Na Tao
China
Last Updated: 09/26/2026
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Found 13 publications
Effects of probiotic supplementation on glycemic control in children with type 1 diabetes: A systematic review and meta-analysis.
Journal: The Journal of international medical research
Published: April 29, 2026
Health Inequities in Older Adults With Type 1 Diabetes: A Nationwide Registry Analysis of Sociodemographic and Clinical Profiles for Glycaemic Control and Complications.
Journal: Diabetes, obesity & metabolism
Published: February 15, 2026
Central Precocious Puberty and Sjogren-Larsson Syndrome in a Child: A Rare Case Report.
Journal: Clinical, cosmetic and investigational dermatology
Published: January 29, 2026
Efficacy and Safety of PEGylated Recombinant Human Growth Hormone in Children With Growth Hormone Deficiency and Idiopathic Short Stature: A Real-World Cohort Study.
Journal: International journal of endocrinology
Published: June 10, 2025
Care, control and complications of hospitalised patients with type 1 diabetes in China: A nationwide-based registry study.
Journal: Diabetes/metabolism research and reviews
Published: December 15, 2023
Establishment and application of a root wounding-immersion method for efficient virus-induced gene silencing in plants.
Journal: Frontiers in plant science
Published: November 11, 2023
DMD mutations in pediatric patients with phenotypes of Duchenne/Becker muscular dystrophy.
Journal: Open medicine (Warsaw, Poland)
Published: July 22, 2022
Gene Polymorphisms Associated with Central Precocious Puberty and Hormone Levels in Chinese Girls.
Journal: International journal of endocrinology
Published: April 26, 2022
Delayed diagnosis of complex glycerol kinase deficiency in a Chinese male infant: a case report.
Journal: BMC pediatrics
Published: August 09, 2021
Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis.
Journal: Pediatric endocrinology, diabetes, and metabolism
Published: February 18, 2021
Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis.
Journal: Pediatric endocrinology, diabetes, and metabolism
Published: November 16, 2020
A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II.
Journal: Molecular genetics & genomic medicine
Published: June 27, 2020
Last Updated: 09/26/2026