近年发表的部分文章
1. Xiang L, Wang H, Fan S, Zhang W, Lu H, Dong B, Liu S, Chen Y, Wang Y*, Zhao L*, Fu L*. Machine Learning for Early Warning of Septic Shock in Children With Hematological Malignancies Accompanied by Fever or Neutropenia: A Single Center Retrospective Study. Front. Oncol,2021,11:678743.
2. Wu J, Lu Y, Zhao W, Shen J, Li F, Zhang H, Chen Q*, Fu L*. Clinical characteristics and therapeutic outcomes of pulmonary arterial hypertension secondary to congenital portosystemic shunts, Eur J Pediatr, 2021,180(3):929-936.
3. Li X, Yao R, Tan X, Li N, Ding Y, Li J, Chang G, Chen Y, Ma L, Wang J*, Fu L*, Wang X*. Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients.Clin Genet,2019, 96(4):290-299.
4. Chen H, Li X, Liu X, Wang J, Zhang Z, Wu J, Huang M, Guo Y, Li F, Wang X*, Fu L*. Clinical and mutation profile of pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: results from a Chinese cohort, Orphanet J Rare Dis, 2019, 14(1): 29.
5. Wang J, Guo Y, Huang M, Zhang Z, Zhu J, Liu T, Shi L, Li F, Huang H, Fu L*. Identification of TAZ mutations in pediatric patients with cardiomyopathy by targeted next-generation sequencing in a Chinese cohort. Orphanet J Rare Dis, 2017; 12(1):26.
6. Chen X, Liu T, Huang M, Wu J, Zhu J, Guo Y, Xu X, Li F, Wang J*, Fu L*. Clinical and Molecular Characterization of Infantile-Onset Pompe Disease in Mainland Chinese Patients: Identification of Two Common Mutations. Genet Test Mol Biomarkers, 2017, 21(6): 391-396.
7. Fu L#, Luo S#, Cai S, Hong W, Guo Y, Wu J, Liu T, Zhao C, Li F, Huang H, Huang M*, Wang J*. Identification of LAMP2 Mutations in Early-Onset Danon Disease With Hypertrophic Cardiomyopathy by Targeted Next-Generation Sequencing. Am J Cardiol,2016;118(6):888-94.
8. Fu L#, Wang Q#, Wu J, Guo Y, Huang M, Liu T, Chen Q*, Li F*. Congenital extrahepatic portosystemic shunt: an underdiagnosed but treatable cause of hepatopulmonary syndrome. Eur J Pediatr, 2016;175(2):195-201.
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