712 Copyright © 2013 The Korean Society of Cardiology Korean Circulation Journal
Erratum
http://dx.doi.org/10.4070/kcj.2013.43.10.712 Print ISSN 1738-5520 • On-line ISSN 1738-5555
전체 글
http://dx.doi.org/10.4070/kcj.2013.43.10.712 Print ISSN 1738-5520 • On-line ISSN 1738-5555
관련 문서
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a common mitochondrial disease that can cause a wide range of clinical
caused by the point mutations of mtDNA are mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS, MIM# 540000), and myclonus epilepsy
A Case of Acute Tubulointerstitial Nephritis Associated with Rifampin Therapy Presenting as Fanconi-like Syndrome.. Jun Tae Park, Sik Lee, Won Kim, Sung Kwang Park, and Kyung
Pavlakis SG, Philips PC, Dimauro S, De vivo DC, Rowland LP: Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a distinctive
A Case of Lactate Containing Peritoneal Dialysis Solution Induced Lactic Acidosis Corrected by Changing
Diffusion and perfusion characteristics of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode) in thirteen patients.. The correct spelling
1 concerning the usefulness of muscle biopsy findings for diagnostic workup in patients with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes
We experienced a case of lactic acidosis in a 39-year-old man who visited an emergency room because of dyspnea, and the cause of lactic acidosis turned out to be recurrent