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Volumn 41, Issue 11, 1997, Pages 1137-1139

Depressive disorder due to mitochondrial transfer RNA(Leu(UUR)) mutation

Author keywords

coenzyme Q10; Depressive disorder; idebenone; mitochondrial cytopathy

Indexed keywords

IDEBENONE; MITOCHONDRIAL DNA; MITOCHONDRIAL RNA; TRANSFER RNA; UBIQUINONE;

EID: 0030907493     PISSN: 00063223     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3223(97)00005-X     Document Type: Article
Times cited : (42)

References (20)
  • 1
    • 0026707293 scopus 로고
    • Single photon emission tomography with 99m-Tc-exametazine in major depression and the pattern of brain activity underlying the psychotic/neurotic continuum
    • Austin M-P, Dougall N, Ross M, Murray C, O'Carroll RE, Moffoot A, et al (1992): Single photon emission tomography with 99m-Tc-exametazine in major depression and the pattern of brain activity underlying the psychotic/neurotic continuum. J Affect Disord 26:31-44.
    • (1992) J Affect Disord , vol.26 , pp. 31-44
    • Austin, M.-P.1    Dougall, N.2    Ross, M.3    Murray, C.4    O'Carroll, R.E.5    Moffoot, A.6
  • 4
    • 0025666322 scopus 로고
    • A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
    • Goto Y, Nonka I, Horai S (1990): A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 348:651-653.
    • (1990) Nature , vol.348 , pp. 651-653
    • Goto, Y.1    Nonka, I.2    Horai, S.3
  • 6
    • 0029834971 scopus 로고    scopus 로고
    • Idebenone improves cerebral mitochondrial oxidative metabolism in a patient with MELAS
    • Ikejiri Y, Mori E, Ishii K, Nishimoto K, Yasuda M, Sasaki M (1996): Idebenone improves cerebral mitochondrial oxidative metabolism in a patient with MELAS. Neurology 47:583-585.
    • (1996) Neurology , vol.47 , pp. 583-585
    • Ikejiri, Y.1    Mori, E.2    Ishii, K.3    Nishimoto, K.4    Yasuda, M.5    Sasaki, M.6
  • 7
    • 0025055049 scopus 로고
    • A case of mitochondrial myopathy, encephalopathy and lactic acidosis due to cytochrome c oxidase deficiency with neurologic muscular changes
    • Jinnai K, Yamada H, Kanda F, Masui Y, Tanaka M, Ozawa T, et al (1990): A case of mitochondrial myopathy, encephalopathy and lactic acidosis due to cytochrome c oxidase deficiency with neurologic muscular changes. Eur Neurol 30:56-60.
    • (1990) Eur Neurol , vol.30 , pp. 56-60
    • Jinnai, K.1    Yamada, H.2    Kanda, F.3    Masui, Y.4    Tanaka, M.5    Ozawa, T.6
  • 8
    • 0029978356 scopus 로고
    • Deletion of leukocyte mitochondrial DNA in bipolar disorder
    • Kato T, Takahashi Y (1995): Deletion of leukocyte mitochondrial DNA in bipolar disorder. J Affect Disord 37:67-73.
    • (1995) J Affect Disord , vol.37 , pp. 67-73
    • Kato, T.1    Takahashi, Y.2
  • 12
    • 0026566806 scopus 로고
    • Central nervous system changes in mitochondrial encephalomyopathy: Light and electron microscopic study
    • Mizukami K, Sasaki M, Suzuki T, Shirahashi H, Koizumi J, Ohkoshi N, et al (1992): Central nervous system changes in mitochondrial encephalomyopathy: Light and electron microscopic study. Acta Neuropathol 83:449-452.
    • (1992) Acta Neuropathol , vol.83 , pp. 449-452
    • Mizukami, K.1    Sasaki, M.2    Suzuki, T.3    Shirahashi, H.4    Koizumi, J.5    Ohkoshi, N.6
  • 13
    • 0024459681 scopus 로고
    • 123I) iodoamphetamine in two cases with mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS)
    • 123I) iodoamphetamine in two cases with mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS). Neuroradiology 31:358-361.
    • (1989) Neuroradiology , vol.31 , pp. 358-361
    • Morita, K.1    Ono, S.2    Fukunaga, M.3    Yasuda, T.4    Higashi, Y.5    Terao, A.6
  • 14
    • 0029130640 scopus 로고
    • Decreased cerebral blood perfusion with an A-to-G mutation in the mitochondrial gene: A possible contribution to cognition deficits in diabetes mellitus
    • Odawara M, Tada K, Yamashita K (1995): Decreased cerebral blood perfusion with an A-to-G mutation in the mitochondrial gene: A possible contribution to cognition deficits in diabetes mellitus. Diabetologia 38:1004-1005.
    • (1995) Diabetologia , vol.38 , pp. 1004-1005
    • Odawara, M.1    Tada, K.2    Yamashita, K.3
  • 15
    • 0027447027 scopus 로고
    • Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: Molecular genetic analysis and family study
    • Onishi H, Inoue K, Osaka H, Kimura S, Nagatomo H, Hanihara T, et al (1993): Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: Molecular genetic analysis and family study. J Neurol Sci 114:205-208.
    • (1993) J Neurol Sci , vol.114 , pp. 205-208
    • Onishi, H.1    Inoue, K.2    Osaka, H.3    Kimura, S.4    Nagatomo, H.5    Hanihara, T.6
  • 16
    • 0027337925 scopus 로고
    • 99mTc-HMPAO single photon emission tomography in late life depression: A pilot study of regional cerebral blood flow at rest and during a verbal fluency task
    • Philpot MP, Banerjee S, Needman-Bennett H, Costa DC (1993): 99mTc-HMPAO single photon emission tomography in late life depression: A pilot study of regional cerebral blood flow at rest and during a verbal fluency task. J Affect Disord 28:233-240.
    • (1993) J Affect Disord , vol.28 , pp. 233-240
    • Philpot, M.P.1    Banerjee, S.2    Needman-Bennett, H.3    Costa, D.C.4
  • 18
    • 0026637067 scopus 로고
    • Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthamoplegia
    • Soumalainen A, Majander A, Haltia M, Somer H, Lonnqvist J, Savontaus M-J, et al (1992): Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthamoplegia. J Clin Invest 90:61-66.
    • (1992) J Clin Invest , vol.90 , pp. 61-66
    • Soumalainen, A.1    Majander, A.2    Haltia, M.3    Somer, H.4    Lonnqvist, J.5    Savontaus, M.-J.6
  • 19
    • 0002470597 scopus 로고
    • Psychotic disturbance in mitochondrial diabetes due to 3243 mitochondrial tRNA mutation
    • Suzuki Y, Miyaoka H, Taniyama M, Atsumi Y, Hosokawa K, Tanaka Y, et al (1995): Psychotic disturbance in mitochondrial diabetes due to 3243 mitochondrial tRNA mutation. J Jpn Diab Soc 38:905-908.
    • (1995) J Jpn Diab Soc , vol.38 , pp. 905-908
    • Suzuki, Y.1    Miyaoka, H.2    Taniyama, M.3    Atsumi, Y.4    Hosokawa, K.5    Tanaka, Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.