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Acta Neuropathologica|January 1, 1993
Nephrosialidosis: ultrastructural and lectin histochemical studyK Toyooka, H Fujimura, H Yoshikawa, et al.Journal of the Neurological Sciences|August 1, 1995
Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNA(Ile) 4269 mutation): histochemical, immunohistochemical, and ultrastructural studyM Kaido, H Fujimura, M Taniike, et al.Acta Neuropathologica|September 1, 1996
Alzheimer-type pathology in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)M Kaido, H Fujimura, F Soga, et al.Acta Neuropathologica|January 1, 1995
Familial amyloid polyneuropathy associated with transthyretin Gly42 mutation: a quantitative light and electron microscopic study of the peripheral nervous systemK Toyooka, H Fujimura, S Ueno, et al.Rinsho Shinkeigaku = Clinical Neurology|November 1, 1989
[A case of facioscapulohumeral muscular dystrophy with sensorineural hearing loss and retinal angioma]H Fujimura, H Yoshikawa, S Ueno, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1995
Eyelid "apraxia" in patients with motor neuron diseaseK Abe, H Fujimura, C Tatsumi, et al.Journal of the Neurological Sciences|May 1, 1997
Cognitive function in amyotrophic lateral sclerosisK Abe, H Fujimura, K Toyooka, et al.Journal of the Neurological Sciences|December 20, 1994
Involvement of the central nervous system in myotonic dystrophyK Abe, H Fujimura, K Toyooka, et al.Brain : a Journal of Neurology|October 1, 1992
Familial amyloid polyneuropathy associated with the transthyretin Cys114 gene in a Japanese kindredS Ueno, H Fujimura, S Yorifuji, et al.Neurology|August 1, 1993
Single-photon emission computed tomographic investigation of patients with motor neuron diseaseK Abe, H Fujimura, K Toyooka, et al.Pageof 358