# عنوان نوع فایل سایز فایل بازدید دانلود امتیاز قیمت (تومان)
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Expression of myelopoiesis-associated microRNA in bone marrow cells of atypical chronic myeloid leukaemia and chronic myelomonocytic leukaemia
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The role of routine imaging procedures in the detection of relapse of patients with Hodgkin lymphoma and aggressive non-Hodgkin lymphoma
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CLIPI: a new prognostic index for indolent cutaneous B cell lymphoma proposed by the International Extranodal Lymphoma Study Group (IELSG 11)
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Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1G208R mutation
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Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal)
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High prevalence of hepatitis B and hepatitis C virus infections in Korean patients with hematopoietic malignancies
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Overexpression of the EZH2, RING1 and BMI1 genes is common in myelodysplastic syndromes: relation to adverse epigenetic alteration and poor prognostic scoring
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Long-term follow-up of patients with chronic myeloid leukemia having received autologous stem cell transplantation
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CYP2B6 gene single nucleotide polymorphisms and leukemia susceptibility
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Sickle-cell disease and malaria: evaluation of seasonal intermittent preventive treatment with Sulfadoxine-pyrimethamine in Senegalese patients—a randomized placebo-controlled trial
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Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation
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Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study
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Contribution of VKORC1 and CYP2C9 polymorphisms in the interethnic variability of warfarin dose in Malaysian populations
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Impact of cytokine gene polymorphisms on risk and treatment outcomes of aplastic anemia
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The role of zinc protoporphyrin measurement in the differentiation between primary myelofibrosis and essential thrombocythaemia
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Leukemias induced by altered TRK-signaling are sensitive to mTOR inhibitors in preclinical models
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Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family
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Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease
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A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5پŒ-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis fa
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Oxidative stress contributes to hemolysis in patients with hereditary spherocytosis and can be ameliorated by fermented papaya preparation
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Hydralazine and magnesium valproate as epigenetic treatment for myelodysplastic syndrome. Preliminary results of a phase-II trial
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Myeloid growth factors in acute myeloid leukemia: systematic review of randomized controlled trials
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Dysmetabolic hyperferritinemia is associated with normal transferrin saturation, mild hepatic iron overload, and elevated hepcidin
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Deferasirox effectively decreases iron burden in patients with double heterozygous HbS/â-thalassemia
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Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system
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Expression of myelopoiesis-associated microRNA in bone marrow cells of atypical chronic myeloid leukaemia and chronic myelomonocytic leukaemia

Expression of myelopoiesis-asso ...

The microRNA/miR deregulation in BCR-ABLnegative myelodysplastic-myeloproliferative neoplasms (MDS/MPN) is not known. Myelopoiesis-associated miR-1 ...

189.35 KB
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The role of routine imaging procedures in the detection of relapse of patients with Hodgkin lymphoma  and aggressive non-Hodgkin lymphoma

The role of routine imaging pro ...

Despite improved initial therapies, a subgroup of patients with aggressive non-Hodgkin (A-NHL) and Hodgkin lymphomas (HL) will relapse after first r ...

170.78 KB
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CLIPI: a new prognostic index for indolent cutaneous B cell lymphoma proposed by the International Extranodal Lymphoma Study Group (IELSG 11)

CLIPI: a new prognostic index f ...

Indolent primary cutaneous B cell lymphomas (PCBCL) generally have a good prognosis, but they often relapse leading in some cases to extracutaneous ...

245.04 KB
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Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1G208R mutation

Long-term outcome of hemizygous ...

The transcriptional regulator GATA1 is crucially involved in megakaryocytopoiesis and erythropoiesis. Mutations of the gene which is located on the ...

دانلود 1
643.92 KB
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Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal)

Prevalence of H63D, S65C, and C ...

Hereditary HFE Hemochromatosis is an inherited disorder of iron metabolism that results from mutations in the HFE gene. Almost all patients with her ...

99.69 KB
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High prevalence of hepatitis B and hepatitis C virus infections in Korean patients with hematopoietic malignancies

High prevalence of hepatitis B ...

We performed a large case–control study (3,932 cases, 15,562 controls) to investigate the association of hepatitis B virus (HBV) and hepatitis C vir ...

109.81 KB
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Overexpression of the EZH2, RING1 and BMI1 genes is common in myelodysplastic syndromes: relation to adverse epigenetic alteration and poor prognostic scoring

Overexpression of the EZH2, RIN ...

Epigenetics refers to the study of clonally inherited changes in gene expression without accompanying genetic changes. Previous research on the epig ...

348.51 KB
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Long-term follow-up of patients with chronic myeloid leukemia having received autologous stem cell  transplantation

Long-term follow-up of patients ...

Prior to introduction of imatinib mesylate, the median survival of chronic myeloid leukemia (CML) patients was approximately 60 months and the stand ...

