Zhenzhu Zheng

700 Fengze Street
Quanzhou, 362000, China

Last Updated: 09/26/2026

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Found 28 publications

Upconversion fluorescence immunochromatographic assay for highly sensitive and rapid detection of ovarian function indicators: follicle-stimulating hormone and anti-Müllerian hormone.

Upconversion fluorescence immunochromatographic assay for highly sensitive and rapid detection of ovarian function indicators: follicle-stimulating hormone and anti-Müllerian hormone.

Journal: Analytical methods : advancing methods and applications

Published: July 15, 2025

Large-scale newborn screening for organic acidemias in Quanzhou, China: a 10-year retrospective observational study.

Large-scale newborn screening for organic acidemias in Quanzhou, China: a 10-year retrospective observational study.

Journal: Scientific reports

Published: January 24, 2025

Newborn screening and genetic diagnosis of 3-methylcrotonyl-CoA carboxylase deficiency in Quanzhou,China.

Newborn screening and genetic diagnosis of 3-methylcrotonyl-CoA carboxylase deficiency in Quanzhou,China.

Journal: Molecular genetics and metabolism reports

Published: May 05, 2024

Incorporating Next-Generation Sequencing as a Second-Tier Test for Primary Carnitine Deficiency.

Incorporating Next-Generation Sequencing as a Second-Tier Test for Primary Carnitine Deficiency.

Journal: Molecular genetics & genomic medicine

Published: April 15, 2024

Clinical and genetic analysis of four Chinese patients with holocarboxylase synthetase deficiency and metabolic acidosis.

Clinical and genetic analysis of four Chinese patients with holocarboxylase synthetase deficiency and metabolic acidosis.

Journal: Orphanet journal of rare diseases

Published: February 01, 2024

Newborn screening for primary carnitine deficiency using a second-tier genetic test.

Newborn screening for primary carnitine deficiency using a second-tier genetic test.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: November 16, 2023

Newborn screening for fatty acid oxidation disorders in a southern Chinese population.

Newborn screening for fatty acid oxidation disorders in a southern Chinese population.

Journal: Heliyon

Published: September 03, 2023

Clinical and genetic analysis of 26 Chinese patients with neonatal intrahepatic cholestasis due to citrin deficiency.

Clinical and genetic analysis of 26 Chinese patients with neonatal intrahepatic cholestasis due to citrin deficiency.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: April 25, 2023

Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population.

Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 14, 2022

Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening.

Correction to: Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening.

Journal: Orphanet journal of rare diseases

Published: January 25, 2022

Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening.

Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening.

Journal: Orphanet journal of rare diseases

Published: September 29, 2021

Occurrence of mcr Positive Strains and Molecular Characteristics of Two mcr-1 Positive Salmonella typhimurium and Escherichia coli from a Chinese Women's and Children's Hospital.

Occurrence of mcr Positive Strains and Molecular Characteristics of Two mcr-1 Positive Salmonella typhimurium and Escherichia coli from a Chinese Women's and Children's Hospital.

Journal: Infection and drug resistance

Published: June 02, 2021

Showing 1-12 of 28

Last Updated: 09/26/2026