Search Results - "Beris, P."

Detection, evaluation, and management of preoperative anaemia in the elective orthopaedic surgical patient: NATA guidelines by Goodnough, L.T., Maniatis, A, Earnshaw, P, Benoni, G, Beris, P, Bisbe, E, Fergusson, D.A., Gombotz, H, Habler, O, Monk, T.G., Ozier, Y, Slappendel, R, Szpalski, M

“…Previously undiagnosed anaemia is common in elective orthopaedic surgical patients and is associated with increased likelihood of blood transfusion and…”
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Perioperative anaemia management: consensus statement on the role of intravenous iron by Beris, P., Muñoz, M., García-Erce, J.A., Thomas, D., Maniatis, A., Van der Linden, P.

“…A multidisciplinary panel of physicians was convened by Network for Advancement of Transfusion Alternatives to review the evidence on the efficacy and safety…”
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Zinc-induced copper deficiency in Wilson disease by Horvath, J, Beris, P, Giostra, E, Martin, P-Y, Burkhard, P R

“…Neurological manifestations of copper deficiency typically involve a myelopathy resembling subacute combined degeneration, yet optic and peripheral…”
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Atypical presentation of acute myeloid leukemia: cardiac myeloid sarcoma by Rigamonti, Fabio, Beris, P., Sanchez-Pareja, A., Meyer, P., Ashrafpoor, G., Zaza, S., Passweg, J., Chalandon, Y.

“…We present the case of a 52-year-old man with a 2-month history of dyspnea, bilateral pleural effusion and cardiomegaly of rapid onset. A cardiac ultrasound…”
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Lentiviral PU.1 overexpression restores differentiation in myeloid leukemic blasts by DURUAL, S, RIDEAU, A, RUAULT-JUNGBLUT, S, COSSALI, D, BERIS, P, PIGUET, V, MATTHES, T

“…PU.1, a transcription factor of the ETS family, plays a pivotal role in normal hematopoiesis, and particularly in myeloid differentiation. Altered PU.1…”
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Introduction: management of thalassemia by Beris, P

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Iron overload in patients with sideroblastic anaemia is not related to the presence of the haemochromatosis Cys282Tyr and His63Asp mutations by Beris, P., Samii, K., Darbellay, R., Zoumbos, N., Tsoplou, P., Kourakli, A., Preud'Homme, C., Fenaux, P.

“…Forty Caucasian patients with primary acquired sideroblastic anaemia (SA), were investigated for the presence of the Cys282Tyr and/or His63Asp mutation as…”
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Epoetin alfa: new directions in orthopedic surgery by Beris, P

“…The introduction of autologous blood (AB) donation programs has led to a decrease in the number of orthopedic surgery patients exposed to allogeneic blood,…”
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Optimized lentiviral transduction of erythroid precursors from healthy adults and patients with myelodysplastic syndromes by MATTHES, T. W, KINDLER, V, LEUBA, F, FRENCH, L. E, CHAPUIS, B, BERIS, P, PIGUET, V

“…Lentivectors, derived from human immunodeficiency virus-1 (HIV-1), represent a novel investigational and therapeutic tool for targeting hematopoietic…”
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Recombinant human erythropoietin as adjuvant treatment for autologous blood donation in elective surgery with large blood needs (> or=5 units): a randomized study by De Pree, Christian, Mermillod, Bernadette, Hoffmeyer, Pierre, Beris, Photis

“…BACKGROUND: Autologous blood transfusion presents no infectious or immunologic side effects. The aim of this randomized study was to determine the impact of…”
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Adoptive immunotherapy for recurrent CML after BMT by Helg, C, Roux, E, Beris, P, Cabrol, C, Wacker, P, Darbellay, R, Wyss, M, Jeannet, M, Chapuis, B, Roosnek, E

“…Three patients with CML who relapsed after transplantation with T-depleted BM from their HLA-identical siblings were treated with transfusions of donor…”
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Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease by Longo, L, Bessler, M, Beris, P, Swirsky, D, Luzzatto, L

“…Paroxysmal nocturnal haemoglobinuria (PNH) is an acquired haemolytic anaemia, clonal in nature, due to somatic mutation. PNH may evolve to aplastic anaemia;…”
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Epoetin alfa as an adjuvant to autologous blood donation by Beris, P

“…The development of anemia is one factor that can limit the donation of sufficient autologous blood (AB) to meet a patient's expected blood requirements…”
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Spurious Extreme Reticulocytosis with an Automated Reticulocyte Analyzer by Laurencet, France M, Martinez, Thelmo, Beris, Photis

“…To the Editor: Automated reticulocyte analysis is based on flow-cytometric techniques and the Sysmex R series of instruments for quantification of erythrocyte…”
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Prevention of beta-thalassemia major and Hb Bart's hydrops fetalis syndrome by Beris, P, Darbellay, R, Extermann, P

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Deferasirox in iron-overloaded patients with transfusion-dependent myelodysplastic syndromes: Results from the large 1-year EPIC study by Gattermann, Norbert, Finelli, Carlo, Porta, Matteo Della, Fenaux, Pierre, Ganser, Arnold, Guerci-Bresler, Agnes, Schmid, Mathias, Taylor, Kerry, Vassilieff, Dominique, Habr, Dany, Domokos, Gabor, Roubert, Bernard, Rose, Christian

“…Abstract The prospective 1-year EPIC study enrolled 341 patients with myelodysplastic syndromes (MDS); although baseline iron burden was >2500 ng/mL, ∼50% were…”
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Thalidomide in patients with advanced multiple myeloma by Yakoub-Agha, I, Moreau, P, Leyvraz, S, Berthou, C, Payen, C, Dumontet, C, Grosbois, B, Beris, P, Duguet, C, Attal, M, Harousseau, J L, Facon, T

“…Recently, a report has suggested the efficacy and safety of thalidomide in refractory multiple myeloma. In an attempt to assess the efficacy and tolerance of…”
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Pseudoreticulocytosis in a case of myelodysplastic syndrome with translocation t(1;14) (q42;q32) by de Pree, C, Cabrol, C, Frossard, J L, Beris, P

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HEREDITARY XEROCYTOSIS: CLINICAL AND BIOLOGICAL PRESENTATION AT DIAGNOSIS IN A RETROSPECTIVE SERIES OF 103 PATIENTS by Picard, V., Guitton, C., Lahary, A., Martinez, P. Aguilar, Ruivard, M., Rose, C., Perrin, J., Barro, C., Lifermann, F., Jaureguiberry, J. -P. De, Deconinck, E., Beneteau, C., Lefebvre, T., Toutain, F., Le Coz, M. -F., Berger, C., Proulle, V., Beris, P., Godeau, B., Very, C., Garcon, Loic

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Etoposide and secondary haematological malignancies: coincidence or causality? by Zulian, G B, Jotterand Bellomo, M, Cabrol, C, Beris, P, Mermillod, B, Alberto, P

“…Secondary haematological malignancies (SHM) induced by alkylating agents show cytogenetic abnormalities involving mainly chromosomes 5 and 7. Etoposide and…”
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