Literature DB >> 868828

Kearns-Sayre syndrome: the importance of early recognition.

A M Seigel, B A Shaywitz, T Ciesielski.   

Abstract

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Mesh：

Year:  1977        PMID： 868828     DOI： 10.1001/archpedi.1977.02120190105025

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  3 in total

1.  Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

Authors:  C Doriguzzi; L Palmucci; T Mongini; N Bresolin; L Bet; G Comi; R Lala
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-01       Impact factor: 10.154

2.  Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.

Authors:  J Egger; B D Lake; J Wilson
Journal:  Arch Dis Child       Date:  1981-10       Impact factor: 3.791

3.  Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).

Authors:  S Suzuki; Y Hinokio; S Hirai; M Onoda; M Matsumoto; M Ohtomo; H Kawasaki; Y Satoh; H Akai; K Abe
Journal:  Diabetologia       Date:  1994-08       Impact factor: 10.122
  3 in total

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