Yi Liu

Beijing, 100049, China

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications

Stable Isotope Evidence Shows Re-emission of Elemental Mercury Vapor Occurring after Reductive Loss from Foliage.

Stable Isotope Evidence Shows Re-emission of Elemental Mercury Vapor Occurring after Reductive Loss from Foliage.

Journal: Environmental science & technology
Published: December 04, 2018

ZOLEDRONIC ACID VERSUS ALENDRONATE IN THE TREATMENT OF CHILDREN WITH OSTEOGENESIS IMPERFECTA: A 2-YEAR CLINICAL STUDY.

ZOLEDRONIC ACID VERSUS ALENDRONATE IN THE TREATMENT OF CHILDREN WITH OSTEOGENESIS IMPERFECTA: A 2-YEAR CLINICAL STUDY.

Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
Published: February 22, 2018

Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations.

Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 24, 2017

Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI.

Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI.

Journal: Calcified tissue international
Published: August 12, 2016

THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA.

THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA.

Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
Published: August 03, 2016

Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations.

Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: June 13, 2016

Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients.

Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: April 20, 2016

A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta.

A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: April 20, 2016

Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.

Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.

Journal: Journal of human genetics
Published: January 05, 2016

Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta.

Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta.

Journal: Journal of human genetics
Published: November 19, 2015

Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients.

Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients.

Journal: PloS one
Published: April 11, 2014
Showing 1-11 of 11

Last Updated: 09/26/2026