메뉴 건너뛰기




Volumn 25, Issue 12, 2002, Pages 832-837

Primary systemic carnitine deficiency presenting as recurrent Reye-like syndrome and dilated cardiomyopathy

Author keywords

Cardiomyopathy; Carnitine; Reye's syndrome

Indexed keywords

CARNITINE;

EID: 0036990072     PISSN: 02558270     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (9)
  • 1
    • 0026778826 scopus 로고
    • Investigation of metabolic disorders resembling Reye's syndrome
    • Green A, Hall SM. Investigation of metabolic disorders resembling Reye's syndrome. Arch Dis Child 1992;67:1313-7.
    • (1992) Arch Dis Child , vol.67 , pp. 1313-1317
    • Green, A.1    Hall, S.M.2
  • 2
    • 0029744492 scopus 로고    scopus 로고
    • Metabolic function and liver histopathology in Reye-like illnesses
    • Hou JW, Chou SP., Wang TR. Metabolic function and liver histopathology in Reye-like illnesses. Acta Paediatr 1996;85:1053-7.
    • (1996) Acta Paediatr , vol.85 , pp. 1053-1057
    • Hou, J.W.1    Chou, S.P.2    Wang, T.R.3
  • 3
    • 0023488951 scopus 로고
    • New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency
    • Stanley CA. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency. Adv Pediatr 1987;34;59-88.
    • (1987) Adv Pediatr , vol.34 , pp. 59-88
    • Stanley, C.A.1
  • 4
    • 0025101871 scopus 로고
    • Carnitine deficiency syndromes
    • Breningstall GN. Carnitine deficiency syndromes. Pediatr Neurol 1990;6:75-81.
    • (1990) Pediatr Neurol , vol.6 , pp. 75-81
    • Breningstall, G.N.1
  • 6
    • 0021743458 scopus 로고
    • Sodium gradient-stimulated transport of L-carnitine into renal brush border membrane vesicles: Kinetics, specificity, and regulation by dietary carnitine
    • Rebouche CJ, Mack DL. Sodium gradient-stimulated transport of L-carnitine into renal brush border membrane vesicles: kinetics, specificity, and regulation by dietary carnitine. Arch Biochem Biophys 1984;235:393-402.
    • (1984) Arch Biochem Biophys , vol.235 , pp. 393-402
    • Rebouche, C.J.1    Mack, D.L.2
  • 7
    • 0025022129 scopus 로고
    • A genetic defects in carnitine transport causing primary carnitine deficiency
    • Stanley CA, Treem WR, Hale DE, Coates PM. A genetic defects in carnitine transport causing primary carnitine deficiency. Progr Clin Biol Res 1990;321:157-64.
    • (1990) Progr Clin Biol Res , vol.321 , pp. 157-164
    • Stanley, C.A.1    Treem, W.R.2    Hale, D.E.3    Coates, P.M.4
  • 8
    • 0034842137 scopus 로고    scopus 로고
    • Carnitine transport by organic cation transporters and systemic carnitine deficiency
    • Lahjouji K, Mitchell GA, Qureshi IA. Carnitine transport by organic cation transporters and systemic carnitine deficiency. Mol Genet Metab 2001;73:287-97.
    • (2001) Mol Genet Metab , vol.73 , pp. 287-297
    • Lahjouji, K.1    Mitchell, G.A.2    Qureshi, I.A.3
  • 9
    • 0032493741 scopus 로고    scopus 로고
    • Molecular and functional identification of sodium ion dependent, high affinity human carnitine transporter OCTN2
    • Tarnai I, Ohashi R, Nezu J, Yabuchi H, Oku A, Shimane M, Sai Y, Tsuji A. Molecular and functional identification of sodium ion dependent, high affinity human carnitine transporter OCTN2. J Biol Chem 1998;273:20378-82.
    • (1998) J Biol Chem , vol.273 , pp. 20378-20382
    • Tarnai, I.1    Ohashi, R.2    Nezu, J.3    Yabuchi, H.4    Oku, A.5    Shimane, M.6    Sai, Y.7    Tsuji, A.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.