Anemia

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 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

Anemia

Table of Contents

Table of Contents: 2012

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 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

Anemia

Table of Contents

Table of Contents: 2012

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

Reduced PKC Activity Induces Senescent Phenotype in Erythrocytes