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醫療團隊

專業的醫護人員，提供最佳的醫療服務

醫師介紹

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劉顥筌醫師

先天性心臟病診斷與治療，心房中膈缺損(ASD)與心室中膈缺損(VSD)免開心關閉器置放，開放性動脈導管(PDA)關閉器封堵，肺動脈瓣狹窄(PS)與主動脈瓣狹窄(PS)心導管氣球擴張，主動脈弓窄縮(CoA) 心導管氣球擴張，高血脂的基因檢查評估與治療，兒童心雜音，兒童胸痛或胸悶，川崎症診斷治療與風險評估，心臟超音波心臟結構與功能評估，兒童昏倒，兒童心臟衰竭，兒童高血壓的評估與治療。 疾病基因源頭查找，次世代基因檢查(NGS)結果判讀，疾病精準醫學，基因對於藥物影響評估(藥物基因體學)，遺傳疾病診斷與評估，染色體異常疾病診斷與評估，新陳代謝疾病診斷與治療
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醫師資歷
  • 現職
    • 林口長庚醫院兒童內科部講師級主治醫師
  • 經歷
    • 林口長庚醫院兒童內科部講師級主治醫師
    • 台北榮總員山分院小兒科主治醫師
    • 台北榮總童遺傳內分泌科研究員
    • 台北榮總兒童心臟科研究員
    • 台北榮總兒童醫學部住院醫師，總醫師
  • 學會與認證
    • 台灣兒科專科醫師
    • 中華民國心臟學會兒童心臟專科醫師
    • 中華民國心臟學會兒童心臟專科指導醫師
    • 台灣醫學遺傳學/新陳代謝學次專科醫師
  • 論文及期刊發表
    • Acute sciatica: an unusual presentation of extramedullary relapse of acute lymphoblastic leukemia.
      Int J Hematol. 2007 Aug;86(2):163-5
      Liu HC, Hung GY, Yen HJ, Hsieh MY, Chiou TJ*
    • Various modalities for evaluation of a fused heart in conjoined twins. Pediatr Cardiol. 2012 Jan;33(1):192-200.
      Epub 2011 Oct 15
      Liu HC, Lo CW, Weng ZC, Hwang B, Lee PC*
    • Clinical manifestations vary with different age spectrums in infants with Kawasaki disease. ScientificWorldJournal.
      2012;2012:210382. Epub 2012 Feb 15.
      Liu HC, Lo CW, Hwang B, Lee PC*
    • Effects of enzyme replacement therapy for cardiac-type Fabry patients with a Chinese hotspot late-onset Fabry mutation (IVS4+919G>A).
      BMJ Open. 2013 Jul 16;3(7)
      Lin HT, Liu HC, Huang YH, Liao HC, Hsu TR, Shen CI, Li ST, Li CF, Lee LH, Lee PC, Huang CK, Chiang CC, Lin CY, Lin SP, Niu DM*
    • Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A).
      Clin Chim Acta. 2013 Sep 19;426C:114-120
      Liao HC, Huang YH, Chen YJ, Kao SM, Lin HY, Huang CK, Liu HC, Hsu TR, Lin SP, Yang CF, Fann CS, Chiu PC, Hsieh KS, Fu YC, Ke YY, Lin CY, Tsai FJ, Wang CH, Chao MC, Yu WC, Chiang CC, Niu DM*
    • A large-scale nationwide newborn screening program for Pompe disease in Taiwan: towards effective diagnosis and treatment.
      Am J Med Genet A. 2014 Jan;164(1):54-61
      Yang CF, Liu HC, Hsu TR, Tsai FC, Chiang SF, Chiang CC, Ho HC, Lai CJ, Yang TF, Chuang SY, Lin CY, Niu DM*
    • Clinical observations on enzyme replacement therapy in patients with Fabry disease and the switch from agalsidase beta to agalsidase alfa.
      J Chin Med Assoc. 2013 Dec 30
      Lin HY, Huang YH, Liao HC, Liu HC, Hsu TR, Shen CI, Li ST, Li CF, Lee LH, Lee PC, Huang CK, Chiang CC, Lin SP, Niu DM*.
    • Detecting Multiple Lysosomal Storage Diseases by Tandem Mass Spectrometry- A National Newborn Screening Program in Taiwan.
