Hirano bodies in the axon of peripheral nerves in a case with progressive external ophthalmoplegia with multisystemic involvements

[1]  J. Beal Morphogenesis of the Hirano body in neurons of the squirrel monkey dorsal horn , 1978, Journal of neurocytology.

[2]  S. Dimauro,et al.  Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome? , 1977, Annals of neurology.

[3]  H. M. Dembitzer,et al.  EOSINOPHILIC ROD‐LIKE STRUCTURES IN MYELINATED FIBERS OF HAMSTER SPINAL ROOTS , 1976 .

[4]  A. Anzil,et al.  Rod-shaped filamentous inclusions and other ultrastructural features in a cerebellar astrocytoma , 1975, Acta Neuropathologica.

[5]  M. Hadfield,et al.  Progressive multifocal leukoencephalopathy with paramyxovirus-like structures, Hirano bodies and neurofibrillary tangles , 1974, Acta Neuropathologica.

[6]  D. McFarlin,et al.  Session on Neuromuscular Diseases , 1973, Neurology.

[7]  E. Fisher,et al.  Unique, concentrically laminated, membranous inclusions in myofibers. , 1972, American journal of clinical pathology.

[8]  W. Engel,et al.  Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers: Histochemical and Ultrastructural Changes in Limb Muscles of a Group of Patients With Idiopathic Progressive External Ophthalmoplegia , 1972 .

[9]  J. Hassoun,et al.  Un cas de dystrophie neuroaxonale infantile ou maladie de Seitelberger , 1971, Acta Neuropathologica.

[10]  J. Cavanagh,et al.  Fibrillary accumulations in oligodendroglial processes of rats subjected to portocaval anastomosis , 1971 .

[11]  E. J. Field,et al.  Electron microscopic observations on the cerebellar cortex in kuru. , 1969, Journal of the neurological sciences.

[12]  L. Kurland,et al.  THE FINE STRUCTURE OF SOME INTRAGANGLIONIC ALTERATIONS , 1968 .

[13]  N. Gonatas A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome. II. Ultrastructure. , 1967, The American journal of medicine.

[14]  L. Kurland,et al.  Amyotrophic lateral sclerosis and Parkinsonism-dementia complex on Guam. Further pathologic studies. , 1966, Archives of neurology.

[15]  G. Glaser,et al.  Spongiform encephalopathy with chronic progressive external ophthalmoplegia , 1966, Neurology.

[16]  Y. Takei Infantile neuroaxonal dystrophy (Seitelberger's disease) , 1965, Acta Neuropathologica.

[17]  L. Ernster,et al.  A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study. , 1962, The Journal of clinical investigation.

[18]  H. Fred,et al.  Occurrence of retinal pigmentation, ophthalmoplegia, ataxia, deafness and heart block. Report of a case, with findings at autopsy. , 1960, The American journal of medicine.

[19]  G. P. Sayre,et al.  Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases. , 1958, A M A Archives of Ophthalmology.

[20]  S. Schochet,et al.  Ultrastructure of Hirano bodies , 2004, Acta Neuropathologica.

[21]  H. Cravioto,et al.  A study of rod-like structures (Hirano bodies) in 240 normal and pathological brains , 2004, Acta Neuropathologica.

[22]  S. Yagishita,et al.  Infantile neuroaxonal dystrophy , 2004, Acta Neuropathologica.

[23]  W. Engel,et al.  Oculocraniosomatic neuromuscular disease with "ragged-red" fibers. , 1972, Archives of neurology.

[24]  J. Hassoun,et al.  [Infantile neuroaxonal dystrophy or Seitelberger's disease. 3. Ultrastructural study of striated muscle]. , 1971, Acta neuropathologica.

[25]  W. Villiger,et al.  Elektronenmikroskopische Befunde bei 3 Fllen von chronisch progressiver okulrer Muskeldystrophie , 1967 .