Tein I - Search Results

1

Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.

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

2

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. Pediatr Res. 1990 Sep;28(3):247-55. doi: 10.1203/00006450-199009000-00020. Pediatr Res. 1990. PMID: 2235122 Review.

3

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. J Inherit Metab Dis. 1995;18(3):313-22. doi: 10.1007/BF00710422. J Inherit Metab Dis. 1995. PMID: 7474898

4

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. Pediatr Res. 1993 Sep;34(3):281-7. doi: 10.1203/00006450-199309000-00008. Pediatr Res. 1993. PMID: 8134167

5

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. Ann Neurol. 1991 Sep;30(3):415-9. doi: 10.1002/ana.410300315. Ann Neurol. 1991. PMID: 1835339

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: tein i. Pediatr Res. 1997 Nov;42(5):583-7. doi: 10.1203/00006450-199711000-00005. Pediatr Res. 1997. PMID: 9357927

7

Clinical and biochemical heterogeneity in an Italian family with CPT II deficiency due to Ser 113 Leu mutation.

Rafay MF, Murphy EG, McGarry JD, Kaufmann P, DiMauro S, Tein I. Rafay MF, et al. Among authors: tein i. Can J Neurol Sci. 2005 Aug;32(3):316-20. doi: 10.1017/s0317167100004194. Can J Neurol Sci. 2005. PMID: 16225172

8

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.

9

Glucose-free medium exacerbates microvesicular steatosis in cultured skin fibroblasts of genetic defects of fatty acid oxidation. A novel screening test.

Renaud DL, Edwards V, Wilson GJ, Tein I. Renaud DL, et al. Among authors: tein i. J Inherit Metab Dis. 2002 Nov;25(7):547-55. doi: 10.1023/a:1022039206660. J Inherit Metab Dis. 2002. PMID: 12638938

10

Reversal of valproic acid-associated impairment of carnitine uptake in cultured human skin fibroblasts.

Tein I, Xie ZW. Tein I, et al. Biochem Biophys Res Commun. 1994 Oct 28;204(2):753-8. doi: 10.1006/bbrc.1994.2523. Biochem Biophys Res Commun. 1994. PMID: 7980539

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