Lulu Li
Beijing, 100026, China
Last Updated: 09/26/2026
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Found 11 publications
Population-based newborn screening for inherited metabolic diseases in Beijing, China: findings from 404,990 infants.
Journal: Molecular genetics and metabolism
Published: June 25, 2026
Dried blood spot quality in newborn inherited metabolic disease screening in Beijing, 2020-2024: a retrospective analysis of incidence, causes, and improvement strategies.
Journal: BMC pediatrics
Published: April 12, 2026
MassARRAY-based targeted detection of SLC22A5 mutations: A feasibility study for secondary screening of primary carnitine deficiency in newborns.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 15, 2025
Impact of maternal anemia during pregnancy on neonatal metabolic profiles: evidence from the Beijing Birth Cohort Study.
Journal: BMC pregnancy and childbirth
Published: January 21, 2025
Six Chinese patients with propionic acidemia: from asymptomatic to death in the neonatal period.
Journal: Orphanet journal of rare diseases
Published: September 26, 2024
Neonatal Amino Acids and Acylcarnitines Associated With Maternal Blood Glucose Levels Throughout Pregnancy: Insights From the Beijing Birth Cohort Study.
Journal: Diabetes care
Published: January 07, 2024
Clinical characteristics and genetics analysis for the ITD of congenital hypothyroidism.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: January 28, 2022
Derivation of a human induced pluripotent stem cell (hiPSC) line (PUMCSMi001-A) from peripheral blood mononuclear cells of one healthy female donor.
Journal: Stem cell research
Published: March 10, 2021
Novel Gross Deletion Mutations in NTRK1 Gene Associated With Congenital Insensitivity to Pain With Anhidrosis.
Journal: Frontiers in pediatrics
Published: December 05, 2020
Showing 1-11 of 11
Last Updated: 09/26/2026