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Journal of the Neurological Sciences
|
September 1, 1989
Tissue specificity in cytochrome c oxidase deficient myopathy
I Nonaka, Y Koga, E Ohtaki, et al.
The Kumamoto Medical Journal
|
June 30, 1975
Ultrastructural changes in the cerebellum of young rats having received diphenylhydantoin during the embryonal stage
Y Origuchi, I Nonaka, T Ueno, et al.
Journal of Neuroscience Research
|
August 1, 1988
Localization of ingensin in rat central nervous system and skeletal muscle
K Kamakura, S Ishiura, I Nonaka, et al.
Acta Neuropathologica
|
May 20, 1999
Nebulin is normally expressed in nemaline myopathy
C Imoto, S Kimura, M Kawai, et al.
Muscle & Nerve
|
April 1, 1988
alpha-Glucosidase isoenzymes in normal and acid maltase-deficient human skeletal muscles
F Usuki, S Ishiura, I Nonaka, et al.
No to Hattatsu = Brain and Development
|
March 1, 1990
[Case report of neuronal ceroid lipofuscinosis: muscle biopsy and TRH treatment]
H Iwasaki, K Sugai, N Sakuragawa, et al.
Neuromuscular Disorders : NMD
|
January 1, 1991
Muscle coenzyme Q10 in mitochondrial encephalomyopathies
T Matsuoka, H Maeda, Y Goto, et al.
Journal of Biochemistry
|
January 1, 1980
Calcium-activated neutral protease. Its localization in the myofibril, especially at the Z-band
S Ishiura, H Sugita, I Nonaka, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)
S Tsujino, S Shanske, I Nonaka, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
October 1, 1994
[A patient of late-onset nemaline myopathy with mononuclear cell infiltration]
H Miura, K Kannari, H Kashiwamura, et al.
Page
of 51
Search research articles
Search
Showing results (111-120 of 503) with videos related to
Sort By:
Page
of 51
Journal of the Neurological Sciences
|
September 1, 1989
Tissue specificity in cytochrome c oxidase deficient myopathy
I Nonaka, Y Koga, E Ohtaki, et al.
The Kumamoto Medical Journal
|
June 30, 1975
Ultrastructural changes in the cerebellum of young rats having received diphenylhydantoin during the embryonal stage
Y Origuchi, I Nonaka, T Ueno, et al.
Journal of Neuroscience Research
|
August 1, 1988
Localization of ingensin in rat central nervous system and skeletal muscle
K Kamakura, S Ishiura, I Nonaka, et al.
Acta Neuropathologica
|
May 20, 1999
Nebulin is normally expressed in nemaline myopathy
C Imoto, S Kimura, M Kawai, et al.
Muscle & Nerve
|
April 1, 1988
alpha-Glucosidase isoenzymes in normal and acid maltase-deficient human skeletal muscles
F Usuki, S Ishiura, I Nonaka, et al.
No to Hattatsu = Brain and Development
|
March 1, 1990
[Case report of neuronal ceroid lipofuscinosis: muscle biopsy and TRH treatment]
H Iwasaki, K Sugai, N Sakuragawa, et al.
Neuromuscular Disorders : NMD
|
January 1, 1991
Muscle coenzyme Q10 in mitochondrial encephalomyopathies
T Matsuoka, H Maeda, Y Goto, et al.
Journal of Biochemistry
|
January 1, 1980
Calcium-activated neutral protease. Its localization in the myofibril, especially at the Z-band
S Ishiura, H Sugita, I Nonaka, et al.
Muscle & Nerve. Supplement
|
January 1, 1995
The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)
S Tsujino, S Shanske, I Nonaka, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
October 1, 1994
[A patient of late-onset nemaline myopathy with mononuclear cell infiltration]
H Miura, K Kannari, H Kashiwamura, et al.
Page
of 51