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2009 | 1 |
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Page 1
Updated Confirmatory Diagnosis for Mucopolysaccharidoses in Taiwanese Infants and the Application of Gene Variants.
Int J Mol Sci. 2022 Sep 1;23(17):9979. doi: 10.3390/ijms23179979.
Int J Mol Sci. 2022.
PMID: 36077388
Free PMC article.
Newborn Screening Program for Mucopolysaccharidosis Type II and Long-Term Follow-Up of the Screen-Positive Subjects in Taiwan.
Lin HY, Chang YH, Lee CL, Tu YR, Lo YT, Hung PW, Niu DM, Liu MY, Liu HY, Chen HJ, Kao SM, Wang LY, Ho HJ, Chuang CK, Lin SP.
Lin HY, et al. Among authors: ho hj.
J Pers Med. 2022 Jun 21;12(7):1023. doi: 10.3390/jpm12071023.
J Pers Med. 2022.
PMID: 35887520
Free PMC article.
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Nationwide Newborn Screening Program for Mucopolysaccharidoses in Taiwan and an Update of the "Gold Standard" Criteria Required to Make a Confirmatory Diagnosis.
Chuang CK, Lee CL, Tu RY, Lo YT, Sisca F, Chang YH, Liu MY, Liu HY, Chen HJ, Kao SM, Wang LY, Ho HJ, Lin HY, Lin SP.
Chuang CK, et al. Among authors: ho hj.
Diagnostics (Basel). 2021 Aug 31;11(9):1583. doi: 10.3390/diagnostics11091583.
Diagnostics (Basel). 2021.
PMID: 34573925
Free PMC article.
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Methylmalonic acidemia/propionic acidemia - the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups.
Chu TH, Chien YH, Lin HY, Liao HC, Ho HJ, Lai CJ, Chiang CC, Lin NC, Yang CF, Hwu WL, Lee NC, Lin SP, Liu CS, Hu RH, Ho MC, Niu DM.
Chu TH, et al. Among authors: ho hj.
Orphanet J Rare Dis. 2019 Apr 2;14(1):73. doi: 10.1186/s13023-019-1045-1.
Orphanet J Rare Dis. 2019.
PMID: 30940196
Free PMC article.
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Enzyme assay and clinical assessment in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4 + 919G→A).
Lin HY, Huang CH, Yu HC, Chong KW, Hsu JH, Lee PC, Cheng KH, Chiang CC, Ho HJ, Lin SP, Chen SJ, Lin PK, Niu DM.
Lin HY, et al. Among authors: ho hj.
J Inherit Metab Dis. 2010 Oct;33(5):619-24. doi: 10.1007/s10545-010-9166-7. Epub 2010 Sep 7.
J Inherit Metab Dis. 2010.
PMID: 20821055
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Newborn screening for methylmalonic aciduria by tandem mass spectrometry: 7 years' experience from two centers in Taiwan.
Cheng KH, Liu MY, Kao CH, Chen YJ, Hsiao KJ, Liu TT, Lin HY, Huang CH, Chiang CC, Ho HJ, Lin SP, Lee NC, Hwu WL, Lin JL, Hung PY, Niu DM.
Cheng KH, et al. Among authors: ho hj.
J Chin Med Assoc. 2010 Jun;73(6):314-8. doi: 10.1016/S1726-4901(10)70067-8.
J Chin Med Assoc. 2010.
PMID: 20603089
Free article.
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High incidence of the cardiac variant of Fabry disease revealed by newborn screening in the Taiwan Chinese population.
Lin HY, Chong KW, Hsu JH, Yu HC, Shih CC, Huang CH, Lin SJ, Chen CH, Chiang CC, Ho HJ, Lee PC, Kao CH, Cheng KH, Hsueh C, Niu DM.
Lin HY, et al. Among authors: ho hj.
Circ Cardiovasc Genet. 2009 Oct;2(5):450-6. doi: 10.1161/CIRCGENETICS.109.862920. Epub 2009 Jul 24.
Circ Cardiovasc Genet. 2009.
PMID: 20031620
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