• 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
• ATP-Binding Cassette Transporter of Clinical Significance: Sideroblastic 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
• Diagnostic challenges and proposed classification of myeloid neoplasms with overlapping features of thrombocytosis, ring sideroblasts and concurrent del(5q) and <em>SF3B1</em> mutations
• Dolutegravir-induced acquired sideroblastic anemia in a HIV positive patient: A challenging hematologic complication
• Dolutegravir-induced severe sideroblastic anemia
• Elucidating the Role of Human ALAS2 C-terminal Mutations Resulting in Loss of Function and Disease
• Erythropoiesis-hepcidin-iron axis in patients with X-linked sideroblastic anaemia: An explorative biomarker study
• Hematologic Manifestations in Primary Mitochondrial Diseases
• Hemochromatosis
• Leber's hereditary optic neuropathy like disease in <em>MT-ATP6</em> variant m.8969G&gt;A
• Luspatercept as Potential Treatment for Congenital Sideroblastic Anemia
• Luspatercept enhances hemoglobin levels in a Chinese boy with congenital sideroblastic anemia: A case report
• 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
• Murine models of erythroid 5ALA synthesis disorders and their conditional synthetic lethal dependency on pyridoxine
• 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
• Severe pulmonary arterial hypertension in congenital sideroblastic anemia from PUS1 mutation - a case report
• 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
• 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
• Transfusion Iron Overload
• 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
• Using portable X-ray fluorescence elemental analysis to explore porous skeletal lesions: Interplay of sex, age at death, and cause of death
• Zinc-Containing Over-The-Counter Product Causing Sideroblastic Anemia and Neutropenia