Sideroblastic Anemia Latest Advances

Find the Latest Research About Sideroblastic Anemia

Last Updated: 09/26/2026

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Found 2255 publications

VEXAS Syndrome：Report of One Case.

VEXAS Syndrome：Report of One Case.

Journal: Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae
Published: August 27, 2026

Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Journal: Diagnostics (Basel, Switzerland)
Published: July 12, 2026

Vitamin B6 deficiency as a cause of erythropoietin-stimulating agent-resistant anemia in hemodialysis patients: A report of two cases.

Vitamin B6 deficiency as a cause of erythropoietin-stimulating agent-resistant anemia in hemodialysis patients: A report of two cases.

Journal: Internal medicine (Tokyo, Japan)
Published: July 12, 2026

Clinical Characteristics and Prognosis Analysis of MDS-RS Patients with Wild-Type SF3B1

Clinical Characteristics and Prognosis Analysis of MDS-RS Patients with Wild-Type SF3B1

Journal: Zhongguo shi yan xue ye xue za zhi
Published: June 02, 2026

Facial Dysmorphism and Severe Vascular Phenotype in TRNT1 Deficiency with Concomitant Antithrombin III Deficiency.

Facial Dysmorphism and Severe Vascular Phenotype in TRNT1 Deficiency with Concomitant Antithrombin III Deficiency.

Journal: Journal of clinical immunology
Published: May 10, 2026

Expanding the spectrum of Sideroblastic Anemia with B-cell Immunodeficiency, Periodic Fever and Developmental Delay (SIFD) syndrome: a case report with new clinical insights and novel genetic variant.

Expanding the spectrum of Sideroblastic Anemia with B-cell Immunodeficiency, Periodic Fever and Developmental Delay (SIFD) syndrome: a case report with new clinical insights and novel genetic variant.

Journal: Frontiers in immunology
Published: May 08, 2026

SLC25A38 gene modification mediated by CRISPR/Cas9 in HEK293T cell line.

SLC25A38 gene modification mediated by CRISPR/Cas9 in HEK293T cell line.

Journal: Journal of applied genetics
Published: May 06, 2026

Multi-generational mitochondrial complex V deficiency due to the recurrent ATP5F1A c.620G>A (p.Arg207His) pathogenic variant: A novel family and a review of the literature.

Multi-generational mitochondrial complex V deficiency due to the recurrent ATP5F1A c.620G>A (p.Arg207His) pathogenic variant: A novel family and a review of the literature.

Journal: Molecular genetics and metabolism
Published: April 20, 2026

A diagnostic pitfall in iron-refractory microcytic hypochromic anemia with acquired ring sideroblasts initially treated as iron deficiency anemia-a case report.

A diagnostic pitfall in iron-refractory microcytic hypochromic anemia with acquired ring sideroblasts initially treated as iron deficiency anemia-a case report.

Journal: Frontiers in medicine
Published: March 25, 2026

Successful Outcome of Haploidentical Hematopoietic Stem Cell Transplantation in X-Linked Sideroblastic Anemia.

Successful Outcome of Haploidentical Hematopoietic Stem Cell Transplantation in X-Linked Sideroblastic Anemia.

Journal: Pediatric blood & cancer
Published: March 09, 2026

Congenital sideroblastic anemia: Unravelling molecular pathogenesis and advancing precision therapeutics.

Congenital sideroblastic anemia: Unravelling molecular pathogenesis and advancing precision therapeutics.

Journal: Gene
Published: February 02, 2026

Post-transplant ring sideroblasts are common in haploidentical peripheral blood stem cell transplantation but not linked to SF3B1 mutations.

Post-transplant ring sideroblasts are common in haploidentical peripheral blood stem cell transplantation but not linked to SF3B1 mutations.

Journal: Clinical chemistry and laboratory medicine
Published: January 16, 2026
Showing 1-12 of 2,255

Last Updated: 09/26/2026