메뉴 건너뛰기




Volumn 10, Issue 1, 2000, Pages 56-58

Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction

Author keywords

Intestinal pseudo obstruction; Mitochondrial DNA; Mitochondrial encephalomyopathy; Single mitochondrial DNA deletion

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0033988268     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(99)00072-3     Document Type: Article
Times cited : (16)

References (8)
  • 1
    • 0002629236 scopus 로고    scopus 로고
    • Mitochondrial encephalomyopathies
    • R.N. Rosenberg, S.B. Prusiner, S. DiMauro, & R.L. Barch. Boston: Butterworth-Heinemann
    • DiMauro S., Bonilla E. Mitochondrial encephalomyopathies. Rosenberg R.N., Prusiner S.B., DiMauro S., Barch R.L., The molecular and genetic basis of neurological disease. 1997;201-235 Butterworth-Heinemann, Boston.
    • (1997) The Molecular and Genetic Basis of Neurological Disease , pp. 201-235
    • Dimauro, S.1    Bonilla, E.2
  • 2
    • 6844258202 scopus 로고    scopus 로고
    • Primary adrenal insufficiency in a child with a mitochondrial DNA deletion
    • Bruno C., Minetti C., Tang Y., et al. Primary adrenal insufficiency in a child with a mitochondrial DNA deletion. J Inher Metab Dis. 21:1998;155-161.
    • (1998) J Inher Metab Dis , vol.21 , pp. 155-161
    • Bruno, C.1    Minetti, C.2    Tang, Y.3
  • 4
    • 0031594759 scopus 로고    scopus 로고
    • Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid
    • Tengan C.H., Kiyomoto B.H., Rocha M.S., Tabares V.L., Gabbai A.A., Moraes C.T. Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid. J Clin Endocrinol Metab. 83:1998;125-129.
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 125-129
    • Tengan, C.H.1    Kiyomoto, B.H.2    Rocha, M.S.3    Tabares, V.L.4    Gabbai, A.A.5    Moraes, C.T.6
  • 5
    • 0026840463 scopus 로고
    • New morphological approaches to the study of mitochondrial encephalomyopathies
    • Bonilla E., Sciacco M., Tanji K., et al. New morphological approaches to the study of mitochondrial encephalomyopathies. Brain Pathol. 2:1992;113-119.
    • (1992) Brain Pathol , vol.2 , pp. 113-119
    • Bonilla, E.1    Sciacco, M.2    Tanji, K.3
  • 6
    • 0023429777 scopus 로고
    • Cytochrome c oxidase deficiency in Leigh syndrome
    • DiMauro S., Servidei S., Zeviani M., et al. Cytochrome c oxidase deficiency in Leigh syndrome. Ann Neurol. 22:1987;498-506.
    • (1987) Ann Neurol , vol.22 , pp. 498-506
    • Dimauro, S.1    Servidei, S.2    Zeviani, M.3
  • 7
    • 0029144941 scopus 로고
    • Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome
    • Campos Y., García-Silva T., Barrionuevo C.R., Cabello A., Muley R., Arenas J. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome. Pediatr Neurol. 13:1995;69-72.
    • (1995) Pediatr Neurol , vol.13 , pp. 69-72
    • Campos, Y.1    García-Silva, T.2    Barrionuevo, C.R.3    Cabello, A.4    Muley, R.5    Arenas, J.6
  • 8
    • 0028301915 scopus 로고
    • Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
    • Hirano M., Silvestri G., Blake D.M., et al. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder. Neurology. 44:1994;721-727.
    • (1994) Neurology , vol.44 , pp. 721-727
    • Hirano, M.1    Silvestri, G.2    Blake, D.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.