Weng WC - Search Results

1

Microstructural changes of brain in patients with aromatic L-amino acid decarboxylase deficiency.

Lee WT, Lin JH, Weng WC, Peng SS. Lee WT, et al. Among authors: weng wc. Hum Brain Mapp. 2017 Mar;38(3):1532-1540. doi: 10.1002/hbm.23470. Epub 2016 Nov 17. Hum Brain Mapp. 2017. PMID: 27859928 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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