Hirano bodies in the axon of peripheral nerves in a case with progressive external ophthalmoplegia with multisystemic involvements
暂无分享,去创建一个
[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 .