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我於2001年6月從台大醫學系畢業後即進入台大醫院小兒部接受三年的一般兒科學訓練，取得專科醫師資格後，進一步接受兩年的小兒神經科訓練，並順利取得次專科醫師資格。本人曾於2004年7月至2005年8月任小兒部總醫師，並於2006年7月起升任台大醫院小兒部小兒神經科專任主治醫師負責兒童神經疾病之照護。在教學服務方面，積極加入小兒神經科之教學活動，並且指導年輕醫師的臨床檢查技能。
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本人擔任住院醫師時期在李旺祚醫師的指導下積極從事臨床學術研究，包括兒童多發性硬化症與瀰漫性腦脊髓炎的相關研究，也對兒童發展遲緩、頑性癲癇、中樞神經畸形之相關基因研究加以探討，至今已有多篇學術論文發表於SCI國際醫學期刊，包括Pediatric Neurology以及Acta Paediatrica Taiwanica。因為希望可以進一步從事與臨床相關的基礎研究，故加入動物所神經生物組李心予老師的實驗室，期勉自己將來在神經發育的基礎研究能夠有所發揮。
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| 1. |
Wan KS, Weng WC. Eosinophilic meningitis in a child raising snails as pets. Acta Trop. 2004 Mar;90(1):51-3. |
| 2. |
Weng WC, Peng SS, Lee WT, Fan PC, Chien YH, Du JC, Shen YZ. Acute disseminated encephalomyelitis in children: one medical center experience. Acta Paediatr Taiwan. 2006 Mar-Apr;47(2):67-71 |
| 3. |
Weng WC, Yang CC, Yu TW, Shen YZ, Lee WT. Multiple sclerosis with childhood onset: report of 21 cases in Taiwan. Pediatr Neurol. 2006 Nov;35(5):327-34. |
| .4. |
Du JC, Chien YH, Weng WC, Shen YZ, Lee WT. Clinical analysis of childhood occipital lobe epilepsy in 43 Taiwanese patients. Pediatr Neurol. 2007 Jun;36(6):387-92.. |
| 5. |
Wang SB, Weng WC, Fan PC, Lee WT. Levetiracetam in continuous spike waves during slow-wave sleep syndrome. Pediatr Neurol. 2008 Aug;39(2):85-90. |
| 6. |
Wang SB, Weng WC, Lee NC, Hwu WL, Fan PC, Lee WT. Mutation of mitochondrial DNA G13513A presenting with Leigh syndrome, Wolff-Parkinson-White syndrome and cardiomyopathy. Pediatr neonatol. 2008 Aug;49(4):145-9. |
| 7. |
Weng WC, Peng SS, Wang SB, Chou YT, Lee WT. Mycoplasma pneumoniae-Associated Transverse Myelitis and Rhabdomyolysis. Pediatr Neurol. 2009 Feb;40(2):128-30. |
| 8. |
Lee WT, Weng WC, Peng SF, Tzen KY. Neuroimaging findings in children with paediatric neurotransmitter diseases. J Inherit Metab Dis. 2009 Jun;32(3): 361- 70
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| 9. |
Weng WC, Hirose S, Lee WT. Benign convulsions with mild gastroenteritis: is it associated with sodium channel gene SCN1A mutation? J Child Neurol. 2010 Jun 2. |
| 10. |
Lin YP, Ni YH, Weng WC*, Lee WT. Cyclic vomiting syndrome and migraine in children: a single-center experience. J Formos Med Assoc. 2010 (accepted) (Corresponding) |
| 11. |
Lin YP, Su YN, Weng WC*, Lee WT. Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosis. J Child Neurol. 2010 July 20. (Corresponding) |
| 12. |
Chen MY, Liu HM, Weng WC, Peng SF, Wu ET, Chiu SN. Neonate with severe heart failure related to vein of Galen malformation. Pediatr Neonatol. 2010 Aug;51(4):245-8. |
| 13. |
Weng WC, Peng SS, Lee WT. Acute necrotizing encephalopathy of childhood with spinal cord involvement: Report of one case. J Child Neurol. 2010 Sep 7.
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| 14. |
Kao YC, Peng SS, Weng WC, Lin MI, Lee WT. Evaluation of White Matter Changes in Agyria-Pachygyria Complex Using Diffusion Tensor Imaging. J Child Neurol. 2010 Oct 6. |
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