The PI-3kinase pathway in hematopoietic stem cells and leukemia-initiating cells: A mechanistic difference between normal and cancer stem cells Fulltext Access 4 Pages 2008
Antibodies to oxidized LDL/β2-glycoprotein I in antiphospholipid syndrome patients with venous and arterial thromboembolism Fulltext Access 4 Pages 2008
Antiphospholipid antibodies in a family with dehydrated hereditary stomatocytosis Fulltext Access 4 Pages 2008
Is there evidence for persistent or transient positive lupus anticoagulants according to the degree of prolongation of clotting tests? Fulltext Access 4 Pages 2008
Prevalence of pyruvate kinase deficiency among the south Iranian population: Quantitative assay and molecular analysis Fulltext Access 4 Pages 2008
Distribution of CYP1A1⁎2A polymorphism in adult patients with acute lymphoblastic leukemia in a Mexican population Fulltext Access 4 Pages 2008
Protein disulfide isomerase as a trigger for tissue factor-dependent fibrin generation Fulltext Access 4 Pages 2008
Increased von Willebrand factor antigen and high molecular weight multimers in sickle cell disease associated with nocturnal hypoxemia Fulltext Access 4 Pages 2008
Identification of a novel frameshift mutation at codon 53 (−T) in the β-globin gene causing dominantly inherited β-thalassemia in a Chinese Miao family Fulltext Access 4 Pages 2008
Using microfluidics to understand the effect of spatial distribution of tissue factor on blood coagulation Fulltext Access 4 Pages 2008
Genetic defects in von Willebrand disease type 3 in Indian and Greek patients Fulltext Access 4 Pages 2008
Immunoglobulin kappa gene repertoire and somatic hypermutation patterns in follicular lymphoma Fulltext Access 4 Pages 2008
p15Ink4b: Dual function in myelopoiesis and inactivation in myeloid disease Fulltext Access 4 Pages 2008
The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency Fulltext Access 4 Pages 2008
Association between thrombosis and bloodstream infection in neonates with peripherally inserted catheters Fulltext Access 4 Pages 2008
Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia Fulltext Access 4 Pages 2008
A 10376 bp deletion of FECH gene responsible for erythropoietic protoporphyria Fulltext Access 4 Pages 2008
Statins and inflammation: Reciprocal effectors to endothelial progenitors? Fulltext Access 4 Pages 2008
Immunogenetic factors in donors and patients that affect the outcome of hematopoietic stem cell transplantation Fulltext Access 4 Pages 2008
Enhancing T cell reconstitution after hematopoietic stem cell transplantation: A brief update of the latest trends Fulltext Access 4 Pages 2008
Phase 1 study of human plasma-derived plasmin (TAL-05-00018) in hemodialysis graft occlusion Fulltext Access 4 Pages 2008
Low-molecular-weight heparin use in the obese, elderly, and in renal insufficiency Fulltext Access 4 Pages 2008
Oral anticoagulant therapy for patients with atrial fibrillation - an update Fulltext Access 4 Pages 2008
WT1-specific T cell receptor gene therapy: Improving TCR function in transduced T cells Fulltext Access 4 Pages 2008
Preventing and managing bleeding complications in anticoagulated patients: A case based approach Fulltext Access 4 Pages 2008
Prevalence of pre-stroke low bone mineral density and vertebral fracture in first stroke patients Fulltext Access 4 Pages 2008
Estrogen and bone: Insights from estrogen-resistant, aromatase-deficient, and normal men Fulltext Access 4 Pages 2008
Budd-Chiari syndrome in a young female with factor V Leiden mutation: Successful treatment with lepirudin, a direct thrombin inhibitor Fulltext Access 4 Pages 2008
Warfarin-reversal: results of a phase III study with pasteurised, nanofiltrated prothrombin complex concentrate Fulltext Access 4 Pages 2008
Two strategies of clopidogrel loading dose to decrease the frequency of clopidogrel resistance in patients undergoing percutaneous coronary intervention Fulltext Access 4 Pages 2008
Relationship between small-for-gestational age births and maternal thrombophilic mutations Fulltext Access 4 Pages 2008
Epidural hematoma following tissue plasminogen activator (tPA) therapy for pulmonary embolism in a pediatric patient with stage IV Burkitt's lymphoma: A case report Fulltext Access 4 Pages 2008
CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men Fulltext Access 4 Pages 2008
Low serum levels of prohepcidin, but not hepcidin-25, are related to anemia in familial amyloidosis TTR V30M Fulltext Access 4 Pages 2008
The role of smooth muscle derived tissue factor in mediating thrombosis and arterial injury1 Fulltext Access 4 Pages 2008
BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Fulltext Access 4 Pages 2008
Relationship between serum parathyroid hormone, vitamin D sufficiency, age, and calcium intake Fulltext Access 4 Pages 2008
Validity of serial milling-based imaging system for microdamage quantification Fulltext Access 4 Pages 2008
Lifetime absolute risk of hip and other osteoporotic fracture in Belgian women Fulltext Access 4 Pages 2008
Increased cortical remodeling after osteotomy causes posttraumatic osteopenia Fulltext Access 5 Pages 2008
