Literature DB >> 1033489

Erythrocyte shape in Duchenne muscular dystrophy.

D W Matheson, W K Engel, E C Derrer.   

Abstract

In a controlled and blind study we were not able to identify any abnormality of erythrocytes of eight patients with Duchenne muscular dystrophy compared with seven approximately age-matched unaffected siblings (six males, one female step-sibling). Erythrocyte morphology was found to be very sensitive to various types of cell treatment. At this time, erythrocyte morphology, evaluated by the techniques used, should not be considered an established diagnostic test for the Duchenne muscular dystrophy patient or carrier.

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Year:  1976        PMID: 1033489     DOI: 10.1212/wnl.26.12.1182

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

1.  Erythrocyte ghost (Na+ + K+) ATPase activity in mice with hereditary muscular dystrophy (strain C57 BL/64J/dy).

Authors:  G Souweine; M O Rolland; I Maire; M C Donas
Journal:  J Neurol       Date:  1978-02-14       Impact factor: 4.849

2.  Scanning electron microscopy studies of erythrocytes in spinocerebellar degeneration.

Authors:  Y Yasuda; I Akiguchi; H Shio; M Kameyama
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-03       Impact factor: 10.154

3.  Osmotic fragility of erythrocytes in myopathies.

Authors:  A D Korczyn; E Nadler; G Falewski de Leon
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

  3 in total

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