      Clin Chim Acta. 2014 Feb 7
      Liao HC, Chiang CC, Niu DM, Wang CH, Kao SM, Tsai FJ, Huang YH, Liu HC, Huang CK, Gao HJ, Yang CF, Chan MJ, Lin WD, Chen YJ*.
    • Globotriaosylsphingosine (lyso-Gb3) might not be a reliable marker for monitoring the long-term therapeutic outcomes of enzyme replacement therapy for late-onset Fabry patients with the Chinese hotspot mutation (IVS4+919G>A).
      Orphanet Journal of Rare Diseases. 2014 Jul 22;9(1):111-120.
      Liu HC, Lin HY, Yang CF, Liao HC, Hsu TR, Lo CW, Chang FP, Huang CK, Lu YH, Lin SP, Yu WC, Niu DM*.
    • Endomyocardial biopsies in patients with left ventricular hypertrophy and a common Chinese later-onset Fabry mutation (IVS4+919G>A).
      Orphanet Journal of Rare Diseases. 2014 Jul 1;9:96-107.
      Hsu TR, Sung SH, Chang FP, Yang CF, Liu HC, Lin HY, Huang CK, Gao HJ, Huang YH, Liao HC, Lee PC, Yang AH, Chiang CC, Lin CY, Yu WC, Niu DM*
    • Hepatomegaly and hyperammonemia in a girl with Silver-Russell syndrome caused by maternal uniparental isodisomy of chromosome 7.
      American Journal of Medical Genetics Part A. 2014 Aug;164A(8):2114-7
      Li CF, Lin HY, Liu HC, Lee SH, Lo MY, Lin SP, Lo FS, Niu DM*.
    • High-throughput detection of common sequence variations of Fabry disease in Taiwan using DNA mass spectrometry. Molecular Genetics and Metabolism.
      2014 Apr;111(4):507-12.
      Lee SH, Li CF, Lin HY, Lin CH, Liu HC, Tsai SF, Niu DM
    • Age at First Cardiac Symptoms in Fabry Disease: Association with a Chinese Hotspot Fabry Mutation (IVS4+919G>A), Classical Fabry Mutations, and Sex in a Taiwanese Population from the Fabry Outcome Survey (FOS)
      JIMD Rep. 2015;22:107-13. doi: 10.1007/8904_2015_418. Epub 2015 Mar 12.
      Liu HC, Perrin A, Hsu TR, Yang CF, Lin HY, Yu WC, Niu DM*
    • Clinical observations and treatment of pediatric homozygous familial hypercholesterolemia due to a low-density lipoprotein receptor defect.
      J Clin Lipidol. 2015 Mar-Apr;9(2):234-40. doi: 10.1016/j.jacl.2014.11.011. Epub 2014 Dec 3.
      Huang CH, Chiu PC, Liu HC, Lu YH, Huang JK, Charng MJ, Niu DM*
    • Functional and biological studies of α-galactosidase A variants with uncertain significance from newborn screening in Taiwan.
      Mol Genet Metab. 2017 Jun 8. pii: S1096-7192(17)30141-5.
      Liao HC, Hsu TR, Young L, Chiang CC, Huang CK, Liu HC, Niu DM, Chen YJ*
    • Factors Affecting Psychological and Health-Related Quality-of-Life Status in Children and Adolescents with Congenital Heart Diseases
      Children (Basel). 2022 Apr 18;9(4):578. doi: 10.3390/children9040578
      Liu HC, Chaou CH, Lo CW, Chung HT, Hwang MS.