Disease: Pure red cell aplasia
- 15q26 deletion syndrome with pure red cell aplastic anemia: a case report
- A Case of Suspected Pure Red Cell Aplasia Due to Nivolumab Treatment for Unresectable Esophageal Cancer
- A case report on deficiency of adenosine deaminase 2 with relapse-remission course and analysis of genotype-phenotype correlation
- A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in Iran
- A De Novo Frameshift Mutation in RPL5 with Classical Phenotype Abnormalities and Worsening Anemia Diagnosed in a Young Adult-A Case Report and Review of the Literature
- A late relapse thymoma and pure red cell aplasia case with an over 5 years of clinical response under everolimus
- A nomogram model for predicting the efficacy of cyclosporine in patients with pure red cell aplasia
- Bidirectional ABO Mismatch Is Associated With Elevated Mortality in Hematopoietic Stem Cell Transplantation: Insights From a Single-Center Experience
- Case report: Successful treatment with daratumumab for pure red cell aplasia in a patient with mixed lymphoid chimerism after ABO-mismatched stem cell transplant for sickle cell disease
- Clinical and immune features of human parvovirus B19 infection in allogeneic stem cell transplantation recipients: A retrospective monocentric study
- Clinical characteristics and prognosis of 21 patients with thymoma-associated pure red cell aplasia
- Comparison of Cyclosporine A and Cyclosporine A Combined with Corticosteroid in the Treatment of Acquired Pure Red Cell Aplasia
- Deficiency of Adenosine Deaminase 2: Clinical Manifestations, Diagnosis, and Treatment
- Diamond-Blackfan anemia with very late and fatal onset aplasia in a 55-year-old patient with RPL11 mutation
- Diamond-Blackfan anemia, the archetype of ribosomopathy: How distinct is it from the other constitutional ribosomopathies?
- Efficacy and safety of Daratumumab for the treatment of ABO-incompatible pure red cell aplasia after allogenic HSCT: report from SFGM-TC
- Efficacy and safety of daratumumab in pure red cell aplasia after allogeneic transplantation: Dutch real-world data
- En mann i 40-årene med transfusjonskrevende anemi
- Et barn med langvarig anemi
- Functional autoantibodies: Definition, mechanisms, origin and contributions to autoimmune and non-autoimmune disorders
- Gilteritinib combined with venetoclax and azacitidine for relapsed acute myeloid leukemia cocurrent with pure red cell aplasia after allogeneic hematopoietic stem cell transplantation: a case report
- Haploinsufficiency of the essential gene <em>Rps12</em> causes defects in erythropoiesis and hematopoietic stem cell maintenance
- Hematologic Manifestations of Parvovirus B19 Infection
- High expression of NADH Ubiquinone Oxidoreductase Subunit B11 induces catheter-associated venous thrombosis on continuous blood purification
- HLA-B*46:01:01:01 and HLA-DRB1*09:01:02:01 are associated with anti-rHuEPO-induced pure red cell aplasia
- Identification of novel mutations in patients with Diamond-Blackfan anemia and literature review of RPS10 and RPS26 mutations
- Immune Checkpoint Inhibitor-Induced Pure Red Cell Aplasia: A Review of 2 Cases in Metastatic Melanoma
- Immune-mediated hemolytic anemia and pure red cell aplasia in a Jack Russell Terrier during treatment for hypoadrenocorticism
- Insights from a Case of Good's Syndrome (Immunodeficiency with Thymoma)
- Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report
- Large granular lymphocytic leukemia and its association with immune dysregulation
- Monoclonal Gammopathy of Anemic Significance? Resolution of Pure Red Cell Aplasia With Daratumumab-Based Therapy
- Monolobated megakaryocytes in Diamond-Blackfan anemia with RPL5 mutation at disease presentation mimicking myelodysplastic syndrome
- Niraparib-induced pure red cell aplasia
- Non-immune hydrops fetalis caused by Diamond-Blackfan anaemia and a mutation of the RPL15 gene
- Normal Erythroid Precursors in Diamond-Blackfan Anemia: A Rare Case Highlighting Challenges That Remain
- p53 in the Molecular Circuitry of Bone Marrow Failure Syndromes
- Patients with acquired pure red cell aplasia respond to PI3Kdelta inhibitor rapidly
- Perspectives of current understanding and therapeutics of Diamond-Blackfan anemia
- Positive response of a hemodialysis patient with pure red cell aplasia on recombinant human erythropoietin therapy to cyclosporine and Roxadustat
- Pure red cell aplasia and minimal residual disease conversion associated with immune reconstitution in a patient with high-risk multiple myeloma
- Pure Red Cell Aplasia Associated With Thymoma
- Pure Red Cell Aplasia Encountered in a Tertiary Care Hematology Laboratory: A Series of Nine Distinctive Cases
- Pure Red Cell Aplasia Induced by Atezolizumab in a Patient with Small-Cell Lung Cancer Successfully Treated with Steroid Therapy: A Case Report
- Pure red cell aplasia occurring during ibrutinib therapy for chronic lymphocytic leukemia
- Pure Red Cell Aplasia Secondary to Parvovirus B19 Infection as a Rare Cause of Anemia in a Dialysis Patient: A Case Report
- Pure red cell aplasia: The second hundred years
- Real-life use of mTOR inhibitor-based therapy in adults with autoimmune cytopenia highlights strong efficacy in relapsing/refractory multi-lineage autoimmune cytopenia
- Refractory Pure Red Blood Cell Aplasia Secondary to Major ABO-Incompatible Allogeneic Stem Cell Transplantation Successfully Treated With Daratumumab
- Resistant anemia in a kidney transplant recipient: Pure red cell aplasia due to parvovirus B19 infection
- Role of Anti-CD38 Monoclonal Antibodies in the Treatment of Adult Immune Hematological Diseases
- Secondary Pure Red Cell Aplasia During Daratumumab/ Hyaluronidase Therapy for Multiple Myeloma
- Single-cell RNA sequencing reveals abnormal transcriptome signature of erythroid progenitors in pure red cell aplasia
- Successful Clozapine Rechallenge After Clozapine-Induced Severe Anemia: A Case Report
- Successful treatment of a pure red cell aplasia patient following ABO-mismatched hematopoietic stem cell transplantation from a sibling donor with multiple sclerosis
- Successful treatment pure red cell aplasia after ABO major mismatched allogeneic hematopoietic stem cell transplantation with avatrombopag and low dose rituximab
- T-cell large granular lymphocytic leukemia in Vietnam: Using microscope-to-screen videoconferencing to improve diagnosis
- T-cell large granular lymphocytic leukemia with low-grade bone marrow involvement complicated by acquired pure red cell aplasia
- Targeting of Calbindin 1 rescues erythropoiesis in a human model of Diamond Blackfan anemia
- The transcriptomic landscape of normal and ineffective erythropoiesis at single-cell resolution
- Transient erythroblastopenia due to a GATA1 variant in an infant female
- Treatment strategy for acquired pure red cell aplasia: a systematic review and meta-analysis
- Unearthing FLVCR1a: tracing the path to a vital cellular transporter
- Unusual Presentation of B-Cell Chronic Lymphocytic Leukemia Accompanied by Pure Red Cell Aplasia: Case Report
- Waldenström macroglobulinemia with secondary pure red cell aplasia in a patient with metastatic castrate resistant prostate cancer receiving an immune checkpoint inhibitor: a case report