Search Results - "THURET, I"

Biological diagnosis of iron deficiency in children by Thuret, I

“…Measurement of serum ferritin (SF) is currently the laboratory test recommended for diagnosing iron deficiency. In the absence of an associated disease, a low…”
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Gene therapy in beta-thalassemia by Thuret, I

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Current management of thalassemia intermedia by Thuret, I

“…Thalassemia intermedia is a clinical entity where anemia is mild or moderate, requiring no or occasional transfusion. Non-transfusion-dependent thalassemia…”
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Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel by Angelucci, Emanuele, Matthes-Martin, Susanne, Baronciani, Donatella, Bernaudin, Françoise, Bonanomi, Sonia, Cappellini, Maria Domenica, Dalle, Jean-Hugues, Di Bartolomeo, Paolo, de Heredia, Cristina Díaz, Dickerhoff, Roswitha, Giardini, Claudio, Gluckman, Eliane, Hussein, Ayad Achmed, Kamani, Naynesh, Minkov, Milen, Locatelli, Franco, Rocha, Vanderson, Sedlacek, Petr, Smiers, Frans, Thuret, Isabelle, Yaniv, Isaac, Cavazzana, Marina, Peters, Christina

“…Thalassemia major and sickle cell disease are the two most widely disseminated hereditary hemoglobinopathies in the world. The outlook for affected individuals…”
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Health status and quality of life in β-thalassemia adults in Marseille, France by Soubrier, C, Jean, E, De Sainte Marie, B, Agouti, I, Seguier, J, Lavoipierre, V, Clapasson, C, Iline, N, Gonin, J, Giorgi, R, Schleinitz, N, Thuret, I, Badens, C, Bernit, E

“…The life expectancy of β-thalassemia patients has increased over the last 20 years. In this study, we evaluated the current health status and quality of life…”
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Prise en charge actuelle des thalassémies intermédiaires by Thuret, I.

“…Dans les thalassémies dites intermédiaires car l’anémie est moins sévère que dans les formes majeures, les transfusions ne sont pas en règle indiquées ou de…”
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Long-term red blood cell exchange in children with sickle cell disease: Manual or automatic? by Duclos, C, Merlin, E, Paillard, C, Thuret, I, Demeocq, F, Michel, G, Kanold, J

“…Abstract Little information is available on erythrocytapheresis in children with sickle cell disease, and no comparison has ever been made with manual…”
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Health status and quality of life in long-term survivors of childhood leukaemia: the impact of haematopoietic stem cell transplantation by MICHEL, G, BORDIGONI, P, AUQUIER, P, SIMEONI, M.-C, CURTILLET, C, HOXHA, S, ROBITAIL, S, THURET, I, PALL-KONDOLFF, S, CHAMBOST, H, ORBICINI, D

“…We compared late side effects and quality of life (QoL) in 430 survivors of childhood acute leukaemia based on whether they had undergone haematopoietic cell…”
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Lymphocyte-Predominant Hodgkin’s Lymphoma in Children: Therapeutic Abstention After Initial Lymph Node Resection—A Study of the French Society of Pediatric Oncology by PELLEGRINO, B, TERRIER-LACOMBE, M. J, PACQUEMENT, H, VANNIER, J. P, LAMBILLIOTE, C, COUILLAULT, G, BABIN-BOILLETOT, A, THURET, I, DEMEOCQ, F, LEVERGER, G, DELSOL, G, LANDMAN-PARKER, J, OBERLIN, O, LEBLANC, T, PEREL, Y, BERTRAND, Y, BEARD, C, EDAN, C, SCHMITT, C, PLANTAZ, D

“…To clarify treatment strategy for lymphocyte-predominant Hodgkin's lymphoma (LPHL), the French Society of Pediatric Oncology initiated a prospective,…”
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MRI monitoring of myocardial iron overload: Use of cardiac MRI combined with hepatic MRI in a cohort of multi-transfused patients with thalassaemia by Quatre, A, Jacquier, A, Petit, P, Giorgi, R, Thuret, I

“…Abstract Purpose We report the results of combining cardiac and hepatic MRI in the same examination to monitor 48 multi-transfused patients presenting iron…”
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Treatment of childhood acute myeloblastic leukemia: dose intensification improves outcome and maintenance therapy is of no benefit - multicenter studies of the French LAME (Leucémie Aiguë Myéloblastique Enfant) Cooperative Group by Perel, Y, Auvrignon, A, Leblanc, T, Michel, G, Reguerre, Y, Vannier, J-P, Dalle, J-H, Gandemer, V, Schmitt, C, Méchinaud, F, Lejars, O, Piguet, C, Couillaud, G, Pautard, B, Landman-Parker, J, Thuret, I, Aladjidi, N, Baruchel, A, Leverger, G

