Search Results - "Pondarré, C."

Effect of hydroxyurea exposure before puberty on sperm parameters in males with sickle cell disease by Joseph, L., Jean, C., Manceau, S., Chalas, C., Arnaud, C., Kamdem, A., Pondarré, C., Habibi, A., Bernaudin, F., Allali, S., de Montalembert, M., Boutonnat-Faucher, B., Arlet, J.-B., Koehl, B., Cavazzana, M., Ribeil, J.-A., Lionnet, F., Berthaut, I., Brousse, V.

“…Sperm parameters are known to be impaired in men with sickle cell disease (SCD). Although treatment with hydroxyurea (HU) has an impact on sperm quality, sperm…”
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Cerebral vasculopathy in children with sickle cell disease: Key issues and the latest data by Corvest, V, Blais, S, Dahmani, B, De Tersant, M, Etienney, A-C, Maroni, A, Ormières, C, Roussel, A, Pondarré, C

“…Cerebral vasculopathy is a common and severe complication of sickle cell disease in children. The pathophysiology consists of progressive damage to the basal…”
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S112: COMPARATIVE SCORE OF HOWELL‐JOLLY BODIES IN SICKLE CELL DISEASE PATIENTS ACCORDING TO GENOTYPE, AGE, SPLENECTOMY OR STEM CELL TRANSPLANTATION HISTORY by Bernaudin, F, Arnaud, C, Kamdem, A, Pondarré, C, Hau, I, Lelong, F, Dalle, J, Peffault de Latour, R, Lezeau, H

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P1469: LONGITUDINAL SICKLE CELL DISEASE COHORT‐STUDY: IN CHILDREN WITH SPLENIC SEQUESTRATION HISTORY OR HYPERSPLENISM, PARTIAL VS TOTAL SPLENECTOMY BEFORE STEM CELL TRANSPLANTATION PRESERVES SPLEEN FUNCTION by Bernaudin, F., Arnaud, C., Kamdem, A., Pondarré, C., Hau, I., Bayani, N., Kuentz, M., Gluckman, E., Peffault de Latour, R., Dhédin, N., Lezeau, H., Dalle, J.‐H.

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CD30+ anaplastic large-cell lymphoma in children : Analysis of 82 patients enrolled in two consecutive studies of the French society of Pediatric Oncology by BRUGIERES, L, LE DELEY, M. C, DELSOL, G, HARTMANN, O, PACQUEMENT, H, MEGUERIAN-BEDOYAN, Z, TERRIER-LACOMBE, M. J, ROBERT, A, PONDARRE, C, LEVERGER, G, DEVALCK, C, RODARY, C

“…The purpose of this study was (1) to investigate the efficacy of chemotherapy regimens designed by the French Society of Pediatric Oncology for childhood…”
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Autoimmune disorders and quadrivalent human papillomavirus vaccination of young female subjects by Grimaldi‐Bensouda, L., Guillemot, D., Godeau, B., Bénichou, J., Lebrun‐Frenay, C., Papeix, C., Labauge, P., Berquin, P., Penfornis, A., Benhamou, P.‐Y., Nicolino, M., Simon, A., Viallard, J.‐F., Costedoat‐Chalumeau, N., Courcoux, M.‐F., Pondarré, C., Hilliquin, P., Chatelus, E., Foltz, V., Guillaume, S., Rossignol, M., Abenhaim, L.

“…Objectives The aim of this study was to investigate whether the quadrivalent human papillomavirus (HPV) vaccine Gardasil is associated with a change in the…”
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Invasive aspergillosis and allogeneic hematopoietic stem cell transplantation in children: a 15-year experience by Crassard, N., Hadden, H., Pondarré, C., Hadden, R., Galambrun, C., Piens, M.A., Pracros, J.P., Souillet, G., Basset, T., Berthier, J.C., Philippe, N., Bertrand, Y.

“…: Despite progress in diagnosis and treatment, invasive aspergillosis (IA) remains a principal cause of mortality due to infection after allogeneic…”
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Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia by Thompson, Alexis A, Walters, Mark C, Kwiatkowski, Janet, Rasko, John E.J, Ribeil, Jean-Antoine, Hongeng, Suradej, Magrin, Elisa, Schiller, Gary J, Payen, Emmanuel, Semeraro, Michaela, Moshous, Despina, Lefrere, Francois, Puy, Hervé, Bourget, Philippe, Magnani, Alessandra, Caccavelli, Laure, Diana, Jean-Sébastien, Suarez, Felipe, Monpoux, Fabrice, Brousse, Valentine, Poirot, Catherine, Brouzes, Chantal, Meritet, Jean-François, Pondarré, Corinne, Beuzard, Yves, Chrétien, Stany, Lefebvre, Thibaud, Teachey, David T, Anurathapan, Usanarat, Ho, P. Joy, von Kalle, Christof, Kletzel, Morris, Vichinsky, Elliott, Soni, Sandeep, Veres, Gabor, Negre, Olivier, Ross, Robert W, Davidson, David, Petrusich, Alexandria, Sandler, Laura, Asmal, Mohammed, Hermine, Olivier, De Montalembert, Mariane, Hacein-Bey-Abina, Salima, Blanche, Stéphane, Leboulch, Philippe, Cavazzana, Marina

“…Gene therapy with CD34+ cells transduced with a lentivirus vector carrying a β-globin gene was performed in 22 patients. At a median of 26 months, all the…”
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Low incidence of sepsis due to viridans streptococci in a ten-year retrospective study of pediatric acute myeloid leukemia by Brunet, A.S., Ploton, C., Galambrun, C., Pondarré, C., Pages, M.P., Bleyzac, N., Freydière, A.M., Barbé, G., Bertrand, Y.

