Wanzhong Z. Kong

Wenzhou, 325000, China

Last Updated: 09/26/2026

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Found 13 publications

Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes

Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: March 16, 2026

The simplified agar dilution method (SAD) for simple and accurate fosfomycin MIC testing of urinary Escherichia coli isolates.

The simplified agar dilution method (SAD) for simple and accurate fosfomycin MIC testing of urinary Escherichia coli isolates.

Journal: Journal of microbiological methods

Published: January 26, 2026

Variable clinical features and delayed diagnosis in six Chinese patients with anti-interferon-gamma autoantibodies: a retrospective analysis in a university hospital in China.

Variable clinical features and delayed diagnosis in six Chinese patients with anti-interferon-gamma autoantibodies: a retrospective analysis in a university hospital in China.

Journal: BMC immunology

Published: June 11, 2025

Analysis of the Phenotype and Gene Mutations of Two Families With Combined Mutations of Anticoagulant Protein Genes.

Analysis of the Phenotype and Gene Mutations of Two Families With Combined Mutations of Anticoagulant Protein Genes.

Journal: Molecular genetics & genomic medicine

Published: April 29, 2025

NBEAL2 gene mutations do not always lead to gray platelet syndrome: A case report.

NBEAL2 gene mutations do not always lead to gray platelet syndrome: A case report.

Journal: Medicine

Published: October 28, 2024

Three simple and cost-effective assays for AAC(6')-Ib-cr enzyme activity.

Three simple and cost-effective assays for AAC(6')-Ib-cr enzyme activity.

Journal: Frontiers in microbiology

Published: October 18, 2024

Various clinical manifestations of 223 patients with IgE deficiency in a tertiary hospital in China: A cross-sectional study.

Various clinical manifestations of 223 patients with IgE deficiency in a tertiary hospital in China: A cross-sectional study.

Journal: Medicine

Published: June 14, 2024

Analysis of a pedigree with inherited factor V deficiency caused by compound heterozygous mutation

Analysis of a pedigree with inherited factor V deficiency caused by compound heterozygous mutation

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: April 15, 2021

The abnormal distribution of NK cell subsets before HAART treatment may be related to the level of immune reconstitution in HIV patient.

The abnormal distribution of NK cell subsets before HAART treatment may be related to the level of immune reconstitution in HIV patient.

Journal: International immunopharmacology

Published: February 08, 2021

The epidemiology and clinical feature of selective immunoglobulin a deficiency of Zhejiang Province in China.

The epidemiology and clinical feature of selective immunoglobulin a deficiency of Zhejiang Province in China.

Journal: Journal of clinical laboratory analysis

Published: January 15, 2020

Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation.

Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation.

Journal: The Journal of biological chemistry

Published: August 09, 2019

Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript.

Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript.

Journal: Nucleic acids research

Published: February 02, 2019

Showing 1-12 of 13

Last Updated: 09/26/2026