Literature DB >> 17692973

Adult-onset hypertrophic cardiomyopathy manifested as initial major presentation of mitochondrial disease with A-to-G 3243 tRNA (Leu(UUR)) point mutation.

Po-Chao Hsu, Chih-Sheng Chu, Tsung-Hsien Lin, Ye-Hsu Lu, Chee-Siong Lee, Wen-Ter Lai, Sheng-Hsiung Sheu.   

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Year:  2007        PMID： 17692973     DOI： 10.1016/j.ijcard.2007.06.098

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN： 0167-5273            Impact factor:   4.164


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  4 in total

Review 1.  Cardiological manifestations of mitochondrial respiratory chain disorders.

Authors:  A Berardo; O Musumeci; A Toscano
Journal:  Acta Myol       Date:  2011-06

2.  Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load.

Authors:  Kieren G Hollingsworth; Grainne S Gorman; Michael I Trenell; Robert McFarland; Robert W Taylor; Douglass M Turnbull; Guy A MacGowan; Andrew M Blamire; Patrick F Chinnery
Journal:  Neuromuscul Disord       Date:  2012-04-17       Impact factor: 4.296

3.  Multiple neurologic, psychiatric, and endocrine complaints in a young woman: a case discussion and review of the clinical features and management of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke.

Authors:  Chaya G Bhuvaneswar; Jared L Goetz; Theodore A Stern
Journal:  Prim Care Companion J Clin Psychiatry       Date:  2008

Review 4.  tRNA-Derived Small RNAs and Their Potential Roles in Cardiac Hypertrophy.

Authors:  Jun Cao; Douglas B Cowan; Da-Zhi Wang
Journal:  Front Pharmacol       Date:  2020-09-17       Impact factor: 5.810
  4 in total

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