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Volumn 48, Issue 2, 2012, Pages 75-81

Refined staging for chorioretinopathy in long-chain 3-hydroxyacyl coenzyme a dehydrogenase deficiency

Author keywords

Fatty acid oxidation; Inherited metabolic disorder; Pigmentary retinopathy, classification

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; LONG CHAIN 3 HYDROXYACYL COENZYME A DEHYDROGENASE; UNCLASSIFIED DRUG;

EID: 84859141326     PISSN: 00303747     EISSN: 14230259     Source Type: Journal    
DOI: 10.1159/000334874     Document Type: Article
Times cited : (14)

References (8)
  • 1
    • 0031956979 scopus 로고    scopus 로고
    • Ophthalmo-logic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation. A new type of hereditary metabolic chorioretinopathy
    • 82
    • Tyni T, Kivelä T, Lappi M, et al: Ophthalmo-logic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation. A new type of hereditary metabolic chorioretinopathy. Ophthalmology 1998; 105: 810-82 4.
    • (1998) Ophthalmology , vol.105 , Issue.810 , pp. 4
    • Tyni, T.1    Kivelä, T.2    Lappi, M.3
  • 3
    • 0028597508 scopus 로고
    • Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein
    • Ijlst L, Wanders RJA, Ushikubo S, et al: Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein. Biochim Biophys Acta 1994; 1215: 347-350.
    • (1994) Biochim Biophys Acta , vol.1215 , pp. 347-350
    • Ijlst, L.1    Wanders, R.J.A.2    Ushikubo, S.3
  • 5
    • 0031808147 scopus 로고    scopus 로고
    • Ophthalmic pathology in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation
    • DOI 10.1076/ceyr.17.6.551.5182
    • Tyni T, Pihko H, Kivelä T: Ophthalmic pathology in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation. Curr Eye Res 1998; 17: 551-559. (Pubitemid 28288653)
    • (1998) Current Eye Research , vol.17 , Issue.6 , pp. 551-559
    • Tyni, T.1    Pinko, H.2    Kivela, T.3
  • 7
    • 45849118041 scopus 로고    scopus 로고
    • Plus disease in retinopathy of prematurity: An analysis of diagnostic performance
    • Chiang MF, Gelman R, Jiang L, et al: Plus disease in retinopathy of prematurity: an analysis of diagnostic performance. Trans Am Ophthalmol Soc 2007; 105:73-85.
    • (2007) Trans Am Ophthalmol Soc , vol.105 , pp. 73-85
    • Chiang, M.F.1    Gelman, R.2    Jiang, L.3
  • 8
    • 36549002810 scopus 로고    scopus 로고
    • Evaluation of a computer-based system for plus-disease diagnosis in retinopathy of prematurit y
    • Koreen S, Gelman R, Martinez-Perez ME, et al: Evaluation of a computer-based system for plus-disease diagnosis in retinopathy of prematurit y. Opht halmolog y 2007; 114: 59-67.
    • (2007) Opht Halmolog y , vol.114 , pp. 59-67
    • Koreen, S.1    Gelman, R.2    Martinez-Perez, M.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.