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The Journal of Pediatrics|January 1, 1992
Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) geneK Inui, H Fukushima, H Tsukamoto, et al.Acta Neuropathologica|January 1, 1993
Nephrosialidosis: ultrastructural and lectin histochemical studyK Toyooka, H Fujimura, H Yoshikawa, et al.Journal of Child Neurology|July 5, 2007
Neuronal intranuclear hyaline inclusion disease with rapidly progressive neurological symptomsT Mano, S Takizawa, I Mohri, et al.American Journal of Medical Genetics|July 1, 1993
Case of ring chromosome 7: the first report of neuropathological findingsH Tsukamoto, N Sakai, M Taniike, et al.Cell|August 26, 1994
Absence of MHC class II molecules reduces CNS demyelination, microglial/macrophage infiltration, and twitching in murine globoid cell leukodystrophyG K Matsushima, M Taniike, L H Glimcher, et al.Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs diseaseS Yamanaka, M D Johnson, A Grinberg, 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.Heart (British Cardiac Society)|April 16, 2005
Acute myocardial infarction caused by a septic coronary embolism diagnosed and treated with a thrombectomy catheterM Taniike, M Nishino, Y Egami, et al.Brain & Development|July 1, 1992
A case of Hallervorden-Spatz disease: progressive and intractable dystonia controlled by bilateral thalamotomyH Tsukamoto, K Inui, M Taniike, et al.Human Molecular Genetics|October 1, 1995
Molecular defects in Krabbe diseaseN Tatsumi, K Inui, N Sakai, et al.Pageof 4