Lee WT - Search Results

1

A novel mutation of ALDH5A1 gene associated with succinic semialdehyde dehydrogenase deficiency.

Lin CY, Weng WC, Lee WT. Lin CY, et al. Among authors: lee wt. J Child Neurol. 2015 Mar;30(4):486-9. doi: 10.1177/0883073814544365. Epub 2014 Sep 22. J Child Neurol. 2015. PMID: 25246302

2

Congenital intracranial teratoma.

Chien YH, Tsao PN, Lee WT, Peng SF, Yau KI. Chien YH, et al. Among authors: lee wt. Pediatr Neurol. 2000 Jan;22(1):72-4. doi: 10.1016/s0887-8994(99)00103-4. Pediatr Neurol. 2000. PMID: 10669211

3

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: lee wt. J Child Neurol. 2004 Jan;19(1):39-42. doi: 10.1177/08830738040190010702. J Child Neurol. 2004. PMID: 15032382

4

Miller-Dieker syndrome associated with tight filum terminale.

Chen SJ, Peng SS, Kuo MF, Lee WT, Liang JS. Chen SJ, et al. Among authors: lee wt. Pediatr Neurol. 2006 Mar;34(3):228-30. doi: 10.1016/j.pediatrneurol.2005.06.017. Pediatr Neurol. 2006. PMID: 16504794

5

Acute disseminated encephalomyelitis in children: one medical center experience.

Weng WC, Peng SS, Lee WT, Fan PC, Chien YH, Du JC, Shen YZ. Weng WC, et al. Among authors: lee wt. Acta Paediatr Taiwan. 2006 Mar-Apr;47(2):67-71. Acta Paediatr Taiwan. 2006. PMID: 16927630

6

Multiple sclerosis with childhood onset: report of 21 cases in Taiwan.

Weng WC, Yang CC, Yu TW, Shen YZ, Lee WT. Weng WC, et al. Among authors: lee wt. Pediatr Neurol. 2006 Nov;35(5):327-34. doi: 10.1016/j.pediatrneurol.2006.05.002. Pediatr Neurol. 2006. PMID: 17074603

7

Clinical analysis of childhood occipital lobe epilepsy in 43 Taiwanese patients.

Du JC, Chien YH, Weng WC, Shen YZ, Lee WT. Du JC, et al. Among authors: lee wt. Pediatr Neurol. 2007 Jun;36(6):387-92. doi: 10.1016/j.pediatrneurol.2007.02.004. Pediatr Neurol. 2007. PMID: 17560500

8

Bronchopulmonary dysplasia predicts adverse developmental and clinical outcomes in very-low-birthweight infants.

Jeng SF, Hsu CH, Tsao PN, Chou HC, Lee WT, Kao HA, Hung HY, Chang JH, Chiu NC, Hsieh WS. Jeng SF, et al. Among authors: lee wt. Dev Med Child Neurol. 2008 Jan;50(1):51-7. doi: 10.1111/j.1469-8749.2007.02011.x. Dev Med Child Neurol. 2008. PMID: 18173631 Free article.

9

Levetiracetam in continuous spike waves during slow-wave sleep syndrome.

Wang SB, Weng WC, Fan PC, Lee WT. Wang SB, et al. Among authors: lee wt. Pediatr Neurol. 2008 Aug;39(2):85-90. doi: 10.1016/j.pediatrneurol.2008.04.007. Pediatr Neurol. 2008. PMID: 18639750 Clinical Trial.

10

Mutation of mitochondrial DNA G13513A presenting with Leigh syndrome, Wolff-Parkinson-White syndrome and cardiomyopathy.

Wang SB, Weng WC, Lee NC, Hwu WL, Fan PC, Lee WT. Wang SB, et al. Among authors: lee nc, lee wt. Pediatr Neonatol. 2008 Aug;49(4):145-9. doi: 10.1016/S1875-9572(08)60030-3. Pediatr Neonatol. 2008. PMID: 19054921 Free article. Review.

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