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Volumn 118, Issue 2, 2008, Pages 267-275

Delayed diagnosis of Kearns-Sayre syndrome in a 38-year-old male patient: A case report

Author keywords

And histopathologic findings; Clinical; Kearns Sayre syndrome; Laboratory

Indexed keywords

CARBAMAZEPINE;

EID: 38349134612     PISSN: 00207454     EISSN: 15635279     Source Type: Journal    
DOI: 10.1080/00207450701242669     Document Type: Article
Times cited : (1)

References (20)
  • 1
    • 0028918471 scopus 로고
    • Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects
    • Anan, R., Nakagawa, M., Miyata, M., Higuchi, I., Nakao, S., Suehara, M., Osame, M., & Tanaka, H. (1995). Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects. Circulation, 91(4), 955-61.
    • (1995) Circulation , vol.91 , Issue.4 , pp. 955-961
    • Anan, R.1    Nakagawa, M.2    Miyata, M.3    Higuchi, I.4    Nakao, S.5    Suehara, M.6    Osame, M.7    Tanaka, H.8
  • 3
    • 0031595077 scopus 로고    scopus 로고
    • Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease
    • Boles, R. G., Roe, T., Senadheera, D., Mahnovski, V., & Wong, L. J. (1998). Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease. European Journal of Pediatrics, 157(8), 643-647.
    • (1998) European Journal of Pediatrics , vol.157 , Issue.8 , pp. 643-647
    • Boles, R.G.1    Roe, T.2    Senadheera, D.3    Mahnovski, V.4    Wong, L.J.5
  • 4
    • 0033761979 scopus 로고    scopus 로고
    • Mitochondrial DNA mutations in the pathogenesis of human disease
    • Chinnery, P. F., & Turnbull, D. M. (2000). Mitochondrial DNA mutations in the pathogenesis of human disease. Molecular Medicine Today, 6(11), 425-432.
    • (2000) Molecular Medicine Today , vol.6 , Issue.11 , pp. 425-432
    • Chinnery, P.F.1    Turnbull, D.M.2
  • 8
    • 0026773036 scopus 로고
    • Endocrine dysfunction in Kearns-Sayre syndrome
    • Harvey, J. N., & Barnett, D. (1992). Endocrine dysfunction in Kearns-Sayre syndrome. Clinical Endocrinology (Oxf.), 37(1), 97-103.
    • (1992) Clinical Endocrinology (Oxf.) , vol.37 , Issue.1 , pp. 97-103
    • Harvey, J.N.1    Barnett, D.2
  • 11
    • 4043063576 scopus 로고    scopus 로고
    • Kearns-Sayre syndrome. A case with literature review
    • Koc, F., Zorludemir, S., & Sarica, Y. (2003). Kearns-Sayre syndrome. A case with literature review. Marmara Medical Journal, 16, 116-120.
    • (2003) Marmara Medical Journal , vol.16 , pp. 116-120
    • Koc, F.1    Zorludemir, S.2    Sarica, Y.3
  • 12
    • 0029127326 scopus 로고
    • Evidence for cardioembolic stroke in a case of Kearns-Sayre syndrome
    • Kosinski, C., Mull, M., Lethen, H., & Topper, R. (1995). Evidence for cardioembolic stroke in a case of Kearns-Sayre syndrome. Stroke, 26(10), 1950-1952.
    • (1995) Stroke , vol.26 , Issue.10 , pp. 1950-1952
    • Kosinski, C.1    Mull, M.2    Lethen, H.3    Topper, R.4
  • 13
    • 0016811173 scopus 로고
    • Chronic progressive external ophthalmoplegia, pigmentary retinopathy, and heart block (Kearns-Sayre syndrome). Report of a case
    • Lowes, M. (1975). Chronic progressive external ophthalmoplegia, pigmentary retinopathy, and heart block (Kearns-Sayre syndrome). Report of a case. Acta Ophthalmologica (Copenh), 53(4), 610-619.
    • (1975) Acta Ophthalmologica (Copenh) , vol.53 , Issue.4 , pp. 610-619
    • Lowes, M.1
  • 15
    • 0029040769 scopus 로고
    • Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome
    • Poulton, J., O'Rahilly, S., Morten, K. J., & Clark, A. (1995). Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome. Diabetologia, 38(7), 868-871.
    • (1995) Diabetologia , vol.38 , Issue.7 , pp. 868-871
    • Poulton, J.1    O'Rahilly, S.2    Morten, K.J.3    Clark, A.4
  • 18
    • 0018420761 scopus 로고
    • Familial Kearns-Sayre syndrome
    • Schnitzler, E. R., & Robertson, W. C., Jr.. (1979). Familial Kearns-Sayre syndrome. Neurology, 29(8), 1172-1174.
    • (1979) Neurology , vol.29 , Issue.8 , pp. 1172-1174
    • Schnitzler, E.R.1    Robertson Jr., W.C.2
  • 19
    • 0343632387 scopus 로고    scopus 로고
    • Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: A clinical and molecular genetic study of four children with Kearns-Sayre syndrome
    • Wilichowski, E., Gruters, A., Kruse, K., Rating, D., Beetz, R., Korenke, G. C., Ernst, B. P., Christen, H. J., & Hanefeld, F. (1997). Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: A clinical and molecular genetic study of four children with Kearns-Sayre syndrome. Pediatric Research, 41(2), 193-200.
    • (1997) Pediatric Research , vol.41 , Issue.2 , pp. 193-200
    • Wilichowski, E.1    Gruters, A.2    Kruse, K.3    Rating, D.4    Beetz, R.5    Korenke, G.C.6    Ernst, B.P.7    Christen, H.J.8    Hanefeld, F.9
  • 20
    • 0031732194 scopus 로고    scopus 로고
    • Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy
    • Zanssen, S., Molnar, M., Buse, G., & Schroder, J. M. (1998). Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy. Clinical Neuropathology, 17(6), 291-296.
    • (1998) Clinical Neuropathology , vol.17 , Issue.6 , pp. 291-296
    • Zanssen, S.1    Molnar, M.2    Buse, G.3    Schroder, J.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.