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지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 저널정보
- 대한치매학회 Dementia and Neurocognitive Disorders(대한치매학회지) Dementia and Neurocognitive Disorders(대한치매학회지) 제9권 제2호
- 발행연도
- 2010.1
- 수록면
- 69 - 73 (5page)
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초록· 키워드
오류제보하기
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)uncommonly develops after the age of 40. We describe a patient with MELAS whose first strokelike episode presented at age 65, followed by two more episodes. The brain MR imaging for each stroke-like episode demonstrated hyperintense lesion in diffusion weighted image (DWI),and variable signal intensities in apparent diffusion coefficient (ADC) maps in temporo-parietal and occipital regions. We diagnosed the patient as MELAS with 3243A>G point mutation.
목차
등록된 정보가 없습니다.
참고문헌 (23)
참고문헌 신청
Bosbach S / 2003 / Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and kearns-sayre syndrome / Brain 126 : 1231 ~ 1240
Dickerson BC / 2005 / Case records of the massachusetts general hospital. Case 36-2005. A 61-year-old woman with seizure, disturbed gait, and altered mental status / N Engl J
Goto Y / 1990 / A mutation in the trna(leu)(uur) gene associated with the melas subgroup of mitochondrial encephalomyopathies / Nature 348 : 651 ~ 653
Goto Y / 1992 / Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (melas): a correlative study of the clinical features and mitochondrial DNA
Hirano M / 1992 / Melas: an original case and clinical criteria for diagnodiagnosis / Neuromuscul Disord 2 : 125 ~ 135
Dickerson BC / 2005 / Case records of the massachusetts general hospital. Case 36-2005. A 61-year-old woman with seizure, disturbed gait, and altered mental status / N Engl J
Goto Y / 1990 / A mutation in the trna(leu)(uur) gene associated with the melas subgroup of mitochondrial encephalomyopathies / Nature 348 : 651 ~ 653
Goto Y / 1992 / Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (melas): a correlative study of the clinical features and mitochondrial DNA
Hirano M / 1992 / Melas: an original case and clinical criteria for diagnodiagnosis / Neuromuscul Disord 2 : 125 ~ 135
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50대에 진단된 MELAS 증후군 1예
대한내과학회지
2011 .01
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가역적인 뇌기능장애를 보인 MELAS 증후군
Annals of Clinical Neurophysiology
2006 .01
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제1형 당뇨병이 발생하여 진단된 MELAS 증후군 1예
대한내과학회지
2015 .01
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The Usefulness of Muscle Biopsy in Initial Diagnostic Evaluation of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes
Yonsei Medical Journal
2019 .01
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Mutation analyses in Korean patients with MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes)
Journal of genetic medicine
1997 .01
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한방치료 후 호전된 MELAS 증후군 증례 1례
대한한의학방제학회지
2010 .01
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Twenty-one-year follow-up of variable onset MELAS syndrome with heteroplasmic nt3243A>G mtDNA mutation: A case report
Journal of genetic medicine
2019 .01
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다양한 임상경과를 보인 멜라스(MELAS, mitochondrial encephalopathy, lactic acidosis, and stroke-like episode) 증후군 2례
대한유전성대사질환학회지
2016 .01
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동기능 부전을 동반한 MELAS 증후군 1예
대한내과학회지
2013 .01
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Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS
Yonsei Medical Journal
2019 .01
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Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episode Syndrome Presenting with Prolonged Visual Aura
Journal of Clinical Neurology
2015 .01
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Tc-99m ECD Brain SPECT in MELAS Syndrome and Mitochondrial Myopathy: Comparison with MR findings
대한핵의학회지
1998 .01
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