.1016/j.tracli.2013.02.020
Publikováno v:
Clinical & Laboratory Haematology. 6:193-197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8453a4213fa2cee5475ae81e7a3caa4f
https://doi.org/10.1111/j.1365-2257.1984.tb00543.x
https://doi.org/10.1111/j.1365-2257.1984.tb00543.x
Publikováno v:
Journal of stem cellsregenerative medicine. 6(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a8ddc09115e434301e158a454c5d20b
https://pubmed.ncbi.nlm.nih.gov/24693133
https://pubmed.ncbi.nlm.nih.gov/24693133
Autor:
C. Mazurier, Edith Fressinaud, J. Goudemand, Christine Gaucher, Sylvie Jorieux, Dominique Meyer
Publikováno v:
Blood. 95:3139-3145
We report 2 new mutations identified in 3 patients and characterized by the markedly decreased affinity of von Willebrand factor (vWF) for factor VIII (FVIII). Patients 2 and 3, who have a typical type 2N phenotype, were found to be compound heterozy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae7704a90f80afa9d79eaf21aba2cb43
https://doi.org/10.1182/blood.v95.10.3139
https://doi.org/10.1182/blood.v95.10.3139
Autor:
J. A. Van Mourik, C. Mazurier, Patrick H.N. Celie, S. Jorieux, Koen Mertens, G. Van Stempvoort
Publikováno v:
British Journal of Haematology. 106:792-800
The functional defect caused by substitution of Arg527 (--> Trp) and Arg531 (--> Gly, His) in factor VIII (FVIII), was explored by employing FVIII derived from patient plasma and recombinant FVIII variants. Mutation of these residues is associated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f06b60ae83bda72da7336676cefe37de
https://doi.org/10.1046/j.1365-2141.1999.01590.x
https://doi.org/10.1046/j.1365-2141.1999.01590.x
Publikováno v:
Blood. 92:4663-4670
In type 2N von Willebrand disease (vWD), von Willebrand factor (vWF) is characterized by normal multimeric pattern, normal platelet-dependent function, but a markedly decreased affinity for factor VIII (FVIII). In this report, we describe the case of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6bd027727c3daf01a7177ffd1e018cb
https://doi.org/10.1182/blood.v92.12.4663
https://doi.org/10.1182/blood.v92.12.4663
Autor:
C Mazurier
Publikováno v:
Haemophilia. 4:40-43
The structural and functional studies of the concentrate of von Willebrand factor (vWF) manufactured by LFB have been first performed as part of the preclinical development of this product specially intended for the treatment of von Willebrand diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b6e224214de9707540cb725f4e28f44
https://doi.org/10.1046/j.1365-2516.1998.0040s3040.x
https://doi.org/10.1046/j.1365-2516.1998.0040s3040.x