Xianyong Jiang
Beijing, China
Last Updated: 09/26/2026
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Found 14 publications
Case Report: HCV-triggered porphyria cutanea tarda in a patient with SEC23B-mutated congenital dyserythropoietic anemia type II.
Journal: Frontiers in medicine
Published: February 25, 2026
Case Report: Early-onset VEXAS syndrome with recurrent pulmonary inflammation and myelodysplasia: a diagnostic and therapeutic challenge.
Journal: Frontiers in immunology
Published: November 02, 2025
Clinical characteristics and a screening tool for VEXAS syndrome: a case-control study from China.
Journal: Orphanet journal of rare diseases
Published: July 31, 2025
Prognostic Implications of Circulating Plasma Cell Percentage in Multiple Myeloma and Primary Plasma Cell Leukemia Defined by New Criteria.
Journal: Acta haematologica
Published: August 29, 2023
Pure red cell aplasia and minimal residual disease conversion associated with immune reconstitution in a patient with high-risk multiple myeloma.
Journal: Chronic diseases and translational medicine
Published: February 13, 2023
Severe aplastic anemia in a patient with erythropoietic protoporphyria successfully treated by avatrombopag.
Journal: Annals of hematology
Published: September 30, 2021
Distinct Mutation Landscapes Between Acute Myeloid Leukemia With Myelodysplasia-Related Changes and De Novo Acute Myeloid Leukemia.
Journal: American journal of clinical pathology
Published: May 27, 2021
A case report on concurrent occurrence of systemic mastocytosis and myeloid sarcoma presenting with extensive skin involvements and the results of genetic study.
Journal: Medicine
Published: December 17, 2020
Acquired pure red cell aplasia and T cell large granular lymphocytic leukaemia in patients with autoimmune polyglandular syndrome type 1.
Journal: BMC medical genomics
Published: December 01, 2020
Effective treatment of refractory acquired pure red blood cell aplasia with eltrombopag and sirolimus: a case report.
Journal: Therapeutic advances in hematology
Published: March 26, 2020
Analytical evaluation of three soluble transferrin receptor measurement systems for diagnosis of iron deficiency anemia: A retrospective study.
Journal: Journal of clinical laboratory analysis
Published: January 15, 2020
Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis.
Journal: International journal of hematology
Published: October 04, 2016
Last Updated: 09/26/2026