Zobrazeno 1 - 10
of 416
pro vyhledávání: '"J Besalduch"'
Autor:
Sancho, Juan‐Manuel, Ribera, Josep‐Maria, Oriol, Albert, Hernandez‐Rivas, Jesus‐Maria, Rivas, Concepcion, Bethencourt, Concepcion, Parody, Ricardo, Deben, Guillermo, Bello, Jose‐Luis, Feliu, Evarist
Publikováno v:
Cancer; June 2006, Vol. 106 Issue: 12 p2540-2546, 7p
Autor:
Juan‐Manuel Sancho, Josep‐Maria Ribera, Albert Oriol, Jesus‐Maria Hernandez‐Rivas, Concepcion Rivas, Concepcion Bethencourt, Ricardo Parody, Guillermo Deben, Jose‐Luis Bello, Evarist Feliu
Publikováno v:
Cancer (0008543X); Jun2006, Vol. 106 Issue 12, p2540-2546, 7p
Autor:
P. Lozano-Vilardell, N. Torreguitart-Mirada, R. Lara-Hernandez, A. Galmés, P. Blanes, J. Besalduch
Publikováno v:
Annales de Chirurgie Vasculaire. 24:314-322
Introduction chez certains patients ayant une ischemie critique de membre inferieur (ICMI), il n’existe pas de possibilite de revascularisation. Dans ces cas particuliers, l’angiogenese therapeutique (AT) utilisant une transplantation de progenit
Autor:
L. Fouillard, Achilles Anagnostopoulos, J. Besalduch, Marrow Transplantation, Alan Tyndall, J. Hansz, Tomas Kozak, Ludwig Kappos, Andreas J. Steck, Alberto M. Marmont, Eric Deconinck, F. J. Zuazu Nagore, Bernd Hertenstein, Harry Openshaw, T. Dentamaro, Jakob Passweg, Marco Rabusin, A Fassas, M. Schipperus, Francesc Graus, Federico Papineschi, Riccardo Saccardi, Eva Havrdova, G. L. Mancardi, Enric Carreras, Aristidis Kazis, Ashwin Kashyap, Marco Musso, J. M. Rowe, G. La Nasa, Alois Gratwohl
Publikováno v:
Journal of Neurology. 249:1088-1097
Rationale Phase I/II studies of autologous hematopoietic stem cell transplantation (HSCT) for multiple sclerosis (MS) were initiated, based on results of experimental transplantation in animal models of multiple sclerosis and clinical observations in
Publikováno v:
Journal of Clinical Apheresis. 17:88-92
The current treatment of hereditary hemochromatosis (HH) consists of performing periodic manual whole blood phlebotomies. Erythroapheresis (EPH) is considered to be an alternative procedure if the classic treatment is contra-indicated. A prospective
Autor:
L. Rosiñol, A. Oriol, A.I. Teruel, D. Hernández, M.J. Blanchard, J. de la Rubia, M. Granell, J. Besalduch, L. Palomera, Y. González, M.A. Etxebeste, J. Díaz-Mediavilla, M.T. Hernández, F. de Arriba, N.C. Gutiérrez, M.L. Martín-Ramos, M.T. Cibeira, M.V. Mateos, J. Martínez-López, A. Alegre, J.J. Lahuerta, J. San Miguel, J. Bladé
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 15:e49-e50
Kingdom; Department of Hematopathology, Aalborg University Hospital, Denmark; Clinical Cancer Research Center, Aalborg University Hospital, Denmark and The Department of Clinical Medicine, Aalborg University, Denmark Background: Today’s diagnostic
Autor:
J. Rifà, A. Obrador, J. Santamaria, S. Teuchmann, E. Benito, J.L. Antich, I. Garau, F. X. Bosch, J. Besalduch, J. Bargay
Publikováno v:
European Journal of Cancer. 30:759-764
This study was conducted to evaluate the impact on survival of perioperative blood transfusion in a series of 698 colorectal cancer patients undergoing radical surgery. Patients were identified, and follow-up was carried out by the local population-b
Autor:
Sojakova, Dominika1,2 (AUTHOR) sojd@ikem.cz, Husakova, Jitka1,2 (AUTHOR) hadj@ikem.cz, Fejfarova, Vladimira1 (AUTHOR) vlfe@ikem.cz, Nemcova, Andrea1 (AUTHOR) nema@ikem.cz, Jarosikova, Radka1 (AUTHOR) jaar@ikem.cz, Kopp, Simon1 (AUTHOR) koxs@ikem.cz, Lovasova, Veronika3,4 (AUTHOR) lovv@ikem.cz, Jude, Edward B.5,6 (AUTHOR) edward.jude@tgh.nhs.uk, Dubsky, Michal1,2 (AUTHOR) mids@ikem.cz
Publikováno v:
International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 18, p10184. 16p.
Autor:
Chan, Yee Jher1, Dileep, Dhananjay1, Rothstein, Samuel M.2, Cochran, Eric W.1, Reuel, Nigel F.1,2 reuel@iastate.edu
Publikováno v:
Advanced Science. 8/27/2024, Vol. 11 Issue 32, p1-17. 17p.
Autor:
N Dalla Venezia, Jean Delaunay, A Forissier, J Besalduch, M Aymerich, Nicole Alloisio, JL Vives Corrons, L Denoroy, I. Besson
Publikováno v:
Blood. 82:1661-1665
We present two Spanish children with hereditary elliptopoikilocytosis. The mother displayed a symptomless elliptocytosis. Spectrin maps showed the alpha I/50–46b abnormality in the mother and in the children. The change was more conspicuous in the