Sideroblastic Anemia Latest Advances

Find the Latest Research About Sideroblastic Anemia

Last Updated: 11/08/2026

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Found 2260 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

A New Gain-of-Function NLRP1 Variant Is Associated with Inflammasome Activation and Disease Severity in SLC25A38 Congenital Sideroblastic Anemia Case Report.

A New Gain-of-Function NLRP1 Variant Is Associated with Inflammasome Activation and Disease Severity in SLC25A38 Congenital Sideroblastic Anemia Case Report.

Journal: Journal of personalized medicine

Published: July 09, 2026

CRISPR/Cas9-Mediated Correction of the SLC25A38 Mutation in a Patient With Sideroblastic Anemia.

CRISPR/Cas9-Mediated Correction of the SLC25A38 Mutation in a Patient With Sideroblastic Anemia.

Journal: The journal of gene medicine

Published: June 25, 2026

A Case Report of Pearson Syndrome: Addressing the Complexities beyond Anemia.

A Case Report of Pearson Syndrome: Addressing the Complexities beyond Anemia.

Journal: Molecular syndromology

Published: June 02, 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

Clinical and biochemical footprints of inherited disorders of heme synthesis and porphyrias: Insights from the IEMbase and dyadic nomenclature.

Clinical and biochemical footprints of inherited disorders of heme synthesis and porphyrias: Insights from the IEMbase and dyadic nomenclature.

Journal: Molecular genetics and metabolism

Published: May 21, 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

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

Rethinking the possibilities of adult ring sideroblastic anaemia.

Rethinking the possibilities of adult ring sideroblastic anaemia.

Journal: The Lancet. Haematology

Published: March 17, 2026

Showing 1-12 of 2,260

Last Updated: 11/08/2026