208.90 KB
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CYP2B6 gene single nucleotide polymorphisms and leukemia susceptibility

CYP2B6 gene single nucleotide p ...

CYP2B6 is a highly variable and polymorphic cytochrome P450 enzyme which plays a vital role in the degradation of some endogenous metabolites, xenob ...

203.14 KB
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Sickle-cell disease and malaria: evaluation of seasonal intermittent preventive treatment with  Sulfadoxine-pyrimethamine in Senegalese patients—a randomized placebo-controlled trial

Sickle-cell disease and malaria ...

Sickle-cell disease (SCD) patients are at high risk of developing malaria which is a major contributor to morbidity andmortality in this disease. In ...

111.05 KB
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Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation

Severe congenital neutropenia i ...

We have analysed a family with nine congenital neutropenia patients in four generations, several of which we have studied in a long-term follow-up o ...

217.88 KB
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Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis:  results of a multicentre study

Additional erythrocytic and ret ...

Hereditary spherocytosis (HS) is characterised by weakened vertical linkages between the membrane skeleton and the red blood cell’s lipid bilayer, l ...

341.00 KB
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Contribution of VKORC1 and CYP2C9 polymorphisms in the interethnic variability of warfarin dose in Malaysian populations

Contribution of VKORC1 and CYP2 ...

Within the Asian populations, Indian patients had been reported to require higher warfarin dose compared with the Chinese and Malay patients, and th ...

139.50 KB
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Impact of cytokine gene polymorphisms on risk and treatment outcomes of aplastic anemia

Impact of cytokine gene polymor ...

Autoreactive cytotoxic T cells play a key role in the pathogenesis of aplastic anemia (AA) by myelosuppressive cytokines including interferon-gamma, ...

239.30 KB
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The role of zinc protoporphyrin measurement in the differentiation between primary myelofibrosis  and essential thrombocythaemia

The role of zinc protoporphyrin ...

The differentiation between primary myelofibrosis (PMF) and essential thrombocythaemia (ET) may be difficult especially in early-stage disease. In P ...

185.47 KB
رایگان
Leukemias induced by altered TRK-signaling are sensitive to mTOR inhibitors in preclinical models

Leukemias induced by altered TR ...

Rapamycin is a potent allosteric mTORC1 inhibitor with clinical applications as an anticancer agent. However, only a fraction of cancer patients res ...

597.84 KB
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Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family

Molecular characterization of a ...

Over 80% of the α-thalassemia cases in southern China are caused by large deletions involving the α-globin gene cluster on chromosome 16p13.3. Here, ...

311.81 KB
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Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease

Cost-effectiveness of adenotons ...

In children with sickle cell disease (SCD), adenotonsillar hypertrophy or recurrent tonsillitis are frequently linked with an increased risk of obst ...

128.78 KB
رایگان
A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5پŒ-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis fa

A prospective study to assess t ...

This prospective study was carried out to assess the usefulness of five laboratory tests in the diagnosis of hereditary spherocytosis (HS), based on ...

دانلود 1
450.90 KB
رایگان
Oxidative stress contributes to hemolysis in patients with hereditary spherocytosis and can be ameliorated by fermented papaya preparation

Oxidative stress contributes to ...

In the present study, we questioned the role of oxidative stress in hereditary spherocytosis (HS), where red blood cells (RBC) have a shortened surv ...

230.13 KB
رایگان
Hydralazine and magnesium valproate as epigenetic treatment for myelodysplastic syndrome.  Preliminary results of a phase-II trial

Hydralazine and magnesium valpr ...

Decitabine and azacitidine, two DNA methyltransferase (DNMT) inhibitors, are the current standard of treatment for myelodysplastic syndrome (MDS). H ...

220.92 KB
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Myeloid growth factors in acute myeloid leukemia: systematic review of randomized controlled trials

Myeloid growth factors in acute ...

Randomized controlled trials (RCT) investigating administration of colony-stimulating factors (CSF) during or after chemotherapy in acute myeloid le ...

404.43 KB
رایگان
Dysmetabolic hyperferritinemia is associated with normal transferrin saturation, mild hepatic iron overload, and elevated hepcidin

Dysmetabolic hyperferritinemia ...

Hyperferritinemia is common in individuals with the metabolic syndrome (dysmetabolic hyperferritinemia), but its pathophysiology and the degree to w ...

99.71 KB
رایگان
Deferasirox effectively decreases iron burden in patients with double heterozygous HbS/â-thalassemia

Deferasirox effectively decreas ...

Iron overload is present in several cases of double heterozygous sickle-cell/beta-thalassemia (HbS/β-thal). Deferasirox is an orally administered ir ...

136.38 KB
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Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system

Quantitative analysis of Hb Bar ...

It has long been recognized that the presence of hemoglobin (Hb) Bart’s in newborn’s blood is associated with α-thalassemia. However, the automated ...

311.20 KB
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