Results 251 to 260 of about 52,382 (294)
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Myelodysplastic Syndromes

Hematology, 2002
AbstractThe myelodysplastic syndromes (MDS) are characterized by hemopoietic insufficiency associated with cytopenias leading to serious morbidity plus the additional risk of leukemic transformation. Therapeutic dilemmas exist in MDS because of the disease’s multifactorial pathogenetic features, heterogeneous stages, and the patients’ generally elderly
Peter L, Greenberg   +2 more
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Myelodysplastic Syndrome

Hematology, 2003
AbstractThe last decade has witnessed a multistep evolution in the understanding of the natural history, clinical manifestations, and some of the molecular mechanisms that underlie the ineffective hematopoiesis and leukemic transformation in the myelodysplastic syndrome (MDS).
Mufti, G, List, A F, Gore, S D, Ho, A Y
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Myelodysplastic Syndromes

Acta Haematologica, 1987
The myelodysplastic syndromes (MDS) represent a group of syndromes having in common a defective production of one or more myeloid cell lines. They occur in patients which are more than 50 years old without any sex preponderance. The term MDS is replacing the obsolete and archaic term of 'preleukemia' and/or 'oligoblastic leukemia'.
C, Sultan   +3 more
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Myelodysplastic Syndromes

Pathology Patterns Reviews, 2003
Myelodysplastic syndromes are a group of clonal hematopoietic stem cell disorders in which there is ineffective hematopoiesis. Affected patients are primarily elderly people, but also at risk are certain subsets of patients who have been exposed to antineoplastic chemotherapy and select patients with primary bone marrow failure syndromes such as ...
Phuong L, Nguyen, Yin, Xu, Aminah, Jatoi
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Myelodysplastic syndrome

Current Opinion in Hematology, 1995
Myelodysplastic syndrome continues to present a formidable clinical challenge. Despite considerable effort, no therapy apart from allogeneic bone marrow transplantation has been shown to prolong survival. Lack of effective therapy for myelodysplastic syndrome is of further concern given recent reports on the high incidence of myelodysplastic syndrome ...
R D, Legare, D G, Gilliland
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The Myelodysplastic Syndromes

Expert Opinion on Biological Therapy, 2007
The myelodysplastic syndrome(s) (MDS), bone marrow stem cell malignancies that share pathogenetic overlap with acute myeloid leukemia, are characterized by peripheral blood cytopenias and, in more advanced subtypes, varied degrees of maturation arrest. Premature apoptosis of bone marrow cellular elements contributes to ineffective hematopoiesis, which ...
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Myelodysplastic Syndromes

Annual Review of Medicine, 2010
Myelodysplastic syndromes (MDS) represent a collection of stem cell disorders characterized by impaired hematopoiesis resulting in low peripheral blood counts. The majority of patients with MDS present with symptoms related to anemia; however, bleeding and infection are the most common causes of death.
Bart L, Scott, H Joachim, Deeg
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The myelodysplastic syndromes

Blood Reviews, 1987
The myelodysplastic syndromes constitute a fascinating model for monoclonal premalignant disorders. Haemopoiesis is 'dysplastic' with inefficient maturation of a slowly expanding or sometimes of a stable population, of blood cell precursors. About one third of the patients evolve into acute leukaemia, the result of either a progressive expansion of the
R L, Verwilghen, M A, Boogaerts
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Myelodysplastic Syndrome

The Indian Journal of Pediatrics, 2008
Pediatric myelodysplastic syndrome (MDS), though rare, constitutes a distinct entity quite different from adult MDS. They have unique clinical features, aggressive clinical course with an overall mean survival of only 9.9 months. A pediatric approach to the WHO classification has become necessary since the WHO classification of MDS has failed to ...
V, Tilak   +3 more
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Myelodysplastic Syndrome

International Journal of Hematology, 2005
During the past 15 years, important progress has been made in the understanding of the biology and prognosis of myelodysplastic syndrome (MDS). MDS is a clonal disorder characterized by ineffective hematopoiesis, which can lead to either fatal cytopenias or acute myelogenous leukemia (AML). Risk-adapted treatment strategies were established because of
Shinji, Nakao   +5 more
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