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Human Genetics
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August 1, 1993
High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy
Y Mashima, Y Hiida, Y Oguchi, et al.
Current Eye Research
|
June 13, 2001
Clinical application of the multifocal VEPs
Y Betsuin, Y Mashima, H Ohde, et al.
Nippon Ganka Gakkai Zasshi
|
May 2, 2001
[Objective evaluation of visual field loss in a patient with branch retinal artery occlusion and brain infarction]
K Yamada, H Ohde, K Shinoda, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine
|
April 1, 1987
[An evaluation of shunt flow by the 133Xe clearance method and admittance plethysmography]
K Kawakami, Y Mori, Y Mashima, et al.
American Journal of Ophthalmology
|
September 23, 1998
The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients
M Konishi, Y Mashima, M Yamada, et al.
Nihon Geka Gakkai Zasshi
|
February 1, 1992
[Adequate requirements of energy and protein in postoperative total parenteral nutrition]
Y Fujisaki, T Tashiro, Y Mashima, et al.
Investigative Ophthalmology & Visual Science
|
April 16, 1998
Transforming growth factor-beta 1 promotes contraction of collagen gel by bovine corneal fibroblasts through differentiation of myofibroblasts
H Kurosaka, D Kurosaka, K Kato, et al.
[Kango Gijutsu] : [Nursing Technique]
|
September 1, 1981
[An innovation in bedpans for unassisted urination--an example with a patient with rheumatoid arthritis who has been unable to walk for the past 35 years]
F Kamata, H Kanda, Y Mashima, et al.
Cornea
|
December 13, 1997
Granular-lattice (Avellino) corneal dystrophy in Japanese patients
M Konishi, Y Mashima, Y Nakamura, et al.
Current Eye Research
|
May 1, 1997
Fluorophotometric measurement of pH of human tears in vivo
M Yamada, H Mochizuki, M Kawai, et al.
Page
of 20
Search research articles
Search
Showing results (91-100 of 199) with videos related to
Sort By:
Page
of 20
Human Genetics
|
August 1, 1993
High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy
Y Mashima, Y Hiida, Y Oguchi, et al.
Current Eye Research
|
June 13, 2001
Clinical application of the multifocal VEPs
Y Betsuin, Y Mashima, H Ohde, et al.
Nippon Ganka Gakkai Zasshi
|
May 2, 2001
[Objective evaluation of visual field loss in a patient with branch retinal artery occlusion and brain infarction]
K Yamada, H Ohde, K Shinoda, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine
|
April 1, 1987
[An evaluation of shunt flow by the 133Xe clearance method and admittance plethysmography]
K Kawakami, Y Mori, Y Mashima, et al.
American Journal of Ophthalmology
|
September 23, 1998
The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients
M Konishi, Y Mashima, M Yamada, et al.
Nihon Geka Gakkai Zasshi
|
February 1, 1992
[Adequate requirements of energy and protein in postoperative total parenteral nutrition]
Y Fujisaki, T Tashiro, Y Mashima, et al.
Investigative Ophthalmology & Visual Science
|
April 16, 1998
Transforming growth factor-beta 1 promotes contraction of collagen gel by bovine corneal fibroblasts through differentiation of myofibroblasts
H Kurosaka, D Kurosaka, K Kato, et al.
[Kango Gijutsu] : [Nursing Technique]
|
September 1, 1981
[An innovation in bedpans for unassisted urination--an example with a patient with rheumatoid arthritis who has been unable to walk for the past 35 years]
F Kamata, H Kanda, Y Mashima, et al.
Cornea
|
December 13, 1997
Granular-lattice (Avellino) corneal dystrophy in Japanese patients
M Konishi, Y Mashima, Y Nakamura, et al.
Current Eye Research
|
May 1, 1997
Fluorophotometric measurement of pH of human tears in vivo
M Yamada, H Mochizuki, M Kawai, et al.
Page
of 20