Literature DB >> 29559858

Letter to the Editor: Diagnosing Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes (MELAS) Requires Not Only Phenotypic But Also Genotypic Verification.

Josef Finsterer1, Sinda Zarrouk-Mahjoub2.   

Abstract

Entities:  

Year:  2018        PMID： 29559858      PMCID： PMC5855420     

Source DB:  PubMed          Journal:  Ochsner J        ISSN： 1524-5012


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  3 in total

1.  Mitochondrial A3243G mutation with manifestation of acute dilated cardiomyopathy.

Authors:  Nicolas Stalder; Nuray Yarol; Piergiorgio Tozzi; Samuel Rotman; Michael Morris; Florence Fellmann; Juerg Schwitter; Roger Hullin
Journal:  Circ Heart Fail       Date:  2012-01       Impact factor: 8.790

Review 2.  Molecular pathology of MELAS and L-arginine effects.

Authors:  Yasutoshi Koga; Nataliya Povalko; Junko Nishioka; Koujyu Katayama; Shuichi Yatsuga; Toyojiro Matsuishi
Journal:  Biochim Biophys Acta       Date:  2011-09-14

3.  Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes-MELAS Syndrome.

Authors:  Caitlin Henry; Neema Patel; William Shaffer; Lillian Murphy; Joe Park; Bradley Spieler
Journal:  Ochsner J       Date:  2017
  3 in total

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