Hsueh HW - Search Results

1

The diversity of hereditary neuromuscular diseases: Experiences from molecular diagnosis.

Hsueh HW, Weng WC, Fan PC, Chien YH, Yang FJ, Lee WT, Lin RJ, Hwu WL, Yang CC, Lee NC. Hsueh HW, et al. J Formos Med Assoc. 2022 Dec;121(12):2574-2583. doi: 10.1016/j.jfma.2022.06.012. Epub 2022 Jul 9. J Formos Med Assoc. 2022. PMID: 35821219 Free article.

2

Guillain-Barré Syndrome with extreme hypertension: A case report.

Liao CW, Hsueh HW, Chao CC. Liao CW, et al. Among authors: hsueh hw. J Formos Med Assoc. 2019 Dec;118(12):1674-1675. doi: 10.1016/j.jfma.2019.08.013. Epub 2019 Aug 30. J Formos Med Assoc. 2019. PMID: 31477485 Free article. No abstract available.

3

Predictors and associating factors of nasogastric tube removal: Clinical and brain imaging data analysis in post-stroke dysphagia.

Hsueh HW, Chen YC, Chang CF, Wang TG, Chiu MJ. Hsueh HW, et al. J Formos Med Assoc. 2020 Dec;119(12):1862-1870. doi: 10.1016/j.jfma.2020.02.015. Epub 2020 Mar 18. J Formos Med Assoc. 2020. PMID: 32199716 Free article.

4

Autosomal dominant cerebellar ataxia, deafness, and narcolepsy with amenorrhea, subclinical optic atrophy, and electroencephalographic abnormality: A case report.

Chang KC, Kuo YC, Hsueh HW, Lee NC, Yang CC, Hsieh ST, Chao CC. Chang KC, et al. Among authors: hsueh hw. eNeurologicalSci. 2020 Sep 9;21:100271. doi: 10.1016/j.ensci.2020.100271. eCollection 2020 Dec. eNeurologicalSci. 2020. PMID: 32984563 Free PMC article. No abstract available.

5

A systematic review of late-onset and very-late-onset multiple acyl-coenzyme A dehydrogenase deficiency: Cohort analysis and patient report from Taiwan.

Kuo YC, Hsueh HW, Hsueh SJ, Lee NC, Hsieh MJ, Chao CC, Chien YH, Huang PH, Yang CC. Kuo YC, et al. Among authors: hsueh sj, hsueh hw. Neuromuscul Disord. 2021 Mar;31(3):218-225. doi: 10.1016/j.nmd.2021.01.006. Epub 2021 Jan 13. Neuromuscul Disord. 2021. PMID: 33589341

6

Lactate peak in muscle disclosed by magnetic resonance spectroscopy in a patient with CPEO-plus syndrome.

Fan SP, Hsueh HW, Huang HC, Chang K, Lee NC, Huang PH, Yang CC. Fan SP, et al. Among authors: hsueh hw. eNeurologicalSci. 2021 Jul 23;24:100360. doi: 10.1016/j.ensci.2021.100360. eCollection 2021 Sep. eNeurologicalSci. 2021. PMID: 34377843 Free PMC article.

7

Thymidine Kinase 2 Deficiency-Induced Adult-Onset Ptosis and Proximal Weakness.

Cheng CY, Chang KC, Hsueh HW, Lee NC, Huang PH, Yang CC, Hwu WL, Hsieh ST, Chao CC. Cheng CY, et al. Among authors: hsueh hw. Neurol Clin Pract. 2021 Jun;11(3):e379-e382. doi: 10.1212/CPJ.0000000000000850. Neurol Clin Pract. 2021. PMID: 34484922 Free PMC article. No abstract available.

8

Diagnostic Challenges of Neuromuscular Disorders after Whole Exome Sequencing.

Chen PS, Chao CC, Tsai LK, Huang HY, Chien YH, Huang PH, Hwu WL, Hsieh ST, Lee NC, Hsueh HW, Yang CC. Chen PS, et al. Among authors: hsueh hw. J Neuromuscul Dis. 2023;10(4):667-684. doi: 10.3233/JND-230013. J Neuromuscul Dis. 2023. PMID: 37066920 Free PMC article.

9

Identification of an 85-kb Heterozygous 4p Microdeletion With Full Genome Analysis in Autosomal Dominant Charcot-Marie-Tooth Disease.

Hsueh HW, Kao HJ, Chao CC, Hsueh SJ, Huang YN, Lin WJ, Su JP, Shy HT, Yeh TY, Lin CC, Kwok PY, Lee NC, Hsieh ST. Hsueh HW, et al. Neurol Genet. 2023 Jun 16;9(4):e200078. doi: 10.1212/NXG.0000000000200078. eCollection 2023 Aug. Neurol Genet. 2023. PMID: 37346931 Free PMC article.

10

Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5.

Chen PS, Lee NC, Sung CJ, Liu YW, Weng WC, Fan PC, Lee WT, Chien YH, Wu CS, Sung YF, Tsai MC, Lee YC, Hsueh HW, Fan SM, Wu MC, Li H, Chen HY, Lin HI, Ou-Yang CH, Hwuh WL, Lin CH. Chen PS, et al. Among authors: hsueh hw. Mov Disord. 2023 Dec;38(12):2217-2229. doi: 10.1002/mds.29604. Epub 2023 Sep 27. Mov Disord. 2023. PMID: 37752895

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