- A Case of MELAS Syndrome
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Kim KJ, Hwang YS, Choi YI, Park SH, Chi JG
- KMID: 1683654
- J Korean Pediatr Soc.
- 1990 Nov;33(11):1586-1592.
No abstract available. -
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- Acute Intestinal Pseudo-Obstruction in a Patient with MELAS Syndrome
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Choi PK, Kang HG
- KMID: 2405991
- J Korean Neurol Assoc.
- 2017 Nov;35(4):251-253.
- doi: 10.17340/jkna.2017.4.16
No abstract available. -
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- Total intravenous anesthesia with propofol and remifentanil in a patient with MELAS syndrome: A case report
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Park JS, Baek CW, Kang H, Cha SM, Park JW, Jung YH, Woo YC
- KMID: 2299343
- Korean J Anesthesiol.
- 2010 Apr;58(4):409-412.
- doi: 10.4097/kjae.2010.58.4.409
A 23-year-old woman with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) underwent a laparoscopy-assisted appendectomy. MELAS syndrome is a multisystemic disease caused by mitochondrial dysfunction. General anesthesia has... -
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- A Case of Early Onset MELAS Patient with Wolff-Parkinson-White Syndrome
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Kim JA, Ahn JM, Lee YM, Kang HC, Lee JS, Kim HD
- KMID: 2329491
- J Korean Child Neurol Soc.
- 2011 Dec;19(3):266-271.
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is one of the classic mitochondrial diseases characterized by symptoms of repeated episodes of hemiparesis with mitochondrial DNA mutation. We report... -
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- General Anesthesia with Sevoflurane for a Patient with MELAS (Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, Stroke-like Episodes) Syndrome: A case report
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Yoon SZ, Chung SH, Kim HS, Oh AY, Kim SD, Kim CS
- KMID: 2299149
- Korean J Anesthesiol.
- 2005 Sep;49(3):429-432.
- doi: 10.4097/kjae.2005.49.3.429
We describe the anesthetic management of a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, stroke-like episodes (MELAS) syndrome, and a form of mitochondrial myopathy. A 14 year-old-male with MELAS syndrome... -
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- Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS
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Finsterer
- KMID: 2450197
- Yonsei Med J.
- 2019 Apr;60(4):399-400.
- doi: 10.3349/ymj.2019.60.4.399
No abstract available. -
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- MELAS Syndrome Confirmed by Mitochondrial DNA Analysis in Siblings
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Rah YG, Chae SA, Lim IS, Lee DK, Yoo BH, Ko TS, Yoo HW
- KMID: 1946343
- J Korean Pediatr Soc.
- 1999 Mar;42(3):412-418.
MELAS(mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) syndrome is a major subgroup of mitochondrial myopathy. Recent advances in molecular genetics revealed specific mutations in mitochondrial DNA which cause MELAS.... -
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- A Case of Myopathy, Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MEALS) Syndrome with Intracardiac Thrombus
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Joo JC, Seol MD, Yoon JW, Lee YS, Kim DK, Choi YH, Ahn HS, Cho WH
- KMID: 2224968
- Korean Circ J.
- 2013 Mar;43(3):204-206.
- doi: 10.4070/kcj.2013.43.3.204
Myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) is a multisystem clinical syndrome manifested by mitochondrial myopathy, encephalopathy, lactic acidosis and recurrent stroke-like episodes. A 27-year-old female with MELAS syndrome... -
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- A Case of MELAS with Maternally Transmitted Type II Diabetes Mellitus and Deafness
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Yu HJ, Roh SY, Lee KE, Koh SH
- KMID: 2343269
- J Korean Neurol Assoc.
- 2007 Aug;25(3):416-418.
MELAS syndrome is typically a multisystemic disorder. We report one case of MELAS showing both maternally transmitted type II diabetes mellitus (DM) and deafness. A 41-year-old woman was admitted because... -
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- A Case of MELAS Syndrome Manifested by Insulin-deficient Diabetes Mellitus
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Jeong HS, Kang JY, Kim H, Lee KH, Lee DS, Choi GY, Oh TG, Jeon HJ
- KMID: 1965999
- J Korean Endocr Soc.
- 2008 Dec;23(6):444-449.
