Weifeng Zhang
700 Fengze Street
Quanzhou, 362000, China
Quanzhou, 362000, China
Last Updated: 09/26/2026
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Found 15 publications
Continuous renal replacement therapy for severe transient hyperammonemia in a preterm infant weighing 1120 g: A case report.
Journal: The Journal of international medical research
Published: May 15, 2025
Clinical characteristics and molecular genetic analysis of ten cases of ornithine carbamoyltransferase deficiency in southeastern China.
Journal: Italian journal of pediatrics
Published: November 14, 2023
The efficacy and safety of continuous blood purification in neonates with septic shock and acute kidney injury: a two-center retrospective study.
Journal: European journal of pediatrics
Published: September 19, 2023
Effectiveness and feasibility of continuous renal replacement therapy for acute kidney injury in neonates weighing 3 kg or less: a two-centre, retrospective study.
Journal: BMJ paediatrics open
Published: August 19, 2023
Exploring the diagnostic value of ultrasound radiomics for neonatal respiratory distress syndrome.
Journal: BMC pediatrics
Published: June 12, 2023
Real-life effects, complications, and outcomes in 39 critically ill neonates receiving continuous kidney replacement therapy.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 17, 2022
Case Report: Transient antenatal bartter syndrome in an extremely preterm infant with a novel MAGED2 variant.
Journal: Frontiers in pediatrics
Published: November 08, 2022
Analysis of risk factors for death in 59 cases of critically ill neonates receiving continuous renal replacement therapy: a two-centered retrospective study.
Journal: European journal of pediatrics
Published: September 27, 2022
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.
Journal: Orphanet journal of rare diseases
Published: September 29, 2021
Three Novel and One Potential Hotspot CPT1A Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A Deficiency.
Journal: Frontiers in pediatrics
Published: September 07, 2021
Increased detection of primary carnitine deficiency through second-tier newborn genetic screening.
Journal: Orphanet journal of rare diseases
Published: January 20, 2021
Last Updated: 09/26/2026