De Vivo DC - Search Results

1

L-carnitine supplementation in childhood epilepsy: current perspectives.

De Vivo DC, Bohan TP, Coulter DL, Dreifuss FE, Greenwood RS, Nordli DR Jr, Shields WD, Stafstrom CE, Tein I. De Vivo DC, et al. Epilepsia. 1998 Nov;39(11):1216-25. doi: 10.1111/j.1528-1157.1998.tb01315.x. Epilepsia. 1998. PMID: 9821988 Free article.

2

The ketogenic diet revisited: back to the future.

Nordli DR Jr, De Vivo DC. Nordli DR Jr, et al. Among authors: de vivo dc. Epilepsia. 1997 Jul;38(7):743-9. doi: 10.1111/j.1528-1157.1997.tb01460.x. Epilepsia. 1997. PMID: 9579900 Free article. Review. No abstract available.

3

Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathy.

Tein I, De Vivo DC, Bierman F, Pulver P, De Meirleir LJ, Cvitanovic-Sojat L, Pagon RA, Bertini E, Dionisi-Vici C, Servidei S, et al. Tein I, et al. Among authors: de vivo dc, de meirleir lj. Pediatr Res. 1990 Sep;28(3):247-55. doi: 10.1203/00006450-199009000-00020. Pediatr Res. 1990. PMID: 2235122 Review.

4

Recurrent childhood myoglobinuria.

Tein I, DiMauro S, DeVivo DC. Tein I, et al. Adv Pediatr. 1990;37:77-117. Adv Pediatr. 1990. PMID: 2264536 Review.

5

Valproic acid impairs carnitine uptake in cultured human skin fibroblasts. An in vitro model for the pathogenesis of valproic acid-associated carnitine deficiency.

Tein I, DiMauro S, Xie ZW, De Vivo DC. Tein I, et al. Among authors: de vivo dc. Pediatr Res. 1993 Sep;34(3):281-7. doi: 10.1203/00006450-199309000-00008. Pediatr Res. 1993. PMID: 8134167

6

Deficient muscle carnitine transport in primary carnitine deficiency.

Pons R, Carrozzo R, Tein I, Walker WF, Addonizio LJ, Rhead W, Miranda AF, Dimauro S, De Vivo DC. Pons R, et al. Among authors: de vivo dc. Pediatr Res. 1997 Nov;42(5):583-7. doi: 10.1203/00006450-199711000-00005. Pediatr Res. 1997. PMID: 9357927

7

Heterozygotes for plasmalemmal carnitine transporter defect are at increased risk for valproic acid-associated impairment of carnitine uptake in cultured human skin fibroblasts.

Tein I, DiMauro S, Xie ZW, De Vivo DC. Tein I, et al. Among authors: de vivo dc. J Inherit Metab Dis. 1995;18(3):313-22. doi: 10.1007/BF00710422. J Inherit Metab Dis. 1995. PMID: 7474898

8

Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.

Tein I, De Vivo DC, Ranucci D, DiMauro S. Tein I, et al. Among authors: de vivo dc. J Inherit Metab Dis. 1993;16(1):135-46. doi: 10.1007/BF00711327. J Inherit Metab Dis. 1993. PMID: 8387612

9

Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.

Tein I, De Vivo DC, Hale DE, Clarke JT, Zinman H, Laxer R, Shore A, DiMauro S. Tein I, et al. Among authors: de vivo dc. Ann Neurol. 1991 Sep;30(3):415-9. doi: 10.1002/ana.410300315. Ann Neurol. 1991. PMID: 1835339

10

The mitochondrial DNA A8344G mutation in Leigh syndrome revealed by analysis in paraffin-embedded sections: revisiting the past.

Santorelli FM, Tanji K, Shanske S, Krishna S, Schmidt RE, Greenwood RS, DiMauro S, De Vivo DC. Santorelli FM, et al. Among authors: de vivo dc. Ann Neurol. 1998 Dec;44(6):962-4. doi: 10.1002/ana.410440616. Ann Neurol. 1998. PMID: 9851442

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