Fu L - Search Results

1

Clinical and Genetic Profile of Chinese Children With Danon Disease: A Single-Center Retrospective Cohort Study.

Zhang Q, Chan W, Chen Y, Wu J, Chen H, Yu T, Yao R, Chen L, Zhang B, Zhang H, Zhang Z, Fu L. Zhang Q, et al. Among authors: fu l. Can J Cardiol. 2024 Oct 11:S0828-282X(24)01018-3. doi: 10.1016/j.cjca.2024.10.005. Online ahead of print. Can J Cardiol. 2024. PMID: 39396772 Free article.

2

Clinical and mutation profile of pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: results from a Chinese cohort.

Chen H, Li X, Liu X, Wang J, Zhang Z, Wu J, Huang M, Guo Y, Li F, Wang X, Fu L. Chen H, et al. Among authors: fu l. Orphanet J Rare Dis. 2019 Feb 7;14(1):29. doi: 10.1186/s13023-019-1010-z. Orphanet J Rare Dis. 2019. PMID: 30732632 Free PMC article.

3

Clinical characteristics and survival of children with hypertrophic cardiomyopathy in China: A multicentre retrospective cohort study.

Chan W, Yang S, Wang J, Tong S, Lin M, Lu P, Yao R, Wu L, Chen L, Guo Y, Shen J, Liu T, Li F, Chen H, Zhang H, Wang S, Fu L. Chan W, et al. Among authors: fu l. EClinicalMedicine. 2022 May 27;49:101466. doi: 10.1016/j.eclinm.2022.101466. eCollection 2022 Jul. EClinicalMedicine. 2022. PMID: 35747179 Free PMC article.

4

Identification of LAMP2 Mutations in Early-Onset Danon Disease With Hypertrophic Cardiomyopathy by Targeted Next-Generation Sequencing.

Fu L, Luo S, Cai S, Hong W, Guo Y, Wu J, Liu T, Zhao C, Li F, Huang H, Huang M, Wang J. Fu L, et al. Am J Cardiol. 2016 Sep 15;118(6):888-894. doi: 10.1016/j.amjcard.2016.06.037. Epub 2016 Jun 27. Am J Cardiol. 2016. PMID: 27460667

5

Catheter ablation of ventricular tachycardia in the pediatric patients: A single-center experience.

Wu J, Chen Y, Ji W, Gu B, Shen J, Fu L, Li F. Wu J, et al. Among authors: fu l. Pacing Clin Electrophysiol. 2020 Jan;43(1):37-46. doi: 10.1111/pace.13835. Epub 2019 Dec 2. Pacing Clin Electrophysiol. 2020. PMID: 31701534

6

Clinical characteristics and therapeutic outcomes of pulmonary arterial hypertension secondary to congenital portosystemic shunts.

Wu J, Lu Y, Zhao W, Shen J, Li F, Zhang H, Chen Q, Fu L. Wu J, et al. Among authors: fu l. Eur J Pediatr. 2021 Mar;180(3):929-936. doi: 10.1007/s00431-020-03817-y. Epub 2020 Oct 3. Eur J Pediatr. 2021. PMID: 33011830

7

A case of non-compaction ventricular myocardium and multiple coronary artery-to-right ventricle fistulae.

Chen Y, Zhang Z, Li F, Fu L, Wu J, Zhang Y, Zhong Y. Chen Y, et al. Among authors: fu l. Int J Cardiol. 2015 Apr 1;184:659-663. doi: 10.1016/j.ijcard.2015.02.042. Epub 2015 Feb 24. Int J Cardiol. 2015. PMID: 25771234 Review. No abstract available.

8

[A case of severe pulmonary hypertension in children treated by transcatheter Potts shunt].

Zhan TL, Chen YW, Wu JJ, Li F, Zhang H, Fu LJ. Zhan TL, et al. Among authors: fu lj. Zhonghua Er Ke Za Zhi. 2023 Feb 2;61(2):169-171. doi: 10.3760/cma.j.cn112140-20220717-00654. Zhonghua Er Ke Za Zhi. 2023. PMID: 36720601 Chinese.

9

Identification of TAZ mutations in pediatric patients with cardiomyopathy by targeted next-generation sequencing in a Chinese cohort.

Wang J, Guo Y, Huang M, Zhang Z, Zhu J, Liu T, Shi L, Li F, Huang H, Fu L. Wang J, et al. Among authors: fu l. Orphanet J Rare Dis. 2017 Feb 10;12(1):26. doi: 10.1186/s13023-016-0562-4. Orphanet J Rare Dis. 2017. PMID: 28183324 Free PMC article.

10

Clinical and Molecular Characterization of Infantile-Onset Pompe Disease in Mainland Chinese Patients: Identification of Two Common Mutations.

Chen X, Liu T, Huang M, Wu J, Zhu J, Guo Y, Xu X, Li F, Wang J, Fu L. Chen X, et al. Among authors: fu l. Genet Test Mol Biomarkers. 2017 Jun;21(6):391-396. doi: 10.1089/gtmb.2016.0424. Epub 2017 Apr 10. Genet Test Mol Biomarkers. 2017. PMID: 28394184

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