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I Nonaka

Showing results (201-210 of 503) with videos related to

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Rinsho Shinkeigaku = Clinical Neurology|June 1, 1980
[Two cases of subclinical myopathy. Is it a trait for malignant hyperthermia? (author's transl)]N Sunohara, A Takagi, I Nonaka, et al.
Journal of the Neurological Sciences|October 1, 1986
High AMP deaminase activity in rimmed vacuoles of skeletal muscleI Higuchi, I Nonaka, S Ishiura, et al.
Brain & Development|May 1, 1992
Infantile polymyositis: a case reportT Nagai, T Hasegawa, M Saito, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 1, 1990
[Mitochondrial encephalomyopathy (focal cytochrome c oxidase deficiency) with transient episodes of muscle weakness and elevation of serum creatine kinase activity]M Ohno, T Kobayashi, K Tanaka, et al.
Biochemical and Biophysical Research Communications|August 15, 1994
A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)Y Goto, K Tsugane, Y Tanabe, et al.
Neurology|March 1, 1996
Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive formO Kobayashi, Y Hayashi, K Arahata, et al.
Immunology|May 1, 1993
Characterization of a macrophage lineage cell colony-stimulating factor produced by thymic myoid cellsI Kamo, T Kunishita, A Kikuchi, et al.
Journal of the Neurological Sciences|September 1, 1991
Immunocytochemical analysis of dystrophin in congenital muscular dystrophyE Arikawa, T Ishihara, I Nonaka, et al.
Rinsho Shinkeigaku = Clinical Neurology|January 5, 2002
[A patient with dermatomyositis and systemic sclerosis with preferential facioscapulohumeral muscle involvement and fatal cardiomyopathy]Y Oya, J Toyama, M Ogawa, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 1, 1990
[Cardiomyopathy in Becker muscular dystrophy]C Sakata, H Yamada, N Sunohara, et al.
Pageof 51

Showing results (201-210 of 503) with videos related to

Sort By:
Pageof 51
Rinsho Shinkeigaku = Clinical Neurology|June 1, 1980
[Two cases of subclinical myopathy. Is it a trait for malignant hyperthermia? (author's transl)]N Sunohara, A Takagi, I Nonaka, et al.
Journal of the Neurological Sciences|October 1, 1986
High AMP deaminase activity in rimmed vacuoles of skeletal muscleI Higuchi, I Nonaka, S Ishiura, et al.
Brain & Development|May 1, 1992
Infantile polymyositis: a case reportT Nagai, T Hasegawa, M Saito, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 1, 1990
[Mitochondrial encephalomyopathy (focal cytochrome c oxidase deficiency) with transient episodes of muscle weakness and elevation of serum creatine kinase activity]M Ohno, T Kobayashi, K Tanaka, et al.
Biochemical and Biophysical Research Communications|August 15, 1994
A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)Y Goto, K Tsugane, Y Tanabe, et al.
Neurology|March 1, 1996
Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive formO Kobayashi, Y Hayashi, K Arahata, et al.
Immunology|May 1, 1993
Characterization of a macrophage lineage cell colony-stimulating factor produced by thymic myoid cellsI Kamo, T Kunishita, A Kikuchi, et al.
Journal of the Neurological Sciences|September 1, 1991
Immunocytochemical analysis of dystrophin in congenital muscular dystrophyE Arikawa, T Ishihara, I Nonaka, et al.
Rinsho Shinkeigaku = Clinical Neurology|January 5, 2002
[A patient with dermatomyositis and systemic sclerosis with preferential facioscapulohumeral muscle involvement and fatal cardiomyopathy]Y Oya, J Toyama, M Ogawa, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 1, 1990
[Cardiomyopathy in Becker muscular dystrophy]C Sakata, H Yamada, N Sunohara, et al.
Pageof 51