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Major Complications of Regional Anesthesia in France
Monoclonal T-cell expansions in asymptomatic individuals and in patients with large granular leukemia consist of cytotoxic effector T cells expressing the activating CD94:NKG2C/E and NKD2D killer…
We have analyzed the phenotype, cytokine profile, and mitotic history (telomere length) of monoclonal T-cell expansions in 5 CD3(+) T-cell large granular lymphocyte (TLGL) leukemia patients by… Expand
Microangiopathic hemolytic anemia complicating FK506 (tacrolimus) therapy
We describe 3 episodes of microangiopathic hemolytic anemia (MAHA) in 2 solid organ recipients under FK506 (tacrolimus) therapy. In both cases, discontinuation of FK506 and treatment with plasma… Expand
Anémie ferriprive, inflammatoire ou mixte: comment orienter le diagnostic?
The diagnosis of pure iron-deficient anemia or anemia of chronic disease is easy. However, in mixed situations, conventional laboratory tests for iron status are influenced by the inflammatory… Expand
L'anémie du sujet âgé: une pathologie fréquente à ne pas banaliser
Anemia is a frequent disease in elderly persons, but is often undertreated and misunderstood as a physiologic consequence of aging. Nevertheless, its association with some negative clinical impacts… Expand
Increased apoptosis in acquired sideroblastic anaemia
- T. Matthes, G. Meyer, K. Samii, P. Beris
- Biology, Medicine
- British journal of haematology
- 1 December 2000
Idiopathic acquired sideroblastic anaemias (IASAs) form a subgroup of the myelodysplastic syndromes and are characterized by mitochondrial iron accumulation, bone marrow erythroid hyperplasia and… Expand
Central Venous Pressure And Pulmonary Wedge Pressure
Massive delayed hemolysis following peripheral blood stem cell transplantation with minor ABO incompatibility.
After hematopoietic stem cell transplantation, delayed immune hemolysis may occur when donor-derived B lymphocytes carried with the graft produce immune antibodies against the recipient's… Expand
Iron overload in patients with sideroblastic anaemia is not related to the presence of the haemochromatosis Cys282Tyr and His63Asp mutations
Forty Caucasian patients with primary acquired sideroblastic anaemia (SA), were investigated for the presence of the Cys282Tyr and/or His63Asp mutation as possible cofactor(s) for iron overload. One… Expand
Hereditary hyperferritinaemia cataract syndrome: does it exist in Switzerland?
- J. Rosochova, A. Kapetanios, C. Pournaras, L. Vadas, K. Samii, P. Beris
- Schweizerische medizinische Wochenschrift
- 4 March 2000
Recent research in iron metabolism has revealed the existence of iron-responding elements in the 5'UTR of the mRNA of ferritin. Binding of these structures with iron-regulatory proteins regulates… Expand