Search research articles
Contact Us
Filters
Showing results (91-100 of 178) with videos related to
Page
of 18
Sort By:
Anticancer Research
|
May 1, 1987
The effect of a biological response modifier, PSK, on the intestinal immune system in tumor-bearing mice
K Matsunaga, I Morita, Y Oguchi, et al.
American Journal of Ophthalmology
|
February 1, 1995
Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy
Y Mashima, Y Hiida, M Saga, et al.
Nippon Ganka Gakkai Zasshi
|
August 10, 1977
[Effect of glucocorticoid on the developing retinal vessels of the rabbit (author's transl)]
S Akiya, Y Uemura, H Yokoyama, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
June 1, 1997
High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation
K Yamada, Y Mashima, K Kigasawa, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 22, 1998
Orbital high resolution magnetic resonance imaging with fast spin echo in the acute stage of Leber's hereditary optic neuropathy
Y Mashima, K Oshitari, Y Imamura, et al.
The British Journal of Ophthalmology
|
December 9, 2003
Scanning laser Doppler flowmeter study of retinal blood flow in macular area of healthy volunteers
I Kimura, K Shinoda, T Tanino, et al.
Investigative Ophthalmology & Visual Science
|
June 14, 2000
Coexpression of VEGF receptors VEGF-R2 and neuropilin-1 in proliferative diabetic retinopathy
S Ishida, K Shinoda, S Kawashima, et al.
American Journal of Ophthalmology
|
December 15, 1993
DNA diagnosis of Leber's hereditary optic neuropathy by using dried blood specimens
Y Mashima, Y Hiida, R Kubota, et al.
Human Genetics
|
November 1, 1993
A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa
M Saga, Y Mashima, K Akeo, et al.
Ophthalmic Genetics
|
June 1, 1994
Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese family
M Saga, Y Mashima, K Akeo, et al.
Page
of 18
Search research articles
Search
Showing results (91-100 of 178) with videos related to
Sort By:
Page
of 18
Anticancer Research
|
May 1, 1987
The effect of a biological response modifier, PSK, on the intestinal immune system in tumor-bearing mice
K Matsunaga, I Morita, Y Oguchi, et al.
American Journal of Ophthalmology
|
February 1, 1995
Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy
Y Mashima, Y Hiida, M Saga, et al.
Nippon Ganka Gakkai Zasshi
|
August 10, 1977
[Effect of glucocorticoid on the developing retinal vessels of the rabbit (author's transl)]
S Akiya, Y Uemura, H Yokoyama, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
June 1, 1997
High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation
K Yamada, Y Mashima, K Kigasawa, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 22, 1998
Orbital high resolution magnetic resonance imaging with fast spin echo in the acute stage of Leber's hereditary optic neuropathy
Y Mashima, K Oshitari, Y Imamura, et al.
The British Journal of Ophthalmology
|
December 9, 2003
Scanning laser Doppler flowmeter study of retinal blood flow in macular area of healthy volunteers
I Kimura, K Shinoda, T Tanino, et al.
Investigative Ophthalmology & Visual Science
|
June 14, 2000
Coexpression of VEGF receptors VEGF-R2 and neuropilin-1 in proliferative diabetic retinopathy
S Ishida, K Shinoda, S Kawashima, et al.
American Journal of Ophthalmology
|
December 15, 1993
DNA diagnosis of Leber's hereditary optic neuropathy by using dried blood specimens
Y Mashima, Y Hiida, R Kubota, et al.
Human Genetics
|
November 1, 1993
A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa
M Saga, Y Mashima, K Akeo, et al.
Ophthalmic Genetics
|
June 1, 1994
Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese family
M Saga, Y Mashima, K Akeo, et al.
Page
of 18