• 5'UTR variants of ribosomal protein S19 transcript determine translational efficiency: implications for Diamond-Blackfan anemia and tissue variability
• A 2-Year-Old Child with Alazami Syndrome with Newly Reported Findings of Immune Deficiency, Periventricular Nodular Heterotopia, and Stroke; Broadening the Phenotype of Alazami
• A case of severe acute hepatitis a complicated with pure red cell aplasia
• A Case Report on Transient Erythroblastopenia of Childhood in a Female Pediatric Patient
• A child with persistent anaemia
• A Novel Deletion in the RPL5 Gene in a Lebanese Child With Diamond Blackfan Anemia Unresponsive to Steroid Treatment
• A novel nucleolar protein interacts with ribosomal protein S19
• A transgenic mouse model demonstrates a dominant negative effect of a point mutation in the RPS19 gene associated with Diamond-Blackfan anemia
• Acute erythroblastopenia due to Parvovirus B19 revealing hereditary spherocytosis
• Acute pericarditis and transient erythroblastopenia associated with human parvovirus B19 infection
• Acute polyarthritis during a parvovirus B19 primary infection
• Advances in human B19 erythrovirus biology
• Adverse drug reactions of strontium ranelate(Protelos(®) in France
• Amicrobial pustulosis of the skin folds and autoimmune erythroblastopenia
• An RNA interference model of RPS19 deficiency in Diamond-Blackfan anemia recapitulates defective hematopoiesis and rescue by dexamethasone: identification of dexamethasone-responsive genes by microarray
• An uncommon presentation of COVID-19: concomitant acute pulmonary embolism, spontaneous tension pneumothorax, pneumomediastinum and subcutaneous emphysema (a case report)
• Autoimmune hemolytic anemia and autoimmune neutropenia in a child with erythroblastopenia of childhood (TEC) caused by human herpesvirus-6 (HHV-6)
• BLNK mutation associated with T-cell LGL leukemia and autoimmune diseases: Case report in hematology
• Breath-holding spells occur disproportionately more often in children with transient erythroblastopenia
• Carbamazepine-induced hemolytic and aplastic crises associated with reduced glutathione peroxidase activity of erythrocytes
• Case Report: Successful Treatment of Steroid-Refractory Immune Checkpoint Inhibitor-Related Pure Red Cell Aplasia With Cyclosporin
• Classic transient erythroblastopenia of childhood with human parvovirus B19 genome detection in the blood and bone marrow
• Clinicopathological associations of acquired erythroblastopenia
• Concomitant transient erythroblastopenia of childhood with neonatal hepatitis
• Darbepoetin alfa: new indication/new dosage. No proven advantage in chemotherapy-induced anaemia
• Defective ribosomal protein gene expression alters transcription, translation, apoptosis, and oncogenic pathways in Diamond-Blackfan anemia
• Deficient RPS19 protein production induces cell cycle arrest in erythroid progenitor cells
• Deformation of erythroblasts in transient erythroblastopenia of childhood caused by HHV-6
• Dermatological Toxicities of Bruton's Tyrosine Kinase Inhibitors
• Diagnosing Transient Erythroblastopenia of Childhood: A Review for Pediatricians
• Diamond-Blackfan anemia
• Diamond-Blackfan anemia
• Diamond-Blackfan anemia associated with beta-thalassemia trait
• Diamond-Blackfan anemia reveals the dark side of ribosome biogenesis
• Diamond-Blackfan anemia, ribosome and erythropoiesis
• Discrepancies in ICD-9/ICD-10-based codes used to identify three common diseases in cancer patients in real-world settings and their implications for disease classification in breast cancer patients and patients without cancer: a literature review and des
• Dual functions of the C5a receptor as a connector for the K562 erythroblast-like cell-THP-1 macrophage-like cell island and as a sensor for the differentiation of the K562 erythroblast-like cell during haemin-induced erythropoiesis
• Ectopic atrial tachycardia in an infant with transient erythroblastopenia of childhood
• Epoetin in haemodialysis patients: impact of change from subcutaneous to intravenous routes of administration
• Erythroblastopenia and primary myelofibrosis: a very rare association (a case report)
• Erythroblastopenia in a critically ill influenza patient
• Et barn med langvarig anemi
• Etiologies and Outcomes of Normocytic Anemia in Children
• Functionally impaired RPL8 variants associated with Diamond-Blackfan anemia and a Diamond-Blackfan anemia-like phenotype
• Genetic variants in the noncoding region of RPS19 gene in Diamond-Blackfan anemia: potential implications for phenotypic heterogeneity
• Glucose-6-phosphate dehydrogenase deficiency: the added value of cytology
• Gradual processing of the ITS1 from the nucleolus to the cytoplasm during synthesis of the human 18S rRNA
• Graft failure, poor graft function erythroblastopenia: Actualization of definitions, diagnosis and treatment: Guidelines from the SFGM-TC
• How many times can parvovirus B19-related anemia recur in solid organ transplant recipients?
