Literature DB >> 4374513

Oculopharyngeal muscular dystrophy. A case with abnormal mitochondria and "fingerprint" inclusions.

J Julien, C Vital, J M Vallat, M Vallat, M Le Blanc.   

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Year:  1974        PMID: 4374513     DOI: 10.1016/0022-510x(74)90067-7

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


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  7 in total

1.  Fingerprint inclusions and circular structures in the muscle. Report of a case.

Authors:  S Matsubara; W G Mair
Journal:  Acta Neuropathol       Date:  1979-07-13       Impact factor: 17.088

2.  Oculopharyngeal myopathy with distal and cardiomyopathy.

Authors:  I Goto; Y Kanazawa; T Kobayashi; Y Murai; Y Kuroiwa
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-06       Impact factor: 10.154

3.  Nuclear inclusions in oculopharyngeal dystrophy.

Authors:  F M Tomé; M Fardeau
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

4.  Oculopharyngeal dystrophy diagnostic problems and possibilities.

Authors:  L A Bastiaensen; B P Schulte
Journal:  Doc Ophthalmol       Date:  1979-03-15       Impact factor: 2.379

5.  Fingerprint inclusions in normal fetal muscle.

Authors:  M W Ambler; C Neave; R Entwistle
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

6.  [Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)].

Authors:  G Spalke; R Heene; D Herold
Journal:  J Neurol       Date:  1975       Impact factor: 4.849

7.  Oculopharyngeal dystrophy: ultrastructure of muscles distinct from the primary myopathy.

Authors:  J W Kozachek; F J Wilson
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

  7 in total

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