Siqi W. Liu
Wenzhou, 325035, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 18 publications
Application of right-opening single flap valvuloplasty based on tubular stomach in gastrointestinal reconstruction after laparoscopic proximal gastrectomy
Journal: Zhonghua wei chang wai ke za zhi = Chinese journal of gastrointestinal surgery
Published: August 24, 2025
Effect of triply periodic minimal surfaces structure and ceramic volume fraction on mechanical properties of polymer-infiltrated ceramic network composites fabricated by additive manufactured zirconia and resin
Journal: Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology
Published: May 30, 2025
Analysis of phenotype and gene mutation in three pedigrees with inherited antithrombin deficiency.
Journal: Journal of clinical laboratory analysis
Published: October 10, 2021
Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: July 15, 2021
Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: November 16, 2020
The diagnosis process of Collet-Sicard syndrome caused by skull base fracture: A case report.
Journal: Neurologia
Published: October 15, 2020
The diagnosis process of Collet-Sicard syndrome caused by skull base fracture: A case report.
Journal: Neurologia
Published: October 15, 2020
Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 14, 2020
Double Heterozygous Mutations (Cys247Tyr and 252delAsn) Cause Factor XII Deficiency in a Chinese Family.
Journal: Hamostaseologie
Published: September 11, 2020
A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: August 25, 2020
Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: August 25, 2020
Last Updated: 09/26/2026