• Immune aregenerative anemia without erythroblastopenia: a previously undescribed condition
• Impaired ribosome biogenesis in Diamond-Blackfan anemia
• Isoniazid-induced Pure Red Cell Aplasia in a Patient with Sarcoidosis: A Patient Summary and Review of the Literature
• Late-onset refractory hemolytic anemia in siblings treated for methionine synthase reductase deficiency: A rare complication possibly prevented by hydroxocobalamin dose escalation?
• Leg ulcers in patients with sickle-cell disease in Libreville (Gabon): clinical aspects and management
• Management of graft failure and erythroblastopenia in patients undergoing allogeneic hematopoietic stem cell transplantation: Guidelines from the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC)
• Management of thymoma associated autoimmune pure red cell aplasia: Case report and systematic review of the literature
• Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience
• Myelodysplastic syndrome with erythroblastopenia
• Ockham's razor defeated: about two atypical cases of hemolytic uremic syndrome
• Parvovirus B19 infection after plasma exchange for myasthenia gravis
• Parvovirus B19 infection in Tunisian patients with sickle-cell anemia and acute erythroblastopenia
• Parvovirus B19 Infection Mimicking Juvenile Myelomonocytic Leukemia in an Immunocompetent Child
• Pregnancy induced erythroblastopenia: about a case and review of the literature
• Prenatal parvovirus B19 infection in fetus
• Primary cutaneous T cell lymphoma with bone marrow infiltration and erythroblastopenia--a rare association
• Proliferative glomerulonephritis and erythroblastopenia associated with Bartonella quintana endocarditis
• Pure red cell anaemia secondary to medullary B cell chronic lymphoproliferative disorders. A rare case
• Pure red cell aplasia and hypogammaglobulinemia after administration of Dioscorea rhizome and Poria cocos
• Pure red cell aplasia associated with autoimmune hepatitis successfully treated with cyclosporine A
• Pure Red Cell Aplasia Caused by Azathioprine
• Pure Red Cell Aplasia Encountered in a Tertiary Care Hematology Laboratory: A Series of Nine Distinctive Cases
• Pure red cell aplasia with isolated human herpes virus 6 infection of bone marrow in postcardiac transplant patient
• Redistribution of iron towards deposits in erythroblastopenic anemia as a consequence of decreased erythroferrone production
• Reduced gene expression of clustered ribosomal proteins in Diamond-Blackfan anemia patients without RPS19 gene mutations
• Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1
• Ribosomal protein mutations in Diamond-Blackfan anemia: might they operate upstream from protein synthesis?
• Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia
• Rpl5-Inducible Mouse Model for Studying Diamond-Blackfan Anemia
• SLC29A3 mutation in a patient with syndromic diabetes with features of pigmented hypertrichotic dermatosis with insulin-dependent diabetes, H syndrome and Faisalabad histiocytosis
• Spectrum of pure red cell aplasia in adult population of north-west India
• Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia
• Supporting diagnostic decisions using hybrid and complementary data mining applications: a pilot study in the pediatric emergency department
• Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation
• Targeted resequencing and analysis of the Diamond-Blackfan anemia disease locus RPS19
• The problem of acquired aplastic anaemia
• The pure red cell aplasia in children (observation 2010-2012 years)
• Thymoma and autoimmune diseases
• Transfusion-dependent anaemia of undetermined origin: a distinctive syndrome in paediatric medical tourism
• Transient aplastic crisis triggered by parvovirus B19 in a family with hereditary spherocytosis
• Transient erythroblastopenia due to a GATA1 variant in an infant female
• Transient erythroblastopenia of childhood after COVID-19 infection: a case report
• Transient erythroblastopenia of childhood in siblings: case report and review of the literature
• Transient erythroblastopenia of childhood is an underdiagnosed and self-limiting disease
• Transient Erythroblastopenia of Childhood With Exanthema Subitum Caused by Human Herpesvirus 7
• Transient Erythroblastopenia of Childhood: A Review for the Pediatric Emergency Medicine Physician
• Transient Erythroblastopenia: An Unusual Manifestation of Macrophage Activation Syndrome in Kawasaki Disease
• Update of the human parvovirus B19 biology
• Utility of Whole Exome Sequencing in the Early Diagnosis of Atypical Diamond-Blackfan Anemia
• What is antibody-mediated pure red cell aplasia (PRCA)?
• What is new in iron overload?