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K Sahashi

Showing results (71-80 of 96) with videos related to

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Archives of Neurology|May 1, 1983
Amyotrophic lateral sclerosis. Lack of central chromatolytic response of motor neurocytons corresponding to active axonal degenerationG Sobue, Y Hashizume, K Sahashi, et al.
Acta Neuropathologica|January 1, 1985
Immunohistochemical demonstration of carbonic anhydrase III and muscle-specific enolase in paraffin-embedded human skeletal muscle sectionsT Ibi, H Haimoto, H Nagura, et al.
Nihon Kyobu Shikkan Gakkai Zasshi|July 1, 1990
[Echo guided percutaneous needle biopsy for diagnosis of thoracic lesions]S Ito, K Shima, K Sahashi, et al.
Internal Medicine (Tokyo, Japan)|May 1, 1994
Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathiesK Sahashi, T Ibi, H Suoh, et al.
Nihon Kyobu Shikkan Gakkai Zasshi|February 1, 1994
[Levels of soluble CD4 and soluble CD8 in patients with sarcoidosis]S Sato, Y Ina, K Takada, et al.
Neurology|February 1, 1979
Passively transferred experimental autoimmune myasthenia gravis. Sequential and quantitative study of the motor end-plate fine structure and ultrastructural localization of immune complexes (IgG and C3), and of the acetylcholine receptorA G Engel, H Sakakibara, K Sahashi, et al.
Journal of the Neurological Sciences|February 1, 1994
Multiplicity of abnormal dystrophin in Becker muscular dystrophy. A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophinS Hori, S Ohtani, T Shimizu, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|February 1, 1991
[Myoglobinuria caused by multiple deletions of mitochondrial DNA]M Tanaka, K Ohno, K Sahashi, et al.
Annals of Neurology|April 1, 1991
Mitochondrial DNA deletions in inherited recurrent myoglobinuriaK Ohno, M Tanaka, K Sahashi, et al.
Brain : a Journal of Neurology|August 1, 1990
Type I familial amyloid polyneuropathy. A pathological study of the peripheral nervous systemG Sobue, N Nakao, K Murakami, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Archives of Neurology|May 1, 1983
Amyotrophic lateral sclerosis. Lack of central chromatolytic response of motor neurocytons corresponding to active axonal degenerationG Sobue, Y Hashizume, K Sahashi, et al.
Acta Neuropathologica|January 1, 1985
Immunohistochemical demonstration of carbonic anhydrase III and muscle-specific enolase in paraffin-embedded human skeletal muscle sectionsT Ibi, H Haimoto, H Nagura, et al.
Nihon Kyobu Shikkan Gakkai Zasshi|July 1, 1990
[Echo guided percutaneous needle biopsy for diagnosis of thoracic lesions]S Ito, K Shima, K Sahashi, et al.
Internal Medicine (Tokyo, Japan)|May 1, 1994
Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathiesK Sahashi, T Ibi, H Suoh, et al.
Nihon Kyobu Shikkan Gakkai Zasshi|February 1, 1994
[Levels of soluble CD4 and soluble CD8 in patients with sarcoidosis]S Sato, Y Ina, K Takada, et al.
Neurology|February 1, 1979
Passively transferred experimental autoimmune myasthenia gravis. Sequential and quantitative study of the motor end-plate fine structure and ultrastructural localization of immune complexes (IgG and C3), and of the acetylcholine receptorA G Engel, H Sakakibara, K Sahashi, et al.
Journal of the Neurological Sciences|February 1, 1994
Multiplicity of abnormal dystrophin in Becker muscular dystrophy. A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophinS Hori, S Ohtani, T Shimizu, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|February 1, 1991
[Myoglobinuria caused by multiple deletions of mitochondrial DNA]M Tanaka, K Ohno, K Sahashi, et al.
Annals of Neurology|April 1, 1991
Mitochondrial DNA deletions in inherited recurrent myoglobinuriaK Ohno, M Tanaka, K Sahashi, et al.
Brain : a Journal of Neurology|August 1, 1990
Type I familial amyloid polyneuropathy. A pathological study of the peripheral nervous systemG Sobue, N Nakao, K Murakami, et al.
Pageof 10