Liang WC - Search Results

1

Combined noninvasive ventilation and mechanical insufflator-exsufflator for acute respiratory failure in patients with neuromuscular disease: effectiveness and outcome predictors.

Chen TH, Liang WC, Chen IC, Liu YC, Hsu JH, Jong YJ. Chen TH, et al. Among authors: liang wc. Ther Adv Respir Dis. 2019 Jan-Dec;13:1753466619875928. doi: 10.1177/1753466619875928. Ther Adv Respir Dis. 2019. PMID: 31544581 Free PMC article.

2

Riboflavin-responsive glutaric aciduria type II with recurrent pancreatitis.

Liang WC, Tsai KB, Lai CL, Chen LH, Jong YJ. Liang WC, et al. Pediatr Neurol. 2004 Sep;31(3):218-21. doi: 10.1016/j.pediatrneurol.2004.02.015. Pediatr Neurol. 2004. PMID: 15351024

3

Diphyllobothriasis latum: the first child case report in Taiwan.

Chou HF, Yen CM, Liang WC, Jong YJ. Chou HF, et al. Among authors: liang wc. Kaohsiung J Med Sci. 2006 Jul;22(7):346-51. doi: 10.1016/S1607-551X(09)70321-3. Kaohsiung J Med Sci. 2006. PMID: 16849103 Free article.

4

Novel LMNA mutation in a Taiwanese family with autosomal dominant Emery-Dreifuss muscular dystrophy.

Liang WC, Yuo CY, Liu CY, Lee CS, Goto K, Hayashi YK, Jong YJ. Liang WC, et al. J Formos Med Assoc. 2007 Feb;106(2 Suppl):S27-31. doi: 10.1016/s0929-6646(09)60349-1. J Formos Med Assoc. 2007. PMID: 17493893 Free article.

5

The effect of hydroxyurea in spinal muscular atrophy cells and patients.

Liang WC, Yuo CY, Chang JG, Chen YC, Chang YF, Wang HY, Ju YH, Chiou SS, Jong YJ. Liang WC, et al. J Neurol Sci. 2008 May 15;268(1-2):87-94. doi: 10.1016/j.jns.2007.11.012. Epub 2007 Dec 31. J Neurol Sci. 2008. PMID: 18166199 Clinical Trial.

6

Clinical and genetic features in a MELAS child with a 3271T>C mutation.

Chou HF, Liang WC, Zhang Q, Goto Y, Jong YJ. Chou HF, et al. Among authors: liang wc. Pediatr Neurol. 2008 Feb;38(2):143-6. doi: 10.1016/j.pediatrneurol.2007.09.015. Pediatr Neurol. 2008. PMID: 18206799

7

ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.

Liang WC, Ohkuma A, Hayashi YK, López LC, Hirano M, Nonaka I, Noguchi S, Chen LH, Jong YJ, Nishino I. Liang WC, et al. Neuromuscul Disord. 2009 Mar;19(3):212-6. doi: 10.1016/j.nmd.2009.01.008. Epub 2009 Feb 26. Neuromuscul Disord. 2009. PMID: 19249206 Free PMC article.

8

High resolution melting analysis facilitates mutation screening of ETFDH gene: applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.

Er TK, Liang WC, Chang JG, Jong YJ. Er TK, et al. Among authors: liang wc. Clin Chim Acta. 2010 May 2;411(9-10):690-9. doi: 10.1016/j.cca.2010.01.033. Epub 2010 Feb 6. Clin Chim Acta. 2010. PMID: 20138856

9

Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy.

Wang CH, Leung M, Liang WC, Hsieh TJ, Chen TH, Jong YJ. Wang CH, et al. Among authors: liang wc. Neuromuscul Disord. 2012 Apr;22(4):331-8. doi: 10.1016/j.nmd.2011.10.018. Epub 2011 Dec 7. Neuromuscul Disord. 2012. PMID: 22153988

10

Intranuclear rods myopathy with autonomic dysfunction.

Chou PC, Liang WC, Nonaka I, Mitsuhashi S, Nishino I, Jong YJ. Chou PC, et al. Among authors: liang wc. Brain Dev. 2013 Aug;35(7):686-9. doi: 10.1016/j.braindev.2012.09.011. Epub 2012 Oct 25. Brain Dev. 2013. PMID: 23102861

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