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No to Shinkei = Brain and Nerve
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October 1, 1996
[P300 findings in patients with corticobasal degeneration]
A Homma, H Harayama, H Kondo, et al.
The Journal of Biological Chemistry
|
June 3, 1994
Expression cloning of a GM3-specific alpha-2,8-sialyltransferase (GD3 synthase)
K Sasaki, K Kurata, N Kojima, et al.
Neurology
|
March 1, 1994
Familial juvenile parkinsonism: clinical and pathologic study in a family
H Takahashi, E Ohama, S Suzuki, et al.
Journal of Neuroscience Research
|
May 7, 2002
Time course of polyglutamine aggregate body formation and cell death: enhanced growth in nucleus and an interval for cell death
I Toyoshima, M Sugawara, K Kato, et al.
Neurogenetics
|
March 25, 2000
A missense mutation in the SOD1 gene in patients with amyotrophic lateral sclerosis from the Kii Peninsula and its vicinity, Japan
K Kikugawa, R Nakano, T Inuzuka, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
May 3, 2000
[Familial amyotrophic lateral sclerosis associated with mutant Cu/Zn superoxide dismutase as a conformational disease]
T Koide, S Igarashi, K Kikugawa, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
March 27, 2001
[Improvement of method to estimate guidance by pharmacists and trial to obtain standard pharmaceutical management and guidance services program]
T Kubo, M Kaji, S Tsuji, et al.
Human Immunology
|
April 11, 2001
FcgammaRIII b and FcgammaRIIa polymorphism may affect the production of specific NA1 autoantibody and clinical course of autoimmune neutropenia of infancy
S Taniuchi, M Masuda, A Yamamoto, et al.
Annals of Neurology
|
February 1, 1984
Carrier detection of sialidosis with partial beta-galactosidase deficiency by the assay of lysosomal sialidase in lymphocytes
S Tsuji, T Yamada, T Ariga, et al.
Annals of Neurology
|
March 1, 1995
The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q
H Tanaka, K Endo, S Tsuji, et al.
Page
of 99
Search research articles
Search
Showing results (671-680 of 990) with videos related to
Sort By:
Page
of 99
No to Shinkei = Brain and Nerve
|
October 1, 1996
[P300 findings in patients with corticobasal degeneration]
A Homma, H Harayama, H Kondo, et al.
The Journal of Biological Chemistry
|
June 3, 1994
Expression cloning of a GM3-specific alpha-2,8-sialyltransferase (GD3 synthase)
K Sasaki, K Kurata, N Kojima, et al.
Neurology
|
March 1, 1994
Familial juvenile parkinsonism: clinical and pathologic study in a family
H Takahashi, E Ohama, S Suzuki, et al.
Journal of Neuroscience Research
|
May 7, 2002
Time course of polyglutamine aggregate body formation and cell death: enhanced growth in nucleus and an interval for cell death
I Toyoshima, M Sugawara, K Kato, et al.
Neurogenetics
|
March 25, 2000
A missense mutation in the SOD1 gene in patients with amyotrophic lateral sclerosis from the Kii Peninsula and its vicinity, Japan
K Kikugawa, R Nakano, T Inuzuka, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
May 3, 2000
[Familial amyotrophic lateral sclerosis associated with mutant Cu/Zn superoxide dismutase as a conformational disease]
T Koide, S Igarashi, K Kikugawa, et al.
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan
|
March 27, 2001
[Improvement of method to estimate guidance by pharmacists and trial to obtain standard pharmaceutical management and guidance services program]
T Kubo, M Kaji, S Tsuji, et al.
Human Immunology
|
April 11, 2001
FcgammaRIII b and FcgammaRIIa polymorphism may affect the production of specific NA1 autoantibody and clinical course of autoimmune neutropenia of infancy
S Taniuchi, M Masuda, A Yamamoto, et al.
Annals of Neurology
|
February 1, 1984
Carrier detection of sialidosis with partial beta-galactosidase deficiency by the assay of lysosomal sialidase in lymphocytes
S Tsuji, T Yamada, T Ariga, et al.
Annals of Neurology
|
March 1, 1995
The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q
H Tanaka, K Endo, S Tsuji, et al.
Page
of 99