Wong LJ - Search Results

1

Progressive myopathy with multiple symmetric lipomatosis.

Brunetti-Pierri N, Shaibani A, Zhang S, Wong LJ, Shinawi M. Brunetti-Pierri N, et al. Among authors: wong lj. Arch Neurol. 2009 Dec;66(12):1576-7. doi: 10.1001/archneurol.2009.239. Arch Neurol. 2009. PMID: 20008669 No abstract available.

2

Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.

Shaibani A, Shchelochkov OA, Zhang S, Katsonis P, Lichtarge O, Wong LJ, Shinawi M. Shaibani A, et al. Among authors: wong lj. Arch Neurol. 2009 Aug;66(8):1028-32. doi: 10.1001/archneurol.2009.139. Arch Neurol. 2009. PMID: 19667227 Free PMC article.

3

Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutation.

Shchelochkov O, Wong LJ, Shaibani A, Shinawi M. Shchelochkov O, et al. Among authors: wong lj. Muscle Nerve. 2009 Mar;39(3):374-82. doi: 10.1002/mus.21157. Muscle Nerve. 2009. PMID: 19208414

4

Dilation of the aortic root in mitochondrial disease patients.

Brunetti-Pierri N, Pignatelli R, Fouladi N, Towbin JA, Belmont JW, Craigen WJ, Wong LJ, Jefferies JL, Scaglia F. Brunetti-Pierri N, et al. Among authors: wong lj. Mol Genet Metab. 2011 Jun;103(2):167-70. doi: 10.1016/j.ymgme.2011.02.007. Epub 2011 Feb 18. Mol Genet Metab. 2011. PMID: 21406331

5

Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the FLVCR1 gene.

Shaibani A, Wong LJ, Wei Zhang V, Lewis RA, Shinawi M. Shaibani A, et al. Among authors: wong lj. Int J Neurosci. 2015 Jan;125(1):43-9. doi: 10.3109/00207454.2014.904858. Epub 2014 May 16. Int J Neurosci. 2015. PMID: 24628582

6

Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA depletion.

Zhang S, Li FY, Bass HN, Pursley A, Schmitt ES, Brown BL, Brundage EK, Mardach R, Wong LJ. Zhang S, et al. Among authors: wong lj. Mol Genet Metab. 2010 Jan;99(1):53-7. doi: 10.1016/j.ymgme.2009.09.003. Mol Genet Metab. 2010. PMID: 19815440

7

Mitochondrial disorder with OPA1 mutation lacking optic atrophy.

Milone M, Younge BR, Wang J, Zhang S, Wong LJ. Milone M, et al. Among authors: wong lj. Mitochondrion. 2009 Jul;9(4):279-81. doi: 10.1016/j.mito.2009.03.001. Epub 2009 Mar 20. Mitochondrion. 2009. PMID: 19303950

8

Novel POLG splice site mutation and optic atrophy.

Milone M, Wang J, Liewluck T, Chen LC, Leavitt JA, Wong LJ. Milone M, et al. Among authors: wong lj. Arch Neurol. 2011 Jun;68(6):806-11. doi: 10.1001/archneurol.2011.124. Arch Neurol. 2011. PMID: 21670405

9

Novel (ovario) leukodystrophy related to AARS2 mutations.

Dallabona C, Diodato D, Kevelam SH, Haack TB, Wong LJ, Salomons GS, Baruffini E, Melchionda L, Mariotti C, Strom TM, Meitinger T, Prokisch H, Chapman K, Colley A, Rocha H, Ounap K, Schiffmann R, Salsano E, Savoiardo M, Hamilton EM, Abbink TE, Wolf NI, Ferrero I, Lamperti C, Zeviani M, Vanderver A, Ghezzi D, van der Knaap MS. Dallabona C, et al. Among authors: wong lj. Neurology. 2014 Jun 10;82(23):2063-71. doi: 10.1212/WNL.0000000000000497. Epub 2014 May 7. Neurology. 2014. PMID: 24808023 Free PMC article.

10

Dystrophinopathy mimicking metabolic myopathies.

Liewluck T, Tian X, Wong LJ, Pestronk A. Liewluck T, et al. Among authors: wong lj. Neuromuscul Disord. 2015 Aug;25(8):653-7. doi: 10.1016/j.nmd.2015.04.001. Epub 2015 Apr 11. Neuromuscul Disord. 2015. PMID: 25998609

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