Genotype‐phenotype analysis of MT‐ATP6‐associated Leigh syndrome von Na, Ji‐Hoon, Lee, Young‐Mock

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Heteroplasmic Mutant Load Differences in Mitochondrial DNA-Associated Leigh Syndrome von Na, Ji-Hoon, Lee, Young-Mock

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Diagnosis and Management of Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome von Na, Ji-Hoon, Lee, Young-Mock

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Mitochondrial tRNAHis mutation (m.12158A > G) associated with MELAS syndrome von Lee, Hyunjoo, Na, Ji‐Hoon, Lee, Young‐Mock

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Use of heteroplasmy rates for determining MELAS phenotype: a reply von Chae, Hyun-Wook, Lee, Young-Mock

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Therapeutic outcome of patients with Lennox-Gastaut syndrome with mitochondrial respiratory chain complex I deficiency von Na, Ji-Hoon, Lee, Young-Mock

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DYNC2H1 variants cause Leber congenital amaurosis without syndromic features von Lee, Junwon, Lee, Hyunjoo, Lee, Young‐Mock, Kuht, Helen J., Thomas, Mervyn G., Kim, Sang Jin, Lee, Seung‐Tae, Han, Jinu

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Focal cerebellar infarction as an initial sign of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes von Ko, Ara, Lee, Sang‐Jun, Lee, Young‐Mock

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Mitochondrial diabetes and mitochondrial DNA mutation load in MELAS syndrome von Chae, Hyun-Wook, Na, Ji-Hoon, Kim, Ho-Seong, Lee, Young-Mock

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Long-term Outcome of Resective Epilepsy Surgery in Patients With Lennox-Gastaut Syndrome von Kang, Joon Won, Eom, Soyong, Hong, William, Kwon, Hye Eun, Park, Soyoung, Ko, Ara, Kang, Hoon-Chul, Lee, Joon Soo, Lee, Young-Mock, Kim, Dong Seok, Kim, Heung Dong

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Enteral Tube Feeding in Paediatric Mitochondrial Diseases von Choi, Han Som, Lee, Young-Mock

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Preliminary Study of Neurodevelopmental Outcomes and Parenting Stress in Pediatric Mitochondrial Disease von Eom, Soyong, PhD, Lee, Young-Mock, MD, PhD

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Effective application of corpus callosotomy in pediatric intractable epilepsy patients with mitochondrial dysfunction von Na, Ji-Hoon, Kim, Heung Dong, Lee, Young-Mock

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Nusinersen for spinal muscular atrophy types II and III: a retrospective single-center study in South Korea von Shin, Hui Jin, Na, Ji-Hoon, Lee, Hyunjoo, Lee, Young-Mock

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Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations von Lee, Sunho, Na, Ji-Hoon, Lee, Young-Mock

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Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction von Na, Ji-Hoon, Kim, Heung-Dong, Lee, Young-Mock

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Avascular necrosis after long-term glucocorticoid treatment in MELAS: a cautionary note von Choi, Han Som, Lee, Jae Hyun, Lee, Sun Ho, Lee, Young-Mock

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Cause of Death in Children With Mitochondrial Diseases von Eom, Soyong, MD, PhD, Lee, Ha Neul, MD, Lee, Sunho, MD, Kang, Hoon-Chul, MD, PhD, Lee, Joon Soo, MD, PhD, Kim, Heung Dong, MD, PhD, Lee, Young-Mock, MD, PhD

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Nusinersen demonstrates effectiveness in treating spinal muscular atrophy: findings from a three-year nationwide study in Korea von Cho, Jaeso, Lee, Jiwon, Kim, Jihye, Lee, Hyunjoo, Kim, Min-Jee, Lee, Yun Jeong, Yum, Mi-Sun, Byun, Ji-Hye, Lee, Chong Guk, Lee, Young-Mock, Lee, Jeehun, Chae, Jong-Hee

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Central precocious puberty may be a manifestation of endocrine dysfunction in pediatric patients with mitochondrial disease von Chae, Hyun-Wook, Na, Ji-Hoon, Kwon, Ahreum, Kim, Ho-Seong, Lee, Young-Mock

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