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  1. Loh TG
    Med J Malaya, 1972 Jun;26(4):256-61.
    PMID: 4220384
    Matched MeSH terms: Neuromuscular Diseases/diagnosis*
  2. Ahmad SS, Ghani SA
    Oman J Ophthalmol, 2012 May;5(2):115-7.
    PMID: 22993469
    Kearns-Sayre syndrome (KSS) belongs to the group of neuromuscular disorders known as mitochondrial encephalomyopathies. It has characteristic syndromal features, which include: chronic progressive external ophthalmoplegia, bilateral atypical pigmentary retinopathy, and cardiac conduction abnormalities. So far, only a single case has been reported where a patient with KSS had a normal retina. Herein, we report this extremely rare variant of KSS, which not only presented later than the normal age of presentation, but also had minimal pigmentary retinopathy.
    Matched MeSH terms: Neuromuscular Diseases
  3. Tay CH, Jek WT
    Med J Malaya, 1972 Jun;26(4):272-7.
    PMID: 5069417
    Matched MeSH terms: Neuromuscular Diseases*
  4. Mohamad F, Parent S, Pawelek J, Marks M, Bastrom T, Faro F, et al.
    J Pediatr Orthop, 2007 Jun;27(4):392-7.
    PMID: 17513958
    To evaluate the perioperative complications associated with surgical correction in neuromuscular scoliosis and to identify the risk factors associated with these complications.
    Matched MeSH terms: Neuromuscular Diseases/complications*
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