Disease: Anemia- Sideroblastic
- A Novel <em>ALAS2</em> Mutation Causes Congenital Sideroblastic Anemia
- A Novel ALAS2 Mutation Causes Congenital Sideroblastic Anemia
- A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country
- Anemia: Microcytic Anemia
- Case report: Muscle involvement in a Chinese patient with <em>TRNT1</em>-related disorder
- Case report: Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay: Three cases and a literature review
- Clinical characteristics of Japanese patients with myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis
- Comprehensive genomic analysis identifies a diverse landscape of sideroblastic and non-sideroblastic iron related anemias with novel and pathogenic variants in an iron deficient endemic setting
- Comprehensive Genomic Analysis Identifies a Diverse Landscape of Sideroblastic and Nonsideroblastic Iron-Related Anemias with Novel and Pathogenic Variants in an Iron-Deficient Endemic Setting
- Congenital sideroblastic anemia with vacuolated bone marrow precursors secondary to SLC25A38 mutation-A great mimicker of Pearson syndrome
- Copper Deficiency as Wilson's Disease Overtreatment: A Systematic Review
- Deconvoluting the Complexity of Congenital Sideroblastic Anemias through Genetic and Functional Profiling
- Dolutegravir-induced acquired sideroblastic anemia in a HIV positive patient: A challenging hematologic complication
- Dolutegravir-induced severe sideroblastic anemia
- Erythropoiesis-hepcidin-iron axis in patients with X-linked sideroblastic anaemia: An explorative biomarker study
- Hemochromatosis
- Luspatercept as Potential Treatment for Congenital Sideroblastic Anemia
- Luspatercept for the treatment of congenital sideroblastic anemia: Two case reports
- Mitochondrial DNA Deletion Syndromes
- Mitochondrial tRNA pseudouridylation governs erythropoiesis
- MLASA-1: A Rare Cause of Myopathy with Sideroblastic Anemia
- Myelodysplastic Neoplasms (MDS) with Ring Sideroblasts or <em>SF3B1</em> Mutations: The Improved Clinical Utility of World Health Organization and International Consensus Classification 2022 Definitions, a Single-Centre Retrospective Chart Rev
- Pristinamycin-induced sideroblastic anaemia
- Pseudouridine synthase 1 regulates erythropoiesis via transfer RNAs pseudouridylation and cytoplasmic translation
- Real-world efficacy and safety of luspatercept and predictive factors of response in patients with lower risk myelodysplastic syndromes with ring sideroblasts
- Refractory Anemia With Ring Sideroblasts
- Refractory Anemia With Ring Sideroblasts
- Role of aberrant RNA splicing in acquired sideroblastic anemia
- Sideroblastic Anemia
- Sideroblastic Anemia
- Single Large-Scale Mitochondrial DNA Deletion Syndromes
- Spontaneous, simultaneous bilateral osteonecrosis of the femoral heads in a patient with sideroblastic anaemia with B-cell immunodeficiency, periodic fever and developmental delay syndrome
- Teaching NeuroImage: Glutaredoxin-5-Associated Variant Nonketotic Hyperglycinemia
- The E592K variant of SF3B1 creates unique RNA missplicing and associates with high-risk MDS without ring sideroblasts
- Three siblings with variable degrees of neuromuscular involvement and congenital sideroblastic anemia: A peculiar phenotype and a surprise genotypic explanation
- TRNT-1 Deficiency Is Associated with Loss of tRNA Integrity and Imbalance of Distinct Proteins
- Two new mutations in the GLRX5 gene cause sideroblastic anemia