Xiaoqiang Lian
Handan, China
Last Updated: 09/26/2026
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Found 12 publications
A Novel TUBB1 p.E158del Variant Causes Inherited Macrothrombocytopenia via Impaired Microtubule Assembly.
Journal: International journal of laboratory hematology
Published: January 25, 2026
Combination of selenium and metformin mitigated testicular damage from diabetes mellitus by enhancing glycolysis via AMPK/ SIRT1 pathway.
Journal: Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)
Published: January 12, 2026
Bone Marrow Metastasis from a Pancreatic Neuroendocrine Tumor: Morphologic Mimicry of Acute Leukemia.
Journal: Clinical laboratory
Published: December 09, 2025
Clinical Characteristics and Diagnosis of Children t(8; 21)/AML1-ETO Positive Acute Myeloid Leukemia with Basophilic Granulocytosis.
Journal: Clinical laboratory
Published: November 12, 2025
Clinical Characteristics and Diagnosis of Chronic Myelogenous Leukemia with Rare Karyotype.
Journal: Clinical laboratory
Published: August 08, 2025
“Rod-Like” Cytoplasmic Crystals of Peripheral Lymphocytes in Chronic Lymphocytic Leukemia
Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology
Published: June 06, 2023
Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family.
Journal: Clinical chemistry and laboratory medicine
Published: February 15, 2021
A sporadic MYH9-related disease in a Chinese boy with p.A95T mutation.
Journal: Hematology (Amsterdam, Netherlands)
Published: January 01, 2020
Evans syndrome in a female with erythrophagocytosis by monocytes in peripheral blood smear.
Journal: International journal of laboratory hematology
Published: November 23, 2019
Erythrophagocytosis by Neutrophil and Monocyte in Autoimmune Hemolytic Anemia After Infection.
Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
Published: September 07, 2019
A D1424N mutation in the MYH9 gene results in macrothrombocytopenia and granulocytic inclusion bodies in a Chinese inherited macrothrombocytopenia pedigree.
Journal: Clinical chemistry and laboratory medicine
Published: September 07, 2017
Showing 1-12 of 12
Last Updated: 09/26/2026