Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Gwenaelle Le Roux"'
Autor:
Fernando O. Pinto, Thierry Leblanc, Delphine Chamousset, Gwenaelle Le Roux, Benoit Brethon, Bruno Cassinat, Jérôme Larghero, Jean-Pierre de Villartay, Dominique Stoppa-Lyonnet, André Baruchel, Gérard Socié, Eliane Gluckman, Jean Soulier
Publikováno v:
Haematologica, Vol 94, Iss 4 (2009)
Background Patients with bone marrow failure and undiagnosed underlying Fanconi anemia may experience major toxicity if given standard-dose conditioning regimens for hematopoietic stem cell transplant. Due to clinical variability and/or potential eme
Externí odkaz:
https://doaj.org/article/99fc0290295643a597fd4104449471a0
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:
André Baruchel, Thierry Leblanc, Gwenaelle Le Roux, Benoit Brethon, Delphine Chamousset, Fernando O. Pinto, Jean-Pierre de Villartay, Jean Soulier, Dominique Stoppa-Lyonnet, Gérard Socié, Jérôme Larghero, Bruno Cassinat, Eliane Gluckman
Publikováno v:
Haematologica. 94(4)
Background Patients with bone marrow failure and undiagnosed underlying Fanconi anemia may experience major toxicity if given standard-dose conditioning regimens for hematopoietic stem cell transplant. Due to clinical variability and/or potential eme
Autor:
Thierry Leblanc, Gwenaelle Le Roux, Benoit Brethon, Jérôme Larghero, Eliane Gluckman, André Baruchel, Bruno Cassinat, Fernando O. Pinto, Caroline Oudot, Jean Soulier, Odile Maarek, Gérard Socié, Moema Santos
Publikováno v:
Blood. 108:991-991
The Bone Marrow Failure (BMF) syndromes comprise a variety of distinct acquired or inherited clinical entities. Early distinction between syndromes has clear implications in the disease management and outcome. Fanconi anemia (FA), the most frequent c
Autor:
Gérard Socié, Moema Santos, Vanderson Rocha, Jean Soulier, Eliane Gluckman, André Baruchel, Helene Esperou, Thierry Leblanc, Jérôme Larghero, Hélène Dastot, Fernando O. Pinto, Gwenaelle Le Roux
Publikováno v:
Blood. 106:1056-1056
Early diagnosis of Fanconi Anemia (FA) in patients with bone marrow failure is critical for optimal clinical management. However, the remarkably high clinical variability and the potential emergence of revertant hematopoietic cells (somatic mosaicism