Literature DB >> 10658170

Mitochondrial myopathy diagnosis.

J M Shoffner1.   

Abstract

Oxidative phosphorylation (OXPHOS) accounts for approximately 95% of the adenosine triphosphate (ATP) produced by the cell. The central nervous system, peripheral nervous system, cardiac muscle, skeletal muscle, and smooth muscle are highly susceptible to dysfunction of this complex enzyme system. Although most OXPHOS diseases are multisystem disorders, the neuromuscular manifestations are often prominent and play an important role in patient diagnosis. To assist the neurologist in evaluating these complex patients, this article focuses on selected samples of OXPHOS diseases with identifiable neuromuscular abnormalities and presents an evaluation algorithm to facilitate patient diagnosis.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10658170     DOI: 10.1016/s0733-8619(05)70180-8

Source DB:  PubMed          Journal:  Neurol Clin        ISSN: 0733-8619            Impact factor:   3.806


  5 in total

1.  Differential expression of oxidative phosphorylation genes in patients with Alzheimer's disease: implications for early mitochondrial dysfunction and oxidative damage.

Authors:  Maria Manczak; Byung S Park; Youngsin Jung; P Hemachandra Reddy
Journal:  Neuromolecular Med       Date:  2004       Impact factor: 3.843

2.  An autopsy case of chronic progressive external ophthalmoplegia with renal insufficiency.

Authors:  Takashi Yuri; Yaeko Kondo; Keiko Kohno; Yen-Chang Lei; Seika Kanematsu; Maki Kuwata; Toshiji Iwasaka; Airo Tsubura
Journal:  Med Mol Morphol       Date:  2008-12-24       Impact factor: 2.309

Review 3.  Presentation and diagnosis of mitochondrial disorders in children.

Authors:  Mary Kay Koenig
Journal:  Pediatr Neurol       Date:  2008-05       Impact factor: 3.372

4.  Cerebrovascular complications in pediatric intensive care unit.

Authors:  Anil Sachdev; Rachna Sharma; Dhiren Gupta
Journal:  Indian J Crit Care Med       Date:  2010-07

5.  Hybrid gel electrophoresis using skin fibroblasts to aid in diagnosing mitochondrial disease.

Authors:  Christopher Newell; Aneal Khan; David Sinasac; John Shoffner; Marisa W Friederich; Johan L K Van Hove; Stacey Hume; Jane Shearer; Iveta Sosova
Journal:  Neurol Genet       Date:  2019-05-01
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.