Wei XC - Search Results

1

Single-center experience with Beta-propeller protein-associated neurodegeneration (BPAN); expanding the phenotypic spectrum.

Chard M, Appendino JP, Bello-Espinosa LE, Curtis C, Rho JM, Wei XC, Al-Hertani W. Chard M, et al. Among authors: wei xc. Mol Genet Metab Rep. 2019 Jun 19;20:100483. doi: 10.1016/j.ymgmr.2019.100483. eCollection 2019 Sep. Mol Genet Metab Rep. 2019. PMID: 31293896 Free PMC article.

2

Unilateral foot drop as an initial presentation of a brain tumor in a child.

Goia E, Hamilton L, Chan J, Wei XC, Mah JK, Rho JM. Goia E, et al. Among authors: wei xc. J Child Neurol. 2014 Jul;29(7):955-8. doi: 10.1177/0883073813479172. Epub 2013 Mar 1. J Child Neurol. 2014. PMID: 23456535

3

Infraslow EEG changes in infantile spasms.

Myers KA, Bello-Espinosa LE, Wei XC, Scantlebury MH. Myers KA, et al. Among authors: wei xc. J Clin Neurophysiol. 2014 Dec;31(6):600-5. doi: 10.1097/WNP.0000000000000109. J Clin Neurophysiol. 2014. PMID: 25462149

4

"Tinkle Tinkle Little Girl, How We Wonder Why You Can't": An Unusual AIDP-like Syndrome in a Toddler.

Rajapakse T, Hinnell CJ, Wei XC, Mah JK, Rho JM. Rajapakse T, et al. Among authors: wei xc. Can J Neurol Sci. 2015 Jul;42(4):274-7. doi: 10.1017/cjn.2015.42. Epub 2015 May 20. Can J Neurol Sci. 2015. PMID: 25990009 No abstract available.

5

TUBA1A Mutation Associated With Eye Abnormalities in Addition to Brain Malformation.

Myers KA, Bello-Espinosa LE, Kherani A, Wei XC, Innes AM. Myers KA, et al. Among authors: wei xc. Pediatr Neurol. 2015 Nov;53(5):442-4. doi: 10.1016/j.pediatrneurol.2015.07.004. Epub 2015 Jul 22. Pediatr Neurol. 2015. PMID: 26294046

6

Teaching NeuroImages: MRI findings in X-linked adrenoleukodystrophy.

Myers KA, Rho JM, Wei XC. Myers KA, et al. Among authors: wei xc. Neurology. 2015 Oct 27;85(17):e132-3. doi: 10.1212/WNL.0000000000002063. Neurology. 2015. PMID: 26503591 Free PMC article. No abstract available.

7

ALG9-CDG: New clinical case and review of the literature.

Davis K, Webster D, Smith C, Jackson S, Sinasac D, Seargeant L, Wei XC, Ferreira P, Midgley J, Foster Y, Li X, He M, Al-Hertani W. Davis K, et al. Among authors: wei xc. Mol Genet Metab Rep. 2017 Sep 6;13:55-63. doi: 10.1016/j.ymgmr.2017.08.004. eCollection 2017 Dec. Mol Genet Metab Rep. 2017. PMID: 28932688 Free PMC article.

8

Transiently elevated plasma methionine, S-adenosylmethionine and S-adenosylhomocysteine: Unreported laboratory findings in a patient with NGLY1 deficiency, a congenital disorder of deglycosylation.

Chang CA, Wei XC, Martin SR, Sinasac DS, Al-Hertani W. Chang CA, et al. Among authors: wei xc. JIMD Rep. 2019 Jul 22;49(1):21-29. doi: 10.1002/jmd2.12064. eCollection 2019 Sep. JIMD Rep. 2019. PMID: 31497478 Free PMC article.

9

Considering immunologic and genetic evaluation for HLH in neuroinflammation: A case of Griscelli syndrome type 2 with neurological symptoms and a lack of albinism.

Woodward KE, Shah RM, Benseler S, Wei XC, Ng D, Grossman J, Hahn C, Thomas MA, Wright NAM, Appendino JP. Woodward KE, et al. Among authors: wei xc. Pediatr Blood Cancer. 2020 Aug;67(8):e28312. doi: 10.1002/pbc.28312. Epub 2020 May 27. Pediatr Blood Cancer. 2020. PMID: 32459386 No abstract available.

10

MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease.

Kerr M, Hume S, Omar F, Koo D, Barnes H, Khan M, Aman S, Wei XC, Alfuhaid H, McDonald R, McDonald L, Newell C, Sparkes R, Hittel D, Khan A. Kerr M, et al. Among authors: wei xc. Mol Genet Metab. 2020 Sep-Oct;131(1-2):66-82. doi: 10.1016/j.ymgme.2020.08.009. Epub 2020 Sep 18. Mol Genet Metab. 2020. PMID: 32980267

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

199 results

Search Page

Filters