De Vivo DC - Search Results

1

Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay.

De Vivo DC, Trifiletti RR, Jacobson RI, Ronen GM, Behmand RA, Harik SI. De Vivo DC, et al. N Engl J Med. 1991 Sep 5;325(10):703-9. doi: 10.1056/NEJM199109053251006. N Engl J Med. 1991. PMID: 1714544 Free article. No abstract available.

2

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: de vivo dc. Ann Neurol. 2002 Oct;52(4):458-64. doi: 10.1002/ana.10311. Ann Neurol. 2002. PMID: 12325075

3

Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy.

Finkel RS, Mercuri E, Darras BT, Connolly AM, Kuntz NL, Kirschner J, Chiriboga CA, Saito K, Servais L, Tizzano E, Topaloglu H, Tulinius M, Montes J, Glanzman AM, Bishop K, Zhong ZJ, Gheuens S, Bennett CF, Schneider E, Farwell W, De Vivo DC; ENDEAR Study Group. Finkel RS, et al. Among authors: de vivo dc. N Engl J Med. 2017 Nov 2;377(18):1723-1732. doi: 10.1056/NEJMoa1702752. N Engl J Med. 2017. PMID: 29091570 Free article. Clinical Trial.

4

Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy.

Mercuri E, Darras BT, Chiriboga CA, Day JW, Campbell C, Connolly AM, Iannaccone ST, Kirschner J, Kuntz NL, Saito K, Shieh PB, Tulinius M, Mazzone ES, Montes J, Bishop KM, Yang Q, Foster R, Gheuens S, Bennett CF, Farwell W, Schneider E, De Vivo DC, Finkel RS; CHERISH Study Group. Mercuri E, et al. Among authors: de vivo dc. N Engl J Med. 2018 Feb 15;378(7):625-635. doi: 10.1056/NEJMoa1710504. N Engl J Med. 2018. PMID: 29443664 Free article. Clinical Trial.

5

Changes in glucose transport and water permeability resulting from the T310I pathogenic mutation in Glut1 are consistent with two transport channels per monomer.

Iserovich P, Wang D, Ma L, Yang H, Zuniga FA, Pascual JM, Kuang K, De Vivo DC, Fischbarg J. Iserovich P, et al. Among authors: de vivo dc. J Biol Chem. 2002 Aug 23;277(34):30991-7. doi: 10.1074/jbc.M202763200. Epub 2002 May 24. J Biol Chem. 2002. PMID: 12032147 Free article.

6

Glucose transporter protein syndromes.

De Vivo DC, Wang D, Pascual JM, Ho YY. De Vivo DC, et al. 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.

7

Glucose transporter 1 deficiency syndrome and other glycolytic defects.

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

8

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: de vivo dc. Eur J Endocrinol. 2004 May;150(5):627-33. doi: 10.1530/eje.0.1500627. Eur J Endocrinol. 2004. PMID: 15132717 Review.

9

Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.

Wang D, Pascual JM, Yang H, Engelstad K, Jhung S, Sun RP, De Vivo DC. Wang D, et al. Among authors: de vivo dc. Ann Neurol. 2005 Jan;57(1):111-8. doi: 10.1002/ana.20331. Ann Neurol. 2005. PMID: 15622525 Clinical Trial.

10

[Progresses in studies on the glucose transporter deficiency syndrome].

Wang D, Sun RP, Wang X, Yang R, Yang H, Pascual JM, De Vivo DC. Wang D, et al. Among authors: de vivo dc. Zhonghua Er Ke Za Zhi. 2004 Oct;42(10):756-8. Zhonghua Er Ke Za Zhi. 2004. PMID: 16221345 Chinese. No abstract available.

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