Wang D - Search Results

1

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.

2

Glucose transporter protein syndromes.

De Vivo DC, Wang D, Pascual JM, Ho YY. De Vivo DC, et al. Among authors: wang d. Int Rev Neurobiol. 2002;51:259-88. doi: 10.1016/s0074-7742(02)51008-4. Int Rev Neurobiol. 2002. PMID: 12420362 Review. No abstract available.

3

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.

4

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.

5

Defective glucose transport across brain tissue barriers: a newly recognized neurological syndrome.

Klepper J, Wang D, Fischbarg J, Vera JC, Jarjour IT, O'Driscoll KR, De Vivo DC. Klepper J, et al. Among authors: wang d. Neurochem Res. 1999 Apr;24(4):587-94. doi: 10.1023/a:1022544131826. Neurochem Res. 1999. PMID: 10227690

6

GLUT1-deficiency: barbiturates potentiate haploinsufficiency in vitro.

Klepper J, Fischbarg J, Vera JC, Wang D, De Vivo DC. Klepper J, et al. Among authors: wang d. Pediatr Res. 1999 Dec;46(6):677-83. doi: 10.1203/00006450-199912000-00006. Pediatr Res. 1999. PMID: 10590023

7

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

8

Glucose transporter type 1 deficiency syndrome (Glut1DS): methylxanthines potentiate GLUT1 haploinsufficiency in vitro.

Ho YY, Yang H, Klepper J, Fischbarg J, Wang D, De Vivo DC. Ho YY, et al. Among authors: wang d. Pediatr Res. 2001 Aug;50(2):254-60. doi: 10.1203/00006450-200108000-00015. Pediatr Res. 2001. PMID: 11477212

9

[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.

10

Imaging the metabolic footprint of Glut1 deficiency on the brain.

Pascual JM, Van Heertum RL, Wang D, Engelstad K, De Vivo DC. Pascual JM, et al. Among authors: wang d. Ann Neurol. 2002 Oct;52(4):458-64. doi: 10.1002/ana.10311. Ann Neurol. 2002. PMID: 12325075

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