Jihong Hao

215#, Heping West Road
Shijiazhuang, 050000, China

Last Updated: 09/26/2026

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Found 22 publications

A Novel TUBB1 p.E158del Variant Causes Inherited Macrothrombocytopenia via Impaired Microtubule Assembly.

A Novel TUBB1 p.E158del Variant Causes Inherited Macrothrombocytopenia via Impaired Microtubule Assembly.

Journal: International journal of laboratory hematology

Published: January 25, 2026

Rare Auer Rods in Vacuole-Like Inclusions in Acute Promyelocytic Leukemia

Rare Auer Rods in Vacuole-Like Inclusions in Acute Promyelocytic Leukemia

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: May 06, 2025

Case Report: A Chinese family with MYH9-RD caused by MYH9 p.E1841K mutation exhibiting widespread may-hegglin inclusions.

Case Report: A Chinese family with MYH9-RD caused by MYH9 p.E1841K mutation exhibiting widespread may-hegglin inclusions.

Journal: Frontiers in pediatrics

Published: March 06, 2025

First reported co-occurrence of Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia with pseudo Chediak-Higashi anomaly and complex karyotype.

First reported co-occurrence of Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia with pseudo Chediak-Higashi anomaly and complex karyotype.

Journal: Clinical chemistry and laboratory medicine

Published: January 22, 2024

Novel compound heterozygous mutations of the NPC1 gene associated with Niemann-pick disease type C: a case report and review of the literature.

Novel compound heterozygous mutations of the NPC1 gene associated with Niemann-pick disease type C: a case report and review of the literature.

Journal: BMC infectious diseases

Published: December 09, 2023

Aleukemic Variant of Mast Cell Leukemia with del (7)(q31): Rare Case Report of an Elderly Chinese Man

Aleukemic Variant of Mast Cell Leukemia with del (7)(q31): Rare Case Report of an Elderly Chinese Man

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: June 14, 2023

“Rod-Like” Cytoplasmic Crystals of Peripheral Lymphocytes in Chronic Lymphocytic Leukemia

“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

Clostridioides difficile infection in infants: a case report and literature review.

Clostridioides difficile infection in infants: a case report and literature review.

Journal: Gut pathogens

Published: February 13, 2023

Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome.

Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome.

Journal: Orphanet journal of rare diseases

Published: May 09, 2022

Erythrophagocytosis of Peripheral Blood Smear in Antiphospholipid Syndrome Associated with B-Cell Lymphoma.

Erythrophagocytosis of Peripheral Blood Smear in Antiphospholipid Syndrome Associated with B-Cell Lymphoma.

Journal: Clinical laboratory

Published: December 15, 2021

Case Report: Wiskott-Aldrich Syndrome Caused by Extremely Skewed X-Chromosome Inactivation in a Chinese Girl.

Case Report: Wiskott-Aldrich Syndrome Caused by Extremely Skewed X-Chromosome Inactivation in a Chinese Girl.

Journal: Frontiers in pediatrics

Published: April 06, 2021

Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family.

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

Showing 1-12 of 22

Last Updated: 09/26/2026