Lee WT - Search Results

1

Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency.

Wassenberg T, Molero-Luis M, Jeltsch K, Hoffmann GF, Assmann B, Blau N, Garcia-Cazorla A, Artuch R, Pons R, Pearson TS, Leuzzi V, Mastrangelo M, Pearl PL, Lee WT, Kurian MA, Heales S, Flint L, Verbeek M, Willemsen M, Opladen T. Wassenberg T, et al. Among authors: lee wt. Orphanet J Rare Dis. 2017 Jan 18;12(1):12. doi: 10.1186/s13023-016-0522-z. Orphanet J Rare Dis. 2017. PMID: 28100251 Free PMC article. Review.

2

Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency.

Brun L, Ngu LH, Keng WT, Ch'ng GS, Choy YS, Hwu WL, Lee WT, Willemsen MA, Verbeek MM, Wassenberg T, Régal L, Orcesi S, Tonduti D, Accorsi P, Testard H, Abdenur JE, Tay S, Allen GF, Heales S, Kern I, Kato M, Burlina A, Manegold C, Hoffmann GF, Blau N. Brun L, et al. Among authors: lee wt. Neurology. 2010 Jul 6;75(1):64-71. doi: 10.1212/WNL.0b013e3181e620ae. Epub 2010 May 26. Neurology. 2010. PMID: 20505134

3

Urinary dopamine in aromatic L-amino acid decarboxylase deficiency: the unsolved paradox.

Wassenberg T, Willemsen MA, Geurtz PB, Lammens M, Verrijp K, Wilmer M, Lee WT, Wevers RA, Verbeek MM. Wassenberg T, et al. Among authors: lee wt. Mol Genet Metab. 2010 Dec;101(4):349-56. doi: 10.1016/j.ymgme.2010.08.003. Epub 2010 Aug 14. Mol Genet Metab. 2010. PMID: 20832343

4

Disorders of amino acid metabolism associated with epilepsy.

Lee WT. Lee WT. Brain Dev. 2011 Oct;33(9):745-52. doi: 10.1016/j.braindev.2011.06.014. Epub 2011 Jul 30. Brain Dev. 2011. PMID: 21803516 Review.

5

Aromatic L-amino acid decarboxylase (AADC) is crucial for brain development and motor functions.

Shih DF, Hsiao CD, Min MY, Lai WS, Yang CW, Lee WT, Lee SJ. Shih DF, et al. Among authors: lee sj, lee wt. PLoS One. 2013 Aug 5;8(8):e71741. doi: 10.1371/journal.pone.0071741. Print 2013. PLoS One. 2013. PMID: 23940784 Free PMC article.

6

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. 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.

7

Neuroimaging findings in children with paediatric neurotransmitter diseases.

Lee WT, Weng WC, Peng SF, Tzen KY. Lee WT, et al. 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.

8

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

9

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: lee wt. J Child Neurol. 2010 Dec;25(12):1548-51. doi: 10.1177/0883073810375464. Epub 2010 Jul 20. J Child Neurol. 2010. PMID: 20647579

10

DYT6 Dystonia Mimicking Adolescent Idiopathic Scoliosis Successfully Treated by Pallidal Stimulation.

Tai CH, Lee WT, Tseng SH. Tai CH, et al. Among authors: lee wt. Int Med Case Rep J. 2021 May 13;14:315-321. doi: 10.2147/IMCRJ.S307010. eCollection 2021. Int Med Case Rep J. 2021. PMID: 34012300 Free PMC article.

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