Wang D - Search Results

1

Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndrome.

Coman DJ, Sinclair KG, Burke CJ, Appleton DB, Pelekanos JT, O'Neil CM, Wallace GB, Bowling FG, Wang D, De Vivo DC, McGill JJ. Coman DJ, et al. Among authors: wang d. J Paediatr Child Health. 2006 May;42(5):263-7. doi: 10.1111/j.1440-1754.2006.00852.x. J Paediatr Child Health. 2006. PMID: 16712556

2

Glucose transporter 1 deficiency syndrome and other glycolytic defects.

De Vivo DC, Leary L, Wang D. De Vivo DC, et al. Among authors: wang d. J Child Neurol. 2002 Dec;17 Suppl 3:3S15-23; discussion 3S24-5. J Child Neurol. 2002. PMID: 12597052 Review.

3

Three Japanese patients with glucose transporter type 1 deficiency syndrome.

Fujii T, Ho YY, Wang D, De Vivo DC, Miyajima T, Wong HY, Tsang PT, Shirasaka Y, Kudo T, Ito M. Fujii T, et al. Among authors: wang d. Brain Dev. 2007 Mar;29(2):92-7. doi: 10.1016/j.braindev.2006.07.007. Epub 2006 Sep 1. Brain Dev. 2007. PMID: 16949238

4

[Type 1 glucose transporter (Glut1) deficiency: manifestations of a hereditary neurological syndrome].

Pascual JM, Lecumberri B, Wang D, Yang R, Engelstad K, De Vivo DC. Pascual JM, et al. Among authors: wang d. Rev Neurol. 2004 May 1-15;38(9):860-4. Rev Neurol. 2004. PMID: 15152356 Free article. Review. Spanish.

5

GLUT1 deficiency and other glucose transporter diseases.

Pascual JM, Wang D, Lecumberri B, Yang H, Mao X, Yang R, De Vivo DC. Pascual JM, et al. Among authors: wang d. Eur J Endocrinol. 2004 May;150(5):627-33. doi: 10.1530/eje.0.1500627. Eur J Endocrinol. 2004. PMID: 15132717 Review.

6

T295M-associated Glut1 deficiency syndrome with normal erythrocyte 3-OMG uptake.

Fujii T, Morimoto M, Yoshioka H, Ho YY, Law PP, Wang D, De Vivo DC. Fujii T, et al. Among authors: wang d. Brain Dev. 2011 Apr;33(4):316-20. doi: 10.1016/j.braindev.2010.06.012. Epub 2010 Jul 13. Brain Dev. 2011. PMID: 20630673

7

Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome.

Klepper J, Garcia-Alvarez M, O'Driscoll KR, Parides MK, Wang D, Ho YY, De Vivo DC. Klepper J, et al. Among authors: wang d. J Clin Lab Anal. 1999;13(3):116-21. doi: 10.1002/(SICI)1098-2825(1999)13:3<116::AID-JCLA5>3.0.CO;2-C. J Clin Lab Anal. 1999. PMID: 10323476 Free PMC article.

8

Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome.

Wang D, Kranz-Eble P, De Vivo DC. Wang D, et al. Hum Mutat. 2000 Sep;16(3):224-31. doi: 10.1002/1098-1004(200009)16:3<224::AID-HUMU5>3.0.CO;2-P. Hum Mutat. 2000. PMID: 10980529

9

Autosomal dominant glut-1 deficiency syndrome and familial epilepsy.

Brockmann K, Wang D, Korenke CG, von Moers A, Ho YY, Pascual JM, Kuang K, Yang H, Ma L, Kranz-Eble P, Fischbarg J, Hanefeld F, De Vivo DC. Brockmann K, et al. Among authors: wang d. Ann Neurol. 2001 Oct;50(4):476-85. doi: 10.1002/ana.1222. Ann Neurol. 2001. PMID: 11603379

10

Glut1 deficiency: CSF glucose. How low is too low?

De Vivo DC, Wang D. De Vivo DC, et al. Among authors: wang d. Rev Neurol (Paris). 2008 Nov;164(11):877-80. doi: 10.1016/j.neurol.2008.10.001. Epub 2008 Nov 5. Rev Neurol (Paris). 2008. PMID: 18990414 No abstract available.

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

63,185 results

Search Page

Filters