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The Kumamoto Medical Journal
|
June 30, 1972
An electron microscopical study of the muscle in congenital muscular dystrophy
I Nonaka, S Miyoshino, T Miike, et al.
Acta Neuropathologica
|
October 1, 1998
Fiber-type-dependent expression of adenovirus-mediated transgene in mouse skeletal muscle fibers
Y Hagiwara, A Ishii, I Nonaka, et al.
Journal of Neurology
|
January 1, 1985
Two siblings with multiple intracranial haemangiomatosis with calcification
A Tateno, A Matsui, N Sakuragawa, et al.
Muscle & Nerve
|
December 18, 2001
A new form of muscular dystrophy with mitochondrial structural abnormalities
K Ikemoto-Tsuchiya, I Nishino, M Kawai, et al.
Muscle & Nerve
|
March 1, 1997
Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families
M Ozawa, I Nishino, S Horai, et al.
Neurology
|
January 28, 2009
Novel FHL1 mutations in fatal and benign reducing body myopathy
S Shalaby, Y K Hayashi, I Nonaka, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
March 20, 2001
Novel androgen-dependent promoters direct expression of the C4b-binding protein alpha-chain gene in epididymis
M I Nonaka, G Wang, T Mori, et al.
Chemical & Pharmaceutical Bulletin
|
April 20, 2001
Revised structure of cercidinin A, a novel ellagitannin having (R)-hexahydroxydiphenoyl esters at the 3,4-positions of glucopyranose
T Tanaka, G I Nonaka, M Ishimatsu, et al.
Acta Neuropathologica
|
January 1, 1995
Reducing bodies in distal myopathy with rimmed vacuole formation
B H Kiyomoto, N Murakami, J Kishibayashi, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
April 1, 1989
[Ultrastructural immunocytochemical localization of electron-transport enzymes in mitochondrial myopathy]
D L Song, T Sato, H Ujike, et al.
Page
of 51
Search research articles
Search
Showing results (241-250 of 503) with videos related to
Sort By:
Page
of 51
The Kumamoto Medical Journal
|
June 30, 1972
An electron microscopical study of the muscle in congenital muscular dystrophy
I Nonaka, S Miyoshino, T Miike, et al.
Acta Neuropathologica
|
October 1, 1998
Fiber-type-dependent expression of adenovirus-mediated transgene in mouse skeletal muscle fibers
Y Hagiwara, A Ishii, I Nonaka, et al.
Journal of Neurology
|
January 1, 1985
Two siblings with multiple intracranial haemangiomatosis with calcification
A Tateno, A Matsui, N Sakuragawa, et al.
Muscle & Nerve
|
December 18, 2001
A new form of muscular dystrophy with mitochondrial structural abnormalities
K Ikemoto-Tsuchiya, I Nishino, M Kawai, et al.
Muscle & Nerve
|
March 1, 1997
Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families
M Ozawa, I Nishino, S Horai, et al.
Neurology
|
January 28, 2009
Novel FHL1 mutations in fatal and benign reducing body myopathy
S Shalaby, Y K Hayashi, I Nonaka, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
March 20, 2001
Novel androgen-dependent promoters direct expression of the C4b-binding protein alpha-chain gene in epididymis
M I Nonaka, G Wang, T Mori, et al.
Chemical & Pharmaceutical Bulletin
|
April 20, 2001
Revised structure of cercidinin A, a novel ellagitannin having (R)-hexahydroxydiphenoyl esters at the 3,4-positions of glucopyranose
T Tanaka, G I Nonaka, M Ishimatsu, et al.
Acta Neuropathologica
|
January 1, 1995
Reducing bodies in distal myopathy with rimmed vacuole formation
B H Kiyomoto, N Murakami, J Kishibayashi, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
April 1, 1989
[Ultrastructural immunocytochemical localization of electron-transport enzymes in mitochondrial myopathy]
D L Song, T Sato, H Ujike, et al.
Page
of 51