Literature DB >> 902666

Familial progressive external ophthalmoplegia with abnormal muscle mitochondria.

E Jankowicz, H Berger, S Kurasz, W Winogrodzka, L Eljasz.   

Abstract

Entities:  

Mesh：

Year:  1977        PMID： 902666     DOI： 10.1159/000114820

Source DB:  PubMed          Journal:  Eur Neurol        ISSN： 0014-3022            Impact factor:   1.710


× No keyword cloud information.
  5 in total

Review 1.  Mitochondrial myopathy: a genetic study of 71 cases.

Authors:  A E Harding; R K Petty; J A Morgan-Hughes
Journal:  J Med Genet       Date:  1988-08       Impact factor: 6.318

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.  Ophthalmoplegia-plus.

Authors:  V Godel; P Nemet; I Reider-Groswasser; G Messer; M Lazar
Journal:  Doc Ophthalmol       Date:  1981-11       Impact factor: 2.379

4.  Kearns syndrome: a heterogeneous group of disorders with CPEO, or a nosological entity?

Authors:  L A Bastiaensen; C W Frenken; H J Ter Laak; H H Jaspar; A M Stadhouders; W Ruitenbeek; J H Veerkamp
Journal:  Doc Ophthalmol       Date:  1982-01-29       Impact factor: 2.379

5.  Ophthalmoplegia plus. A multisystem disorder of unknown etiopathogenesis.

Authors:  G Pellegrini; G Valli; P Sergi; M Moggio; G Scarlato
Journal:  Ital J Neurol Sci       Date:  1980-03
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.