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Primary hemorrhagic stroke in a 12-year-old female with sickle cell disease and normal Transcranial Doppler
Pediatric Hematology and Oncology, 06/23/08
Development and evaluation of a reverse dot blot assay for the simultaneous detection of six common Chinese G6PD mutations and one polymorphism
Blood Cells, Molecules, and Diseases, 06/23/08
Glycophorin A: Band 3 aid
Blood Cells, Molecules, and Diseases, 06/23/08
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Identification of a novel frameshift mutation at codon 53 (T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family
Blood Cells, Molecules, and Diseases, 06/23/08
Non-electrolyte permeability of deoxygenated sickle cells compared
Blood Cells, Molecules, and Diseases, 06/23/08
Presence of cytosolic peroxiredoxin 2 in the erythrocyte membrane of patients with hereditary spherocytosis
Blood Cells, Molecules, and Diseases, 06/23/08
Recessive hereditary methemoglobinemia: Two novel mutations in the NADH-cytochrome b5 reductase gene
Blood Cells, Molecules, and Diseases, 06/23/08
Erythropoietin and granulocyte-colony stimulating factor treatment associated with improved survival in myelodysplastic syndrome
Journal of Clinical Oncology, 06/19/08
HES1 is a novel interactor of the Fanconi anemia core complex
Blood, 06/19/08
Quality of life in patients with transfusion-dependent thalassemia after hematopoietic SCT
Bone Marrow Transplantation, 06/19/08
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Indexed Journals: Journal of Clinical Oncology, Cancer Research, Annals Oncology
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