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  1. No Access

    Article

    Risk stratification of hemodynamically significant patent ductus arteriosus by clinical and genetic factors

    Hemodynamically significant patent ductus arteriosus (hsPDA) is associated with increased comorbidities in neonates. Early evaluation of hsPDA risk is critical to implement individualized intervention. The aim...

    Yu-** Chen, Tian-Tian **ao, Hui-Yao Chen, **ang Chen in World Journal of Pediatrics (2023)

  2. No Access

    Article

    Secondary genomic findings in the 2020 China Neonatal Genomes Project participants

    During next generation sequencing (NGS) data interpretation in critically ill newborns, there is a potential for recognizing and reporting secondary findings (SFs). Early awareness of SFs may provide clues for...

    Hui **ao, Jian-Tao Zhang, **n-Ran Dong, Yu-Lan Lu in World Journal of Pediatrics (2022)

  3. Article

    Open Access

    Human adenovirus (HAdV) infection in children with acute respiratory tract infections in Guangzhou, China, 2010–2021: a molecular epidemiology study

    Human adenovirus (HAdV) infection can cause a variety of diseases. It is a major pathogen of pediatric acute respiratory tract infections (ARIs) and can be life-threatening in younger children. We described th...

    Yi Chen, Tao Lin, Chang-Bing Wang, Wan-Li Liang in World Journal of Pediatrics (2022)

  4. Article

    Application of next generation sequencing in the screening of monogenic diseases in China, 2021: a consensus among Chinese newborn screening experts

    Fan Tong, Jian Wang, Rui **ao, Bing-Bing Wu, Chao-Chun Zou in World Journal of Pediatrics (2022)

  5. No Access

    Article

    Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database

    Primary vesicoureteral reflux (VUR) is a common congenital anomaly of the kidney and urinary tract (CAKUT) in childhood. The present study identified the possible genetic contributions to primary VUR in children.

    Jia-Lu Liu, Qian Shen, Ming-Yan Wu, Guang-Hua Zhu in World Journal of Pediatrics (2021)

  6. No Access

    Article

    Genetic etiologies associated with infantile hydrocephalus in a Chinese infantile cohort

    Infantile hydrocephalus (IHC) is commonly related to other central nervous system diseases, which may have adverse effects on prognosis. The causes of IHC are heterogeneous, and the genetic etiologies are not ...

    Hong-Fang Mei, **n-Ran Dong, Hui-Yao Chen, Yu-Lan Lu in World Journal of Pediatrics (2021)

  7. No Access

    Article

    Identification of eight novel mutations in 11 Chinese patients with maple syrup urine disease

    Maple syrup urine disease (MSUD) is an autosomal recessive inherited disorder that affects the degradation of branched-chain amino acids and is associated with acute and chronic brain dysfunction. This study p...

    Wei-Hua Sun, Bing-Bing Wu, Ya-Qiong Wang, Meng-Yuan Wu in World Journal of Pediatrics (2020)

  8. Article

    Chinese guidelines for the diagnosis and treatment of hand, foot and mouth disease (2018 edition)

    Hand, foot, and mouth disease (HFMD) is a common infectious disease in childhood caused by an enterovirus (EV), and which is principally seen in children under 5 years of age. To promote diagnostic awareness a...

    **ng-Wang Li, **n Ni, Su-Yun Qian, Quan Wang in World Journal of Pediatrics (2018)

  9. No Access

    Article

    Effects of Bifidobacterium supplementation on intestinal microbiota composition and the immune response in healthy infants

    Intestinal microbiotas are thought to be the most important source of maturational stimuli to the development of the immune system. However, few studies have focused on the development of T helper (Th) 1 immun...

    Bing-Bing Wu, Yi Yang, **u Xu, Wei-** Wang in World Journal of Pediatrics (2016)