Anemia: Vol 2012, No 1

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Traditional Herbal Management of Sickle Cell Anemia: Lessons from Nigeria

Relationship between Plasma Ferritin Level and Siderocyte Number in Splenectomized β-Thalassemia/HbE Patients

Management of Anemia of Inflammation in the Elderly

A Molecular, Genetic, and Diagnostic Spotlight on Fanconi Anemia

β-Thalassemia: New Therapeutic Modalities, Genetics, Complications, and Quality of Life

Safety and Efficacy of Intravenous Ferric Carboxymaltose (750 mg) in the Treatment of Iron Deficiency Anemia: Two Randomized, Controlled Trials

Reduced PKC α Activity Induces Senescent Phenotype in Erythrocytes

Sickle Cell Disease: Genetics, Cellular and Molecular Mechanisms, and Therapies

An Epidemiological Study of Anemia and Renal Dysfunction in Patients Admitted to ICUs across the United States

Health-Related Quality of Life, Treatment Satisfaction, Adherence and Persistence in β-Thalassemia and Myelodysplastic Syndrome Patients with Iron Overload Receiving Deferasirox: Results from the EPIC Clinical Trial

Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell Anaemia

Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing

Induction of Fetal Hemoglobin In Vivo Mediated by a Synthetic γ-Globin Zinc Finger Activator

Sickling Cells, Cyclic Nucleotides, and Protein Kinases: The Pathophysiology of Urogenital Disorders in Sickle Cell Anemia

Fanconi Anemia Proteins and Their Interacting Partners: A Molecular Puzzle

Spatiotemporal Dysfunction of the Vascular Permeability Barrier in Transgenic Mice with Sickle Cell Disease

Hematopoietic Stem Cell Function in a Murine Model of Sickle Cell Disease

Integrating Interactive Web-Based Technology to Assess Adherence and Clinical Outcomes in Pediatric Sickle Cell Disease

A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites

Diagnosis of Fanconi Anemia: Mutation Analysis by Next-Generation Sequencing

Loss of Ercc1 Results in a Time- and Dose-Dependent Reduction of Proliferating Early Hematopoietic Progenitors

A DOG’s View of Fanconi Anemia: Insights from C. elegans

Physiopathology of Bone Modifications in β-Thalassemia

Evaluation of Hematological Parameters in Partial Exchange and Packed Cell Transfusion in Treatment of Severe Anemia in Pregnancy

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

Targeting the Fanconi Anemia Pathway to Identify Tailored Anticancer Therapeutics

Elevated Circulating Angiogenic Progenitors and White Blood Cells Are Associated with Hypoxia-Inducible Angiogenic Growth Factors in Children with Sickle Cell Disease

Chromosomal Aberrations Associated with Clonal Evolution and Leukemic Transformation in Fanconi Anemia: Clinical and Biological Implications

Disrupted Signaling through the Fanconi Anemia Pathway Leads to Dysfunctional Hematopoietic Stem Cell Biology: Underlying Mechanisms and Potential Therapeutic Strategies

Towards a Molecular Understanding of the Fanconi Anemia Core Complex

FK228 Analogues Induce Fetal Hemoglobin in Human Erythroid Progenitors

Hemin Augments Growth and Hemoglobinization of Erythroid Precursors from Patients with Diamond-Blackfan Anemia

Correlation of Oxidative Stress with Serum Trace Element Levels and Antioxidant Enzyme Status in Beta Thalassemia Major Patients: A Review of the Literature

Prevalence of Anaemia and Evaluation of Transferrin Receptor (sTfR) in the Diagnosis of Iron Deficiency in the Hospitalized Elderly Patients: Anaemia Clinical Studies in Chile

Utilization Patterns of IV Iron and Erythropoiesis Stimulating Agents in Anemic Chronic Kidney Disease Patients: A Multihospital Study

Association of Oxidative Stress Markers with Atherogenic Index of Plasma in Adult Sickle Cell Nephropathy

Sickle Cell Disease Activates Peripheral Blood Mononuclear Cells to Induce Cathepsins K and V Activity in Endothelial Cells

Cobalamin and Folic Acid Status in Relation to the Etiopathogenesis of Pancytopenia in Adults at a Tertiary Care Centre in North India

Eryptotic Phenotype in Chronic Myeloid Leukemia: Contribution of Neutrophilic Cathepsin G

Thalassemic DNA-Containing Red Blood Cells Are under Oxidative Stress

Prevalence of Anemia and Risk of Adverse Bleeding Effect of Drugs: Implication for Therapy

Risk Factors for Anemia among Brazilian Infants from the 2006 National Demographic Health Survey

Intracranial Blood Flow Velocity in Patients with β-Thalassemia Intermedia Using Transcranial Doppler Sonography: A Case-Control Study

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