Hsu CC - Search Results

1

Poor outcome for neonatal-type nonketotic hyperglycinemia treated with high-dose sodium benzoate and dextromethorphan.

Chien YH, Hsu CC, Huang A, Chou SP, Lu FL, Lee WT, Hwu WL. Chien YH, et al. Among authors: hsu cc. J Child Neurol. 2004 Jan;19(1):39-42. doi: 10.1177/08830738040190010702. J Child Neurol. 2004. PMID: 15032382

2

Enzyme replacement therapy with imiglucerase in Taiwanese patients with type I Gaucher disease.

Hsu CC, Chien YH, Lai MY, Hwu WL. Hsu CC, et al. J Formos Med Assoc. 2002 Sep;101(9):627-31. J Formos Med Assoc. 2002. PMID: 12645190 Clinical Trial.

3

Distal arthrogryposis in two sisters born to different fathers.

Hwu WL, Chien YH, Hsu CC. Hwu WL, et al. Among authors: hsu cc. Am J Med Genet A. 2004 Feb 15;125A(1):100-1. doi: 10.1002/ajmg.a.20451. Am J Med Genet A. 2004. PMID: 14755476 No abstract available.

4

Two frequent mutations associated with the classic form of propionic acidemia in Taiwan.

Chiu YH, Liu YN, Liao WL, Chang YC, Lin SP, Hsu CC, Chiu PC, Niu DM, Wang CH, Ke YY, Chien YH, Hsiao KJ, Liu TT. Chiu YH, et al. Among authors: hsu cc. Biochem Genet. 2014 Oct;52(9-10):415-29. doi: 10.1007/s10528-014-9657-6. Epub 2014 May 27. Biochem Genet. 2014. PMID: 24863100

5

Long-term effects of enzyme replacement therapy for Taiwanese patients with mucopolysaccharidosis IVA.

Lin HY, Chuang CK, Ke YY, Hsu CC, Chiu PC, Niu DM, Tsai FJ, Hwu WL, Lin JL, Lin SP. Lin HY, et al. Among authors: hsu cc. Pediatr Neonatol. 2019 Jun;60(3):342-343. doi: 10.1016/j.pedneo.2018.08.005. Epub 2018 Aug 23. Pediatr Neonatol. 2019. PMID: 30241882 Free article. No abstract available.

6

Cardiac manifestations and gene mutations of patients with RASopathies in Taiwan.

Lee CL, Tan LTH, Lin HY, Hwu WL, Lee NC, Chien YH, Chuang CK, Wu MH, Wang JK, Chu SY, Lin JL, Lo FS, Su PH, Hsu CC, Ko YY, Chen MR, Chiu HC, Lin SP. Lee CL, et al. Among authors: hsu cc. Am J Med Genet A. 2020 Feb;182(2):357-364. doi: 10.1002/ajmg.a.61429. Epub 2019 Dec 14. Am J Med Genet A. 2020. PMID: 31837205

7

Genotype-Phenotype Dissociation in Two Taiwanese Children with Molybdenum Cofactor Deficiency Caused by MOCS2 Mutation.

Lee HF, Hsu CC, Chi CS, Tsai CR. Lee HF, et al. Among authors: hsu cc. Neuropediatrics. 2022 Jun;53(3):200-203. doi: 10.1055/s-0041-1736181. Epub 2021 Oct 21. Neuropediatrics. 2022. PMID: 34674206

8

Omphalocele and gastroschisis in Taiwan.

Hsu CC, Lin SP, Chen CH, Chi CS, Lee HC, Hung HY, Kao HA, Hsu CH. Hsu CC, et al. Among authors: hsu ch. Eur J Pediatr. 2002 Oct;161(10):552-5. doi: 10.1007/s00431-002-1031-8. Epub 2002 Aug 15. Eur J Pediatr. 2002. PMID: 12297903

9

Association of Methylenetetrahydrofolate Reductase rs1801133 Polymorphism with osteoporosis and fracture risk in Taiwan.

Li MH, Chen IC, Yang HW, Yen HC, Ke YY, Chen YM, Hsu CC. Li MH, et al. Among authors: hsu cc. Int J Med Sci. 2024 Aug 19;21(12):2261-2271. doi: 10.7150/ijms.97524. eCollection 2024. Int J Med Sci. 2024. PMID: 39310265 Free PMC article.

10

The influence of neonatal intensive care unit design on sound level.

Chen HL, Chen CH, Wu CC, Huang HJ, Wang TM, Hsu CC. Chen HL, et al. Among authors: hsu cc. Pediatr Neonatol. 2009 Dec;50(6):270-4. doi: 10.1016/S1875-9572(09)60076-0. Pediatr Neonatol. 2009. PMID: 20025140 Free article.

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