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The Author Reply: Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions
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참고문헌 (6)
- Kisler JE, "Mitochondrial diseases in childhood : a clinical approach to investigation and management", Dev Med Child Neurol, 52, pp.422~433 (2010)
- Horvath R, "Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene", Brain, 129(Pt 7), pp.1674~1684 (2006)
- Finsterer J, "Leigh and Leigh-like syndrome in children and adults", Pediatr Neurol, 39, pp.223~235 (2008)
- 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]
- Eom S, "Cause of death in children with mitochondrial diseases", Pediatr Neurol, 66, pp.82~88 (2017)
- López-Gallardo E, "CPEO and KSS differ in the percentage and location of the mtDNA deletion", Mitochondrion, 9, pp.314~317 (2009)
관련 논문AI추천
Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA DeletionsJosef Finsterer연세대학교의과대학 · Yonsei Medical Journal2019 · 제60권 제2호The Author Reply: Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS이영목연세대학교의과대학 · Yonsei Medical Journal2019 · 제60권 제4호Clinical Features of Leber Hereditary Optic Neuropathy Carrying a Rare m.13051G>A Mitochondrial Mutation: A Case ReportHee Kyung Yang, Hyuna Kim, Jeong-Min Hwang, Moon-Woo Seong대한안과학회 · Korean Journal of Ophthalmology2025 · 제39권 제6호Re: Comments on “Stroke-Like Episode, Aphasia, and Hearing Loss in MELAS”Asael Lubotzky대한신경과학회 · Journal of Clinical Neurology2025 · 제21권 제5호Comments on: “Stroke-Like Episode, Aphasia, and Hearing Loss in MELAS”Josef Finsterer대한신경과학회 · Journal of Clinical Neurology2025 · 제21권 제5호Re: Comments on “A Case of MELAS With the m.3243A>G Variant of the MT-TL1 Gene Mimicking Acute Intermittent Porphyria”: The Authors RespondShilin Yang, Wenjie Cai, Xiang Han대한신경과학회 · Journal of Clinical Neurology2022 · 제18권 제5호
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