- doi: 10.3803/jkes.2008.23.6.444
MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes) syndrome is characterized by stroke-like episodes before the age of 40, encephalopathy, seizures, dementia and lactic acidosis, and is caused by mutations... -
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- Wolff-Parkinson-White Syndrome in a Patient With Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes Syndrome
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Lee MH, Sung YJ, Yoon JH, Kim J, Oh IY, Choi EK, Oh S
- KMID: 2225077
- Korean Circ J.
- 2011 Nov;41(11):674-676.
- doi: 10.4070/kcj.2011.41.11.674
Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome is a multisystem disorder, which is clinically characterized by encephalopathy, dementia, seizures and stroke-like episodes. Multiple organs can be affected and... -
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- Atypical Radiologic Manifestation of NARP Mimicking MELAS: a Case Report
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Lee Y, Lee D, Hwang H
- KMID: 2415891
- Investig Magn Reson Imaging.
- 2018 Jun;22(2):119-122.
- doi: 10.13104/imri.2018.22.2.119
Neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome is a rare maternally inherited mitochondrial disorder. Radiologic findings in NARP syndrome are varied; they include cerebral and cerebellar atrophy, basal ganglia... -
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- Alternating Hemispheric Seizures with Migrating Brain Lesions in MELAS Syndrome
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Moon SY, Hong SB, Song YM, Ryoo JW, Seo DW
- KMID: 2333387
- J Korean Epilepsy Soc.
- 2002 Jun;6(1):73-76.
Epileptic seizure is a frequent sign of mitochondrial encephalopathies with lactic acidosis and stroke-like episodes (MELAS). We report a 21-year-old woman with MELAS who had alternating hemispheric seizures. Her brain... -
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- A Case of MELAS Syndrome Presenting with Type 1 Diabetes Mellitus
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Jung CH, Roh E, Ahn CH, Kim LK, Lim S, Jang HC, Choi SH
- KMID: 2269086
- Korean J Med.
- 2015 Jun;88(6):706-710.
- doi: 10.3904/kjm.2015.88.6.706
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome presents with various clinical features, including seizures, stroke-like episodes, encephalopathy, myopathy, cardiac involvement, and diabetes. However, due to its clinical heterogeneity,... -
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- A Case Report of MELAS Syndrome
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Lee TY, Hong DK, Lim SR, Heo K, Cho HK
- KMID: 2138123
- J Korean Neurol Assoc.
- 1993 Jun;11(2):254-260.
Mitochondnal encephalomyopathies are multisysternic diseases affecting predominantly the CNS and skeletal muscLes by mitochondrial dysfunction. Mitochondrial diseases include three distinct syndromes: mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS):... -
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- A Case of Pure Word Deafness in MELAS Syndrome
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Shin DS, Kwon OS, Lee HO, Youn YC
- KMID: 2137946
- J Korean Neurol Assoc.
- 2004 Oct;22(5):520-523.
An 18-year-woman was referred with seizure activity and global aphasia. Diagnosis of MELAS syndrome with left temporo-parieto-occipital infarction was confirmed by gene analysis. Global aphasia was improved completely. Right temporal... -
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- A Two Cases of MELAS in Siblings
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Yeon YY, Choi BJ, Kim YH, Kim JW, Park SS, Ji JG, Whang KT
- KMID: 2329217
- J Korean Child Neurol Soc.
- 1997 Oct;5(1):138-146.
MELAS is the condition associated with mutant mtDNA that most closely mimics thrombotic cerebrovascular disease. It is characterized by mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes. These children develop short... -
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- MELAS syndrome in a child: CT and MR findings
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Choi HY, Hong SJ, Cho JH, Suh DC, Hong CY
- KMID: 2348879
- J Korean Radiol Soc.
- 1993 Feb;29(1):160-164.
MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) is one of the mitochondrial encephalomyopathy, A rare disease caused by a disturbance of the mitochondrial chain of respiration. MELAS is confirmed... -
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- Dexmedetomidine as a non-triggering anesthetic agent in a patient with MELAS syndrome and systemic sepsis: A case report
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Kim SH, Park SY, Jung KT
- KMID: 2465339
- Anesth Pain Med.
- 2019 Oct;14(4):416-422.
- doi: 10.17085/apm.2019.14.4.416
BACKGROUND: The selection of anesthetic agents is important in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome patient because serious and unexpected complications can occur after anesthetic exposure. CASE:... -
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- The Author Reply: Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS
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Lee YM
- KMID: 2450198
- Yonsei Med J.
- 2019 Apr;60(4):401-401.
- doi: 10.3349/ymj.2019.60.4.401
No abstract available. -
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