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Volumn 50, Issue 1, 1998, Pages 299-300

Rhabdomyolysis in autosomal dominant progressive external ophthalmoplegia

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; MITOCHONDRIAL DNA; MYOGLOBIN;

EID: 0031929664     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.50.1.299     Document Type: Article
Times cited : (27)

References (10)
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    • (1994) Myology, Vol 2. 2nd Ed. , vol.2 , pp. 1679-1696
    • Penn, A.S.1
  • 2
    • 0000902925 scopus 로고
    • Myopathies due to drugs, toxins, and nutritional deficiency
    • Engel AG, Franzini-Armstrong C, eds. 2nd ed. New York: McGraw-Hill
    • Victor M, Sieb JP. Myopathies due to drugs, toxins, and nutritional deficiency. In: Engel AG, Franzini-Armstrong C, eds. Myology, vol. 2. 2nd ed. New York: McGraw-Hill, 1994:1697-1725.
    • (1994) Myology , vol.2 , pp. 1697-1725
    • Victor, M.1    Sieb, J.P.2
  • 3
    • 0029978895 scopus 로고    scopus 로고
    • Muscle-nerve involvement in autosomal dominant progressive external ophthalmoplegia with hypogonadism
    • Melberg A, Lundberg PO, Henriksson KG, Olsson Y, Stålberg E. Muscle-nerve involvement in autosomal dominant progressive external ophthalmoplegia with hypogonadism. Muscle Nerve 1996;19:751-757.
    • (1996) Muscle Nerve , vol.19 , pp. 751-757
    • Melberg, A.1    Lundberg, P.O.2    Henriksson, K.G.3    Olsson, Y.4    Stålberg, E.5
  • 4
    • 0029821848 scopus 로고    scopus 로고
    • Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism
    • Melberg A, Arnell H, Dahl N, et al. Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism. Muscle Nerve 1996;19:1561-1569.
    • (1996) Muscle Nerve , vol.19 , pp. 1561-1569
    • Melberg, A.1    Arnell, H.2    Dahl, N.3
  • 5
    • 0029834809 scopus 로고    scopus 로고
    • Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia
    • Moslemi A-R, Melberg A, Holme E, Oldfors A. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia. Ann Neurol 1996;40:707-713.
    • (1996) Ann Neurol , vol.40 , pp. 707-713
    • Moslemi, A.-R.1    Melberg, A.2    Holme, E.3    Oldfors, A.4
  • 6
    • 0025828342 scopus 로고
    • Mitochondrial DNA deletions in inherited recurrent myoglobinuria
    • Ohno K, Tanaka M, Sahashi K, et al. Mitochondrial DNA deletions in inherited recurrent myoglobinuria. Ann Neurol 1991;29:364-369.
    • (1991) Ann Neurol , vol.29 , pp. 364-369
    • Ohno, K.1    Tanaka, M.2    Sahashi, K.3
  • 7
    • 0028229765 scopus 로고
    • Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy
    • Checcarelli N, Prelle A, Moggio M, et al. Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy. J Neurol Sci 1994;123:74-79.
    • (1994) J Neurol Sci , vol.123 , pp. 74-79
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  • 8
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    • Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy
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    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 2379-2382
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  • 9
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    • A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria
    • Keightley JA, Hoffbuhr KC, Burton MD, et al. A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria. Nat Genet 1996; 12:410-416.
    • (1996) Nat Genet , vol.12 , pp. 410-416
    • Keightley, J.A.1    Hoffbuhr, K.C.2    Burton, M.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.