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No to Hattatsu = Brain and Development
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September 16, 1999
[A patient of Walker-Warburg syndrome with a haplotype different from that in Fukuyama-type congenital muscular dystrophy]
M Sasaki, E Kondo, Y Yamashita, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
May 1, 1986
[An autopsy case of congenital myotonic dystrophy in an adult]
H Tomi, M Mukoyama, J Kitamura, et al.
Acta Neuropathologica
|
January 1, 1983
Pathophysiology of muscle fiber necrosis induced by bupivacaine hydrochloride (Marcaine)
I Nonaka, A Takagi, S Ishiura, et al.
Muscle & Nerve
|
September 1, 1983
Malignant hyperthermia and related neuromuscular diseases: caffeine contracture of the skinned muscle fibers
A Takagi, N Sunohara, T Ishihara, et al.
Journal of the Neurological Sciences
|
August 1, 1984
Behavior of sarcotubular system formation in experimentally induced regeneration of muscle fibers
T Miike, I Nonaka, Y Ohtani, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
September 1, 1982
[Staircase phenomenon in "mitochodrial myopathy' and limb-girdle type muscular dystrophy]
N Sunohara, H Tomi, S Tachibana, et al.
Biochemical and Biophysical Research Communications
|
September 15, 1993
Haemopoietic activity associated with biglycan like proteoglycan
I Kamo, A Kikuchi, I Nonaka, et al.
Pediatric Neurology
|
May 1, 1993
Myopathy with abnormal distribution of dystrophin, growth retardation, mental retardation, and hypospadia
T Nagai, Y Tuchiya, A Maruyama, et al.
Brain & Development
|
January 1, 1989
Muscle histochemistry in myotubular (centronuclear) myopathy
T Sasaki, K Shikura, K Sugai, et al.
Annals of Neurology
|
June 1, 1992
A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy
Y Goto, M Tojo, J Tohyama, et al.
Page
of 51
Search research articles
Search
Showing results (171-180 of 503) with videos related to
Sort By:
Page
of 51
No to Hattatsu = Brain and Development
|
September 16, 1999
[A patient of Walker-Warburg syndrome with a haplotype different from that in Fukuyama-type congenital muscular dystrophy]
M Sasaki, E Kondo, Y Yamashita, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
May 1, 1986
[An autopsy case of congenital myotonic dystrophy in an adult]
H Tomi, M Mukoyama, J Kitamura, et al.
Acta Neuropathologica
|
January 1, 1983
Pathophysiology of muscle fiber necrosis induced by bupivacaine hydrochloride (Marcaine)
I Nonaka, A Takagi, S Ishiura, et al.
Muscle & Nerve
|
September 1, 1983
Malignant hyperthermia and related neuromuscular diseases: caffeine contracture of the skinned muscle fibers
A Takagi, N Sunohara, T Ishihara, et al.
Journal of the Neurological Sciences
|
August 1, 1984
Behavior of sarcotubular system formation in experimentally induced regeneration of muscle fibers
T Miike, I Nonaka, Y Ohtani, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
September 1, 1982
[Staircase phenomenon in "mitochodrial myopathy' and limb-girdle type muscular dystrophy]
N Sunohara, H Tomi, S Tachibana, et al.
Biochemical and Biophysical Research Communications
|
September 15, 1993
Haemopoietic activity associated with biglycan like proteoglycan
I Kamo, A Kikuchi, I Nonaka, et al.
Pediatric Neurology
|
May 1, 1993
Myopathy with abnormal distribution of dystrophin, growth retardation, mental retardation, and hypospadia
T Nagai, Y Tuchiya, A Maruyama, et al.
Brain & Development
|
January 1, 1989
Muscle histochemistry in myotubular (centronuclear) myopathy
T Sasaki, K Shikura, K Sugai, et al.
Annals of Neurology
|
June 1, 1992
A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy
Y Goto, M Tojo, J Tohyama, et al.
Page
of 51