“…Background Infections remain an important cause of morbidity and mortality in children with acute myeloid leukemia (AML), and particularly viridans group…”
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Assessing acute toxicity profiles of HLA‐identical hematopoietic stem cell transplantation in pediatric patients with sickle cell anemia: A comprehensive analysis on behalf of the SFGM‐TC by Delafoy, M., Dalle, J. H., Pondarre, C., Andrieu, G. P., Fahd, M., Yakouben, K., Castelle, M., Koehl, B., Neven, B., Grain, A.

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DNA-Topoisomerase I, a new target for the treatment of neuroblastoma by Vassal, G, Pondarré, C, Cappelli, C, Terrier-Lacombe, M.J, Boland, I, Morizet, J, Bénard, J, Vénuat, A.M, Ardouin, P, Hartmann, O, Gouyette, A

“…DNA-topoisomerase I is the nuclear target of new anticancer drugs, namely camptothecin and its derivatives. In order to establish the rational basis for their…”
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Epstein-Barr virus-related lymphoproliferative disease complicating childhood acute lymphoblastic leukemia : no recurrence after unrelated donor bone marrow transplantation by PONDARRE, C, KEBAILI, K, DIJOUD, F, BASSET, T, PHILIPPE, N, BERTRAND, Y

“…A 16-year-old boy in complete remission of ALL, undergoing oral maintenance therapy, developed intestinal perforation related to EBV-associated…”
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Impact of a paediatric-adult care transition programme on the health status of patients with sickle cell disease: study protocol for a randomised controlled trial (the DREPADO trial) by Hoegy, Delphine, Bleyzac, Nathalie, Gauthier-Vasserot, Alexandra, Cannas, Giovanna, Denis, Angélique, Hot, Arnaud, Bertrand, Yves, Occelli, Pauline, Touzet, Sandrine, Dussart, Claude, Janoly-Dumenil, Audrey

“…Thanks to advancements in medical care, a majority of patients with sickle cell disease (SCD) worldwide live beyond 18 years of age, and therefore, patients…”
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Outcome of unrelated bone marrow donor searches in 174 children resulting in 45 patients transplanted in the HLA-matched and -mismatched situation by SOUILLET, G, REY, S, PHILIPPE, N, GEBUHRER, L, BERTRAND, Y, PUJOL, M, PONDARRE, C, BOURGEOT, J. P, RABA, M, ELJAAFARI, A, CHAPUIS, F, MANEL, A. M

“…The aim of the study was to evaluate the outcome of unrelated bone marrow donor (UBMD) searches initiated for 174 children between 1986 and 1997. Seven…”
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Lupus nephritis in a child with AIDS by Mialou, V, Bertrand, Y, Bouvier, R, Nochy, D, Fabien, N, Nicoud, P, Pondarré, C, Meunier, S, Philippe, N, Cochat, P

“…Concomitant acquired immunodeficiency syndrome (AIDS) and lupus nephritis is an exceptional feature in white patients. A white boy with maternofetal human…”
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Serum procalcitonin rise is only slight in two cases of disseminated aspergillosis by BEAUNE, G, BIENVENU, F, PONDARRE, C, MONNERET, G, BIENVENU, J, SOUILLET, G

“…High serum concentrations of procalcitonin (PCT) have been found during bacterial and parasitic infections. This is a report of two cases of disseminated…”
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Preclinical development of camptothecin derivatives and clinical trials in pediatric oncology by Vassal, G., Pondarré, C., Boland, I., Cappelli, C., Santos, A., Thomas, C., Lucchi, E., Imadalou, K., Pein, F., Morizet, J., Gouyette, A.

“…Although the prognosis of childhood cancers has dramatically improved over the last three decades, new active drugs are needed. Camptothecins represent a very…”
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Renal carcinoma in a patient with glycogen storage disease Ib receiving long-term granulocyte colony-stimulating factor therapy by Donadieu, J, Barkaoui, M, Bézard, F, Bertrand, Y, Pondarré, C, Guibaud, P

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Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia by KANNENGIESSER, Caroline, SANCHEZ, Mayka, LASCAUX, Axelle, PONDARRE, Corinne, SEVILLA NAVARRO, Julian, VIDYATILAKE, Sudharma, BEAUMONT, Carole, GRANDCHAMP, Bernard, MAY, Alison, SWEENEY, Marion, HETET, Gilles, KERR, Briedgeen, MORAN, Erica, FUSTER SOLER, Jose L, MALOUM, Karim, MATTHES, Thomas, OUDOT, Caroline

“…Congenital sideroblastic anemias are rare disorders with several genetic causes; they are characterized by erythroblast mitochondrial iron overload, differ…”
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Thrombopénies constitutionnelles : orientation diagnostique by Pondarre, C.

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