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I Nonaka

Showing results (321-330 of 503) with videos related to

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Annals of Neurology|April 1, 1994
Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)M Tokunaga, S Mita, T Murakami, et al.
Pediatric Neurology|May 1, 1989
Infantile cytochrome c oxidase deficiency with neonatal deathT Takayanagi, M Inoue, K Tomimasu, et al.
Acta Neuropathologica|December 5, 1997
Apoptotic nuclear degeneration in Marinesco-Sjögren syndromeY Suzuki, N Murakami, Y Goto, et al.
Brain & Development|July 1, 1997
Congenital familial myopathy with type 2 fiber hypoplasia and type 1 fiber predominanceH Muranaka, S Osari, H Fujita, et al.
Pediatric Neurology|September 1, 1992
Leigh encephalopathy: histologic and biochemical analyses of muscle biopsiesT Nagai, Y Goto, T Matsuoka, et al.
Annals of Neurology|April 1, 1985
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patientM Zeviani, I Nonaka, E Bonilla, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 22, 2001
[Overloading to neck extensor muscles is an aggravating factor to induce further neck drop in isolated neck extensor myopathy (Katz). A case report]K Oishi, H Shigeto, K Maruyama, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophyJ Chae, N Minami, Y Jin, et al.
Immunogenetics|June 12, 2001
Occurrence of structural specialization of the serine protease domain of complement factor B at the emergence of jawed vertebrates and adaptive immunityT Terado, S L Smith, T Nakanishi, et al.
Biochemical and Biophysical Research Communications|December 30, 1993
Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory functionJ Hayashi, S Ohta, D Takai, et al.
Pageof 51

Showing results (321-330 of 503) with videos related to

Sort By:
Pageof 51
Annals of Neurology|April 1, 1994
Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)M Tokunaga, S Mita, T Murakami, et al.
Pediatric Neurology|May 1, 1989
Infantile cytochrome c oxidase deficiency with neonatal deathT Takayanagi, M Inoue, K Tomimasu, et al.
Acta Neuropathologica|December 5, 1997
Apoptotic nuclear degeneration in Marinesco-Sjögren syndromeY Suzuki, N Murakami, Y Goto, et al.
Brain & Development|July 1, 1997
Congenital familial myopathy with type 2 fiber hypoplasia and type 1 fiber predominanceH Muranaka, S Osari, H Fujita, et al.
Pediatric Neurology|September 1, 1992
Leigh encephalopathy: histologic and biochemical analyses of muscle biopsiesT Nagai, Y Goto, T Matsuoka, et al.
Annals of Neurology|April 1, 1985
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patientM Zeviani, I Nonaka, E Bonilla, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 22, 2001
[Overloading to neck extensor muscles is an aggravating factor to induce further neck drop in isolated neck extensor myopathy (Katz). A case report]K Oishi, H Shigeto, K Maruyama, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophyJ Chae, N Minami, Y Jin, et al.
Immunogenetics|June 12, 2001
Occurrence of structural specialization of the serine protease domain of complement factor B at the emergence of jawed vertebrates and adaptive immunityT Terado, S L Smith, T Nakanishi, et al.
Biochemical and Biophysical Research Communications|December 30, 1993
Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory functionJ Hayashi, S Ohta, D Takai, et al.
Pageof 51