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M Kohda

Showing results (41-50 of 50) with videos related to

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Journal of Cardiography|March 1, 1985
[Exercise echocardiography to evaluate left ventricular function in mitral and aortic regurgitation]K Nishida, H Kitamura, M Higami, et al.
Human Molecular Genetics|February 7, 2001
Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genesM Meguro, K Mitsuya, N Nomura, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine|June 1, 1985
[Evaluation of postextrasystolic potentiation by gated radionuclide ventriculography]H Sugihara, H Adachi, H Nakagawa, et al.
Nihon Sanka Fujinka Gakkai Zasshi|December 1, 1989
[Result of registration and follow-up system of gestational trophoblastic disease in Shizuoka Prefecture (from 1977 to 1988)--recent trend and choriocarcinoma following term gestation]M Maeda, M Sugimura, T Kobayashi, et al.
Dermatology (Basel, Switzerland)|March 13, 2001
Antidesmoglein autoantibodies in silicosis patients with no bullous diseasesH Ueki, M Kohda, T Nobutoh, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine|May 1, 1985
[Detection and evaluation of left atrial myxoma by gated radionuclide imaging]H Sugihara, H Adachi, H Nakagawa, et al.
Journal of Cardiography|September 1, 1986
[Left ventricular systolic performance during exercise in patients with hypertrophic cardiomyopathy]H Kitamura, K Furukawa, T Ebizawa, et al.
Nihon Jinzo Gakkai Shi|June 1, 1982
[Irregular isoantibodies in the sera of patients undergoing chronic hemodialysis]S Katoh, N Maebo, M Kohda, et al.
Biochimica Et Biophysica Acta|January 28, 2014
Diagnosis and molecular basis of mitochondrial respiratory chain disorders: exome sequencing for disease gene identificationA Ohtake, K Murayama, M Mori, et al.
Clinical Genetics|June 16, 2016
DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burstK Zaha, H Matsumoto, M Itoh, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Journal of Cardiography|March 1, 1985
[Exercise echocardiography to evaluate left ventricular function in mitral and aortic regurgitation]K Nishida, H Kitamura, M Higami, et al.
Human Molecular Genetics|February 7, 2001
Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genesM Meguro, K Mitsuya, N Nomura, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine|June 1, 1985
[Evaluation of postextrasystolic potentiation by gated radionuclide ventriculography]H Sugihara, H Adachi, H Nakagawa, et al.
Nihon Sanka Fujinka Gakkai Zasshi|December 1, 1989
[Result of registration and follow-up system of gestational trophoblastic disease in Shizuoka Prefecture (from 1977 to 1988)--recent trend and choriocarcinoma following term gestation]M Maeda, M Sugimura, T Kobayashi, et al.
Dermatology (Basel, Switzerland)|March 13, 2001
Antidesmoglein autoantibodies in silicosis patients with no bullous diseasesH Ueki, M Kohda, T Nobutoh, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine|May 1, 1985
[Detection and evaluation of left atrial myxoma by gated radionuclide imaging]H Sugihara, H Adachi, H Nakagawa, et al.
Journal of Cardiography|September 1, 1986
[Left ventricular systolic performance during exercise in patients with hypertrophic cardiomyopathy]H Kitamura, K Furukawