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Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS
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참고문헌 (5)
- 백민성, "The Usefulness of Muscle Biopsy in Initial Diagnostic Evaluation of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes", Yonsei Medical Journal, 60(1), pp.98~105 (2019), 연세대학교의과대학[DOI]
- "GeneReviews®" (1993)[URL]
- Poulton J, "Genetic counselling for maternally inherited mitochondrial disorders", Mol Diagn Ther, 21, pp.419~429 (2017)
- Mezuki S, "Isolated and repeated stroke-like episodes in a middleaged man with a mitochondrial ND3 T10158C mutation : a case report", BMC Neurol, 17, pp.217~ (2017)
- Finsterer J, "Toxicity of Antiepileptic Drugs to Mitochondria", Handb Exp Pharmacol, 240, pp.473~488 (2017)
관련 논문AI추천
The Author Reply: Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS이영목연세대학교의과대학 · Yonsei Medical Journal2019 · 제60권 제4호A Case of MELAS With the m.3243A>G Variant of the MT-TL1 Gene Mimicking Acute Intermittent PorphyriaShilin Yang, Wenjie Cai, Xiang Han대한신경과학회 · Journal of Clinical Neurology2022 · 제18권 제3호Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA DeletionsJosef Finsterer연세대학교의과대학 · Yonsei Medical Journal2019 · 제60권 제2호The Usefulness of Muscle Biopsy in Initial Diagnostic Evaluation of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes김세훈, 백민성, 이영목연세대학교의과대학 · Yonsei Medical Journal2019 · 제60권 제1호Stroke-Like Episode, Aphasia, and Hearing Loss in MELASAsael Lubotzky, Michael Teitcher대한신경과학회 · Journal of Clinical Neurology2025 · 제21권 제3호Comments on “A Case of MELAS With the m.3243A>G Variant of the MT-TL1 Gene Mimicking Acute Intermittent Porphyria”Josef Finsterer대한신경과학회 · Journal of Clinical Neurology2022 · 제18권 제5호
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