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Rinsho Shinkeigaku = Clinical Neurology
|
February 1, 1990
[A case of Becker muscular dystrophy presenting cardiac failure as an initial symptom]
C Sakata, N Sunohara, I Nonaka, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
July 8, 2000
[Lysosomal glycogen storage disease with normal acid maltase (Danon) without apparent cardiomyopathy and mental retardation]
H Kawamura, S Shimojo, I Nonaka, et al.
Journal of Human Genetics
|
February 24, 2001
Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene
J Akanuma, K Muraki, H Komaki, et al.
Brain & Development
|
March 1, 1994
Scoliosis associated with central core disease
T Nagai, Y Tsuchiya, A Maruyama, et al.
Human Molecular Genetics
|
June 1, 1994
Two mutations, one novel and one frequently observed, in Japanese patients with McArdle's disease
S Tsujino, S Shanske, Y Goto, et al.
Journal of Neuropathology and Experimental Neurology
|
September 1, 1984
6-Aminonicotinamide-induced hydrocephalus in suckling mice
H Aikawa, K Suzuki, N Ito, et al.
Journal of Electron Microscopy
|
January 1, 1986
High resolution freeze replica by means of high melting point metal shadowing
H Akahori, Y Nakajima, K Terasawa, et al.
Acta Neuropathologica
|
January 1, 1988
Variability in the activity of respiratory chain enzymes in mitochondrial myopathies
Y Koga, I Nonaka, N Sunohara, et al.
Brain & Development
|
March 1, 1992
Congenital focal muscle dysplasia in the lower extremities from probable abnormal innervation: a case report
H Yamanouchi, I Nonaka, M Kaga, et al.
Acta Neuropathologica
|
January 1, 1987
Acid maltase deficiency in the Japanese quail; early morphological event in skeletal muscle
I Higuchi, I Nonaka, F Usuki, et al.
Page
of 51
Search research articles
Search
Showing results (211-220 of 503) with videos related to
Sort By:
Page
of 51
Rinsho Shinkeigaku = Clinical Neurology
|
February 1, 1990
[A case of Becker muscular dystrophy presenting cardiac failure as an initial symptom]
C Sakata, N Sunohara, I Nonaka, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
July 8, 2000
[Lysosomal glycogen storage disease with normal acid maltase (Danon) without apparent cardiomyopathy and mental retardation]
H Kawamura, S Shimojo, I Nonaka, et al.
Journal of Human Genetics
|
February 24, 2001
Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene
J Akanuma, K Muraki, H Komaki, et al.
Brain & Development
|
March 1, 1994
Scoliosis associated with central core disease
T Nagai, Y Tsuchiya, A Maruyama, et al.
Human Molecular Genetics
|
June 1, 1994
Two mutations, one novel and one frequently observed, in Japanese patients with McArdle's disease
S Tsujino, S Shanske, Y Goto, et al.
Journal of Neuropathology and Experimental Neurology
|
September 1, 1984
6-Aminonicotinamide-induced hydrocephalus in suckling mice
H Aikawa, K Suzuki, N Ito, et al.
Journal of Electron Microscopy
|
January 1, 1986
High resolution freeze replica by means of high melting point metal shadowing
H Akahori, Y Nakajima, K Terasawa, et al.
Acta Neuropathologica
|
January 1, 1988
Variability in the activity of respiratory chain enzymes in mitochondrial myopathies
Y Koga, I Nonaka, N Sunohara, et al.
Brain & Development
|
March 1, 1992
Congenital focal muscle dysplasia in the lower extremities from probable abnormal innervation: a case report
H Yamanouchi, I Nonaka, M Kaga, et al.
Acta Neuropathologica
|
January 1, 1987
Acid maltase deficiency in the Japanese quail; early morphological event in skeletal muscle
I Higuchi, I Nonaka, F Usuki, et al.
Page
of 51