Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Patrice Richard"'
Autor:
Andrés Fontana, Anthony Delage, Aurélien Périgaud, Patrice Richard, David Carsenat, Guillaume Acikalin, Serge Verdeyme, Barbara Bonnet, Ludovic Carpentier, Nicolas Delhote
Publikováno v:
IEEE Transactions on Microwave Theory and Techniques. :1-14
Autor:
Andres Fontana, Aurelien Perigaud, Nicolas Delhote, David Carsenat, Guillaume Acikalin, Patrice Richard, Stephane Bila
Publikováno v:
2021 IEEE MTT-S International Microwave Filter Workshop (IMFW).
Autor:
Jean Michel Cayuela, Patrice Richard, Agnès Devergie, Eliane Gluckman, Gérard Socié, Philippe Guardiola, Peter Kurre, Patricia Ribaud, Rainer Storb, R. Traineau, Helene Esperou, Amalia Vlad
Publikováno v:
British Journal of Haematology. 122:806-809
Allogeneic transplantation is the only curative treatment for Fanconi anaemia (FA) patients who develop myeloid malignancies. Dose-intensive preparative regimens, to decrease disease recurrence, lead to unacceptable transplant-related toxicity in FA.
Autor:
Patrice Richard, François Leteurtre, Eliane Gluckman, Pauline De La Salmonière, Gwenaelle Le Roux, Maria Helena Noguera, Philippe Guardiola, Marie-Thérèse Daniel, Odile Maarek, Vanderson Rocha, Roland Berger, Xiaxin Li
Publikováno v:
British Journal of Haematology. 120:836-845
Summary. Fanconi's anaemia (FA) is an autosomal recessive disorder characterized by progressive bone marrow failure and a susceptibility to cancer. Haematopoietic stem cell transplantation is the only curative method for restoring normal haematopoies
Autor:
Patrice Richard, E. D. Carosella, F. Leteurtre, Xiaxin Li, G. Le Roux, Eliane Gluckman, Philippe Guardiola, Jean-Christophe Sergere
Publikováno v:
British Journal of Haematology. 105:883-893
Fanconi's anaemia (FA) is an autosomal recessive disorder characterized by progressive bone marrow failure that often evolves towards acute leukaemia. FA also belongs to a group of chromosome instability diseases. Because telomeres are directly invol
Autor:
Patrice Richard, Odile Maarek, Agnès Devergie, Eliane Gluckman, Helene Esperou, Gérard Socié, Gaelle Piel, T. Girinski, Patricia Ribaud, Olivier Brison, Maria-Helena Noguera, Nathalie Parquet
Publikováno v:
British Journal of Haematology. 103:249-255
We describe the long-term follow-up of 50 Fanconi's anaemia patients who were transplanted from a related donor with a median follow-up of >6 years. The survival estimate was 74.4% at 54 months and 58.5% at 100 months. All patients were conditioned w
Autor:
Patrice Richard
Publikováno v:
Tiers-Monde. 33:789-808
Richard Patrice. Analyse de la consommation alimentaire et modèle d'offre. In: Tiers-Monde, tome 33, n°132, 1992. Le fait alimentaire : débats et perspectives, sous la direction de Emmanuel Calvo et Georges Courade. pp. 789-808.
Autor:
Agnès Devergie, Patricia Ribaud, Patrice Richard, Anne Janin, R. Traineau, Philippe Guardiola, Xiaxin Li, Eliane Gluckman, Gérard Socié, Helene Esperou
Publikováno v:
Blood. 103(1)
To assess whether Fanconi anemia (FA) patients might be at risk for acute graft-versus-host disease (AGvHD) despite using low-intensity conditionings, we retrospectively analyzed the incidence of AGvHD and its impact on outcome in 37 FA patients and
Autor:
Xiaxin, Li, François, Leteurtre, Vanderson, Rocha, Philippe, Guardiola, Roland, Berger, Marie-Therese, Daniel, Maria Helena, Noguera, Odile, Maarek, Gwenaëlle L E, Roux, Pauline, de la Salmonière, Patrice, Richard, Eliane, Gluckman
Publikováno v:
British journal of haematology. 120(5)
Fanconi's anaemia (FA) is an autosomal recessive disorder characterized by progressive bone marrow failure and a susceptibility to cancer. Haematopoietic stem cell transplantation is the only curative method for restoring normal haematopoiesis, and s
Publikováno v:
British journal of haematology. 83(4)
Summary. Fanconi's anaemia (FA) is the most common of the constitutional aplastic anaemias; the mechanisms leading to aplasia in this disease are poorly understood. A number of mechanisms have been implicated in the pathogenesis of acquired aplastic