- Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases
-
Choi BO, Hwang JH, Cho EM, Jeong EH, Hyun YS, Jeon HJ, Seong KM, Cho NS, Chung KW
- KMID: 1078360
- Exp Mol Med.
- 2010 Jun;42(6):446-455.
- doi: 10.3858/emm.2010.42.6.046
Mitochondrial diseases are clinically and genetically heterogeneous disorders, which make the exact diagnosis and classification difficult. The purpose of this study was to identify pathogenic mtDNA mutations in 61 Korean... -
- CITED
-
- Close
- SHARE
-
- Close
- Diffusion-weighted image and MR spectroscopic analysis of a case of MELAS with repeated attacks
-
Kim HS, Kim DI, Lee BI, Jeong EK, Choi C, Lee JD, Yoon PH, Kim EJ, Kim SH, Yoon YK
- KMID: 720596
- Yonsei Med J.
- 2001 Feb;42(1):128-133.
- doi: 10.3349/ymj.2001.42.1.128
We report the clinical and MR manifestations of an 18 year-old girl with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. Recurrent status epilepticus caused... -
- CITED
-
- Close
- SHARE
-
- Close
