Ya-Nan Hu

发表

Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation

Jian-Hui Zhang, Jie-wei Luo, Yan-ping Zhang, 2022, Frontiers in Cardiovascular Medicine.

Retrospective Analysis of the Effect of Lidocaine Combined with Methylprednisolone on Pain Control After Uterine Artery Embolization

Jian-Hui Zhang, Yan-ping Zhang, Ya-Nan Hu, 2022, Frontiers in Surgery.

A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency

Dan-dan Ruan, Jie-wei Luo, Fa-qiang Tang, 2021, The journal of gene medicine.

Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A

W. Chen, Dan-dan Ruan, Jian-Hui Zhang, 2022, Cardiology research and practice.

Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant

Dan-dan Ruan, Jie-wei Luo, Fa-qiang Tang, 2022, Frontiers in Pediatrics.

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

X. Yang, Dan-dan Ruan, Jian-Hui Zhang, 2021, BioMed research international.

Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency

Dan-dan Ruan, Jie-wei Luo, Yan-ping Zhang, 2023, Thrombosis Journal.

Clinical and imaging features of six Han patients with SAPHO syndrome

Dan-dan Ruan, Jie-wei Luo, Jia-Bin Wu, 2022, Acta radiologica.

A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1

Jian-Hui Zhang, Jie-wei Luo, Yan-ping Zhang, 2021, Thrombosis Journal.

Han family with essential tremor caused by the P421L variant of the TENM4 gene in China

Jie-wei Luo, Han-Lu Wang, Xing-Lin Ruan, 2023, Neurological Sciences.