“…From 1989 to 1998, 341 children were included in the French multicentric LAME (Leucémie Aiguë Myéloblastique Enfant) trials. A total of 309 children were…”
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Height growth during adolescence and final height after haematopoietic SCT for childhood acute leukaemia: the impact of a conditioning regimen with BU or TBI by Bernard, F, Bordigoni, P, Simeoni, M-C, Barlogis, V, Contet, A, Loundou, A, Thuret, I, Leheup, B, Chambost, H, Play, B, Auquier, P, Michel, G

“…We compared the impact of a conditioning regimen with BU ( n =16) or fractionated TBI ( n =42) on height growth during adolescence and final height (FH), in 58…”
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Localized Childhood Hodgkin’s Disease: Response-Adapted Chemotherapy With Etoposide, Bleomycin, Vinblastine, and Prednisone Before Low-Dose Radiation Therapy—Results of the French Society of Pediatric Oncology Study MDH90 by LANDMAN-PARKER, J, PACQUEMENT, H, DONADIEU, J, SCHAISON, G, LEVERGER, G, LEMERLE, J, OBERLIN, O, LEBLANC, T, HABRAND, J. L, TERRIER-LACOMBE, M. J, BERTRAND, Y, PEREL, Y, ROBERT, A, COZE, C, THURET, I

“…The French Society of Pediatric Oncology MDH82 study demonstrated the effectiveness of 20 Gy irradiation of involved fields after doxorubicin, bleomycin,…”
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Multicenter Prospective Study of Children With Sickle Cell Disease: Radiographic and Psychometric Correlation by Bernaudin, F., Verlhac, S., Fréard, F., Roudot-Thoraval, F., Benkerrou, M., Thuret, I., Mardini, R., Vannier, J.P., Ploix, E., Romero, M., Cassé-Perrot, C., Helly, M., Gillard, E., Sebag, G., Kchouk, H., Pracros, J.P., Finck, B., Dacher, J.N., Ickowicz, V., Raybaud, C., Poncet, M., Lesprit, E., Reinert, P.H., Brugières, P.

“…After obtaining familial informed consent, between January 1996 and July 1997, 173 children (5 to 15 years old) with sickle cell disease were enrolled in a…”
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CD34 progenitors are reproducibly recovered in thawed umbilical grafts, and positively influence haematopoietic reconstitution after transplantation by LEMARIE, C, ESTERNI, B, CURTILLET, C, CHABANNON, C, MICHEL, G, CALMELS, B, DAZEY, B, LAPIERRE, V, LECCHI, L, MEYER, A, REA, D, THURET, I, CHAMBOST, H

“…Cord blood (CB) units are increasingly used for allogeneic transplantation. Cell dose, a major factor for CB selection, is evaluated before freezing by each CB…”
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Iron overload of hematological origin: Validation of a screening procedure for cardiac overload by MRI in routine clinical practice by Ernst, O, Thuret, I, Petit, P, Ameur, F, Loundou, A.D, de Kerviler, E, Izzillo, R, Willig, A.L, Pascal, L, Verlhac, S, Mordon, S, Fenaux, P, Rose, C

“…Abstract Purpose Screening for cardiac iron overload is generally done by magnetic resonance imaging (MRI) and demonstrated by a shortening of the myocardial…”
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Late effects of allogeneic bone marrow transplantation for children with acute myeloblastic leukemia in first complete remission: the impact of conditioning regimen without total-body irradiation--a report from the Société Française de Greffe de Moelle by Michel, G, Socié, G, Gebhard, F, Bernaudin, F, Thuret, I, Vannier, J P, Demeocq, F, Leverger, G, Pico, J L, Rubie, H, Mechinaud, F, Reiffers, J, Gratecos, N, Troussard, X, Jouet, J P, Simonin, G, Gluckman, E, Maraninchi, D

“…To evaluate growth, thyroid function, puberty, cardiac function, and the incidence of cataracts in children who received allogeneic bone marrow transplantation…”
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Information for parents of children with sickle cell trait detected by neonatal screening: A 10-year experience by Joly, P, Badens, C, Fekih, S, Philippe, N, Merono, F, Thuret, I, Pondarré, C

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Place de la thérapie génique dans la bêta-thalassémie by Thuret, I.

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Preliminary report of a toxicity study of hydroxyurea in sickle cell disease by de Montalembert, M, Bégué, P, Bernaudin, F, Thuret, I, Bachir, D, Micheau, M

“…AIM To evaluate the tolerance of hydroxyurea in children affected with sickle cell disease. DESIGN Questionnaire study of French physicians likely to treat…”
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