Literature DB >> 26156707

Exertional rhabdomyolysis, profound lactic acidosis, and acute kidney injury in a young boy: Answers.

Min-Hua Tseng1,2, Shao-Hsuan Hsia3, Ching-Shiang Chi4, Ju-Li Lin5, Jainn-Jim Lin3, Shih-Hua Lin6,7.   

Abstract

Entities:  

Keywords:  Lactic acidosis; Mitochondrial myopathy; Rhabdomyolysis

Mesh：

Year:  2015        PMID： 26156707     DOI： 10.1007/s00467-015-3150-2

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


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  4 in total

1.  A pathogenesis-associated mutation in human mitochondrial tRNALeu(UUR) leads to reduced 3'-end processing and CCA addition.

Authors:  Louis Levinger; Isabel Oestreich; Catherine Florentz; Mario Mörl
Journal:  J Mol Biol       Date:  2004-03-26       Impact factor: 5.469

Review 2.  Metabolic myopathies: a clinical approach; part I.

Authors:  B T Darras; N R Friedman
Journal:  Pediatr Neurol       Date:  2000-02       Impact factor: 3.372

3.  Oral glucose lactate stimulation test in mitochondrial disease.

Authors:  C S Chi; S C Mak; W J Shian; C H Chen
Journal:  Pediatr Neurol       Date:  1992 Nov-Dec       Impact factor: 3.372

4.  MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

Authors:  A Chomyn; A Martinuzzi; M Yoneda; A Daga; O Hurko; D Johns; S T Lai; I Nonaka; C Angelini; G Attardi
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-15       Impact factor: 11.205
  4 in total

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