Search research articles
Contact Us
Filters
Showing results (191-200 of 503) with videos related to
Page
of 51
Sort By:
No to Hattatsu = Brain and Development
|
August 1, 2000
[Two sibling patients with non-Fukuyama type congenital muscular dystrophy with low serum selenium levels--therapeutic effects of oral selenium administration]
M Kurihara, K Kumagai, Y Nakae, et al.
Annals of Neurology
|
December 1, 1988
Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency
Y Koga, I Nonaka, M Kobayashi, et al.
Human Mutation
|
March 27, 1999
Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online
M Ikezawa, I Nishino, Y Goto, et al.
Journal of the Neurological Sciences
|
March 1, 1995
Limb-girdle muscular dystrophy: clinical and pathologic reevaluation
Y Yamanouchi, E Arikawa, K Arahata, et al.
Journal of the Neurological Sciences
|
November 1, 1984
Demonstration of acid alpha-glucosidase in different types of Pompe disease by use of an immunochemical method
N Ninomiya, I Matsuda, T Matsuoka, et al.
Annals of Neurology
|
March 1, 1993
Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
M Tokunaga, S Mita, R Sakuta, et al.
Journal of the Neurological Sciences
|
November 1, 1990
1-[11C]pyruvate turnover in brain and muscle of patients with mitochondrial encephalomyopathy. A study with positron emission tomography (PET)
F Yokoi, T Hara, M Iio, et al.
Internal Medicine (Tokyo, Japan)
|
June 1, 1996
Myotonia congenita with painful muscle cramps
N Sunohara, H Tomi, A Nakamura, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
April 1, 1981
[Two cases with quadriceps myopathy of juvenile onset (author's transl)]
N Sunohara, A Takagi, I Nonaka, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
November 1, 1981
[De Sanctis-Cacchione syndrome: a report of a case and a review of the literature (author's transl)]
O Muramoto, M Mukoyama, I Nonaka, et al.
Page
of 51
Search research articles
Search
Showing results (191-200 of 503) with videos related to
Sort By:
Page
of 51
No to Hattatsu = Brain and Development
|
August 1, 2000
[Two sibling patients with non-Fukuyama type congenital muscular dystrophy with low serum selenium levels--therapeutic effects of oral selenium administration]
M Kurihara, K Kumagai, Y Nakae, et al.
Annals of Neurology
|
December 1, 1988
Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency
Y Koga, I Nonaka, M Kobayashi, et al.
Human Mutation
|
March 27, 1999
Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online
M Ikezawa, I Nishino, Y Goto, et al.
Journal of the Neurological Sciences
|
March 1, 1995
Limb-girdle muscular dystrophy: clinical and pathologic reevaluation
Y Yamanouchi, E Arikawa, K Arahata, et al.
Journal of the Neurological Sciences
|
November 1, 1984
Demonstration of acid alpha-glucosidase in different types of Pompe disease by use of an immunochemical method
N Ninomiya, I Matsuda, T Matsuoka, et al.
Annals of Neurology
|
March 1, 1993
Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
M Tokunaga, S Mita, R Sakuta, et al.
Journal of the Neurological Sciences
|
November 1, 1990
1-[11C]pyruvate turnover in brain and muscle of patients with mitochondrial encephalomyopathy. A study with positron emission tomography (PET)
F Yokoi, T Hara, M Iio, et al.
Internal Medicine (Tokyo, Japan)
|
June 1, 1996
Myotonia congenita with painful muscle cramps
N Sunohara, H Tomi, A Nakamura, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
April 1, 1981
[Two cases with quadriceps myopathy of juvenile onset (author's transl)]
N Sunohara, A Takagi, I Nonaka, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
November 1, 1981
[De Sanctis-Cacchione syndrome: a report of a case and a review of the literature (author's transl)]
O Muramoto, M Mukoyama, I Nonaka, et al.
Page
of 51