Zobrazeno 1 - 10
of 658
pro vyhledávání: '"J Elion"'
Autor:
ESR Sandoval, J Milhomens, LB Viana, JS Borges, RA Panepucci, KTM Grilo, CL Prochaska, R Haddad, LE Leite, J Elion, WE Nemer, ACS Pinto, FLS Santos, M Romana, DT Covas, S Kashima
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S95-S96 (2023)
The characterization of beta globin (β-Hbb) gene haplotypes in sickle cell anemia patients continues to be a valuable source of information for understanding the heterogeneity of the clinical manifestations of this disease and for the regional and g
Externí odkaz:
https://doaj.org/article/91d81d6d9e6f4f4e9c6456b7b77ea43f
Publikováno v:
HemaSphere, Vol 6, Pp 14-15 (2022)
Externí odkaz:
https://doaj.org/article/999a2370281a4c17a9d146003da72c75
Autor:
Y. Lamarre, A. Aich, M. Islam, J.M. Scianni, A.C.S. Pinto, A.M.C. Tavassi, J. Elion, W.E. Nemer, R. Saha, S. Kashima, D.T. Covas
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss , Pp 47- (2020)
Externí odkaz:
https://doaj.org/article/c94c857773614807b872a56f0c17ddb7
Autor:
Mohammad Mazharul Islam, Rajib Saha, W.E. Nemer, A.M.C. Tavassi, Anupam Aich, J. Elion, J.M. Scianni, Yann Lamarre, Simone Kashima, A.C.S. Pinto, Dimas Tadeu Covas
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss, Pp 47-(2020)
Autor:
Evandra Strazza Rodrigues, Simone Kashima, Dimas Tadeu Covas, A.C.S. Pinto, Yann Lamarre, J.S. Borges, M. Romana, L.B. Viana, J. Elion, J.L. Milhomens
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss, Pp 6-7 (2020)
Autor:
J.-J. Cabaud, V. Lovi, Olivier Garraud, J. Ceccaldi, Syria Laperche, J. Elion, J.-P. Vernant, Dominique Bordessoule, I. Pipien, Jean-Daniel Tissot, Christian Hervé, M. Monsellier, J. Hippocrate, B. Clavier, Jean-Baptiste Thibert, Y. Adjibi, M.-F. Mamzer
Publikováno v:
Ethics, Medicine and Public Health. 12:100423
Resume Un des principaux changements de paradigmes introduits par les lois sur les droits des malades depuis 2002 est la primaute du principe d’autonomie de la personne, et de facon consecutive, la recherche d’un consentement aux soins. L’infor
Publikováno v:
Immuno-analyse & Biologie Spécialisée. 26:267-275
Summary Sickle cell syndromes are generally the consequence of the homozygous sickle mutation or associated in trans with another haemoglobin variant or beta-thalassaemia. We present two cases of atypical sickle cell syndrome identified among sickle
Publikováno v:
EMC - Hématologie. 1:1-15
Resume Parmi les hemoglobinopathies, deux types de pathologie sont a distinguer. Dans les anomalies de structure, une hemoglobine (Hb) « anormale » est presente, entrainant ou non des signes fonctionnels. L'HbS, responsable de la drepanocytose, y a
Autor:
L. Fluckiger, P.H. Beaune, S. Mouly, E. Baumelou, J. Elion, Anne Bisagni, J.F. Deleuze, B. Diquet, François Cambien, Ph. Lechat, Christian Funck-Brentano, M. Cano-Petit, P.Y. Arnoux, Laurent Parmentier, L. Mignot, J.M. Job, Jean-Pierre Boissel, François Alhenc-Gelas, A. Parent de Curzon
Publikováno v:
Therapies. 58:279-282
The topics discussed in this article are concerned with studying genomic polymorphism and identifying new therapeutic targets, the role of genetics in preclinical and clinical drug development, and cultural, regulatory and logistical aspects of the d
Autor:
François Alhenc-Gelas, Laurent Parmentier, Anne Bisagni, P.Y. Arnoux, E. Baumelou, P.H. Beaune, J.P. Boissel, F. Cambien, M. Cano-Petit, J.F. Deleuze, B. Diquet, J. Elion, L. Fluckiger, C. Funck-Brentano, J.M. Job, Ph. Lechat, L. Mignot, S. Mouly, A. Parent de Curzon
Publikováno v:
Therapies. 58:275-278
Les sujets discutes concernent l'etude du polymorphisme du genome et l'identification de nouvelles cibles therapeutiques, la place de la genetique dans le developpement preclinique et clinique des medicaments, et les aspects culturels, reglementaires