Weng WC - Search Results

1

VEGF expression correlates with neuronal differentiation and predicts a favorable prognosis in patients with neuroblastoma.

Weng WC, Lin KH, Wu PY, Ho YH, Liu YL, Wang BJ, Chen CC, Lin YC, Liao YF, Lee WT, Hsu WM, Lee H. Weng WC, et al. Sci Rep. 2017 Sep 11;7(1):11212. doi: 10.1038/s41598-017-11637-8. Sci Rep. 2017. PMID: 28894229 Free PMC article.

2

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. Acta Paediatr Taiwan. 2006 Mar-Apr;47(2):67-71. Acta Paediatr Taiwan. 2006. PMID: 16927630

3

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. Pediatr Neurol. 2006 Nov;35(5):327-34. doi: 10.1016/j.pediatrneurol.2006.05.002. Pediatr Neurol. 2006. PMID: 17074603

4

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: weng wc. Pediatr Neurol. 2007 Jun;36(6):387-92. doi: 10.1016/j.pediatrneurol.2007.02.004. Pediatr Neurol. 2007. PMID: 17560500

5

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

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

6

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: weng wc. Pediatr Neonatol. 2008 Aug;49(4):145-9. doi: 10.1016/S1875-9572(08)60030-3. Pediatr Neonatol. 2008. PMID: 19054921 Free article. Review.

7

Mycoplasma pneumoniae--associated transverse myelitis and rhabdomyolysis.

Weng WC, Peng SS, Wang SB, Chou YT, Lee WT. Weng WC, et al. Pediatr Neurol. 2009 Feb;40(2):128-30. doi: 10.1016/j.pediatrneurol.2008.10.009. Pediatr Neurol. 2009. PMID: 19135630

8

Neuroimaging findings in children with paediatric neurotransmitter diseases.

Lee WT, Weng WC, Peng SF, Tzen KY. Lee WT, et al. Among authors: weng wc. J Inherit Metab Dis. 2009 Jun;32(3):361-70. doi: 10.1007/s10545-009-1106-z. Epub 2009 May 20. J Inherit Metab Dis. 2009. PMID: 19455403 Review.

9

Benign convulsions with mild gastroenteritis: is it associated with sodium channel gene SCN1A mutation?

Weng WC, Hirose S, Lee WT. Weng WC, et al. J Child Neurol. 2010 Dec;25(12):1521-4. doi: 10.1177/0883073810370898. Epub 2010 Jun 2. J Child Neurol. 2010. PMID: 20519669

10

Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosis.

Lin YP, Su YN, Weng WC, Lee WT. Lin YP, et al. Among authors: weng wc. J Child Neurol. 2010 Dec;25(12):1548-51. doi: 10.1177/0883073810375464. Epub 2010 Jul 20. J Child Neurol. 2010. PMID: 20647579

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