Vertebral fracture assessment in healthy men: Prevalence and risk factors Fulltext Access 5 Pages 2008
Incidence and risk factors for low trauma fractures in men with prostate cancer Fulltext Access 5 Pages 2008
A novel mutation in LMX1B gene causes nail-patella syndrome in a large Chinese family Fulltext Access 5 Pages 2008
Osseous Hodgkin's lymphoma-review of literature and report of an unusual case presenting as a large ulcerofungating sternal mass Fulltext Access 5 Pages 2008
Peptide YY (PYY) levels and bone mineral density (BMD) in women with anorexia nervosa Fulltext Access 5 Pages 2008
Observer performance in diagnosing osteoporosis by dental panoramic radiographs: Results from the osteoporosis screening project in dentistry (OSPD) Fulltext Access 5 Pages 2008
Methylation status of fragile histidine triad (FHIT) gene and its clinical impact on prognosis of patients with myelodysplastic syndrome Fulltext Access 5 Pages 2008
Common features of myeloproliferative disorders with t(8;9)(p12;q33) and CEP110–FGFR1 fusion: Report of a new case and review of the literature Fulltext Access 5 Pages 2008
Increased expression of angiopoietin-2 characterizes early B-cell chronic lymphocytic leukemia with poor prognosis Fulltext Access 5 Pages 2008
Efficacy of decitabine in the treatment of patients with chronic myelomonocytic leukemia (CMML) Fulltext Access 5 Pages 2008
High incidence of tuberculosis after alemtuzumab treatment in Hong Kong Chinese patients Fulltext Access 5 Pages 2008
Acquired amegakaryocytic thrombocytopenia and pure red cell aplasia associated with an occult large granular lymphocyte leukemia Fulltext Access 5 Pages 2008
Immunoreactivity for cyclin D1 is a reliable marker of gene aberration in plasma cell myeloma but does not specify patients prognosis Fulltext Access 5 Pages 2008
Tetrasomy 21 as a sole acquired abnormality without GATA1 gene mutation in pediatric acute megakaryoblastic leukemia: A case report and review of the literature Fulltext Access 5 Pages 2008
Malignant hematopoietic cell lines: In vitro models for the study of Waldenström's macroglobulinemia Fulltext Access 5 Pages 2008
BCR-ABL, ETV6-RUNX1 and E2A-PBX1: Prevalence of the most common acute lymphoblastic leukemia fusion genes in Mexican patients Fulltext Access 5 Pages 2008
Blood counts at time of complete remission provide additional independent prognostic information in acute myeloid leukemia Fulltext Access 5 Pages 2008
Low erythropoietin production as non-oncogenic co-factor contributing to disease-manifestation in low-risk MDS: A hypothesis supported by unique case reports Fulltext Access 5 Pages 2008
Atypical chronic myeloid leukemia as defined in the WHO classification is a JAK2 V617F negative neoplasm Fulltext Access 5 Pages 2008
Clinicopathologic features and treatment outcome of primary breast diffuse large B-cell lymphoma Fulltext Access 5 Pages 2008
The significance of soluble HLA-G plasma levels as well as messenger HLA-G for B-cell chronic lymphocytic leukemia (B-CLL) Fulltext Access 5 Pages 2008
Treatment of myelodysplastic syndromes with 5q deletion before the lenalidomide era; the GFM experience with EPO and thalidomide Fulltext Access 5 Pages 2008
Segmental duplications involving the α-globin gene cluster are causing β-thalassemia intermedia phenotypes in β-thalassemia heterozygous patients Fulltext Access 5 Pages 2008
Adoptive cellular therapy for cytomegalovirus infection following allogeneic stem cell transplantation using virus-specific T cells Fulltext Access 5 Pages 2008
Nonmyeloablative allogeneic hematopoietic stem cell transplant using mismatched/haploidentical donors: A review Fulltext Access 5 Pages 2008
Overweight, insulin resistance and type II diabetes in type I Gaucher disease patients in relation to enzyme replacement therapy Fulltext Access 5 Pages 2008
CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin's lymphoma Fulltext Access 5 Pages 2008
A novel (Leu183Pro-)mutation in the HFE-gene co-inherited with the Cys282Tyr mutation in two unrelated Dutch hemochromatosis patients Fulltext Access 5 Pages 2008
A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia Fulltext Access 5 Pages 2008
Generation of T cell regulatory activity by plasmacytoid dendritic cells and tryptophan catabolism Fulltext Access 5 Pages 2008
Platelet signalling abnormalities in patients with type 2 diabetes mellitus: A review Fulltext Access 5 Pages 2008
BCL6 represses CHEK1 and suppresses DNA damage pathways in normal and malignant B-cells Fulltext Access 5 Pages 2008
Sumoylation and the function of CCAAT enhancer binding protein alpha (C/EBPα) Fulltext Access 5 Pages 2008
Development and evaluation of a reverse dot blot assay for the simultaneous detection of six common Chinese G6PD mutations and one polymorphism Fulltext Access 5 Pages 2008
Presence of cytosolic peroxiredoxin 2 in the erythrocyte membrane of patients with hereditary spherocytosis Fulltext Access 5 Pages 2008
A MLL-KIAA0284 fusion gene in a patient with secondary acute myeloid leukemia and t(11;14)(q23;q32) Fulltext Access 5 Pages 2008
Serum prohepcidin is associated with soluble transferrin receptor-1 but not ferritin in healthy post-menopausal women Fulltext Access 5 Pages 2008