Ya-nan Hu
Fuzhou, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency.
Journal: Thrombosis journal
Published: August 23, 2022
Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation.
Journal: Frontiers in cardiovascular medicine
Published: March 01, 2022
Retrospective Analysis of the Effect of Lidocaine Combined with Methylprednisolone on Pain Control After Uterine Artery Embolization.
Journal: Frontiers in surgery
Published: February 15, 2022
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.
Journal: Cardiology research and practice
Published: November 16, 2021
A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1.
Journal: Thrombosis journal
Published: July 01, 2021
A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.
Journal: The journal of gene medicine
Published: May 06, 2021
Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.
Journal: BioMed research international
Published: March 18, 2021
Showing 1-8 of 8
Last Updated: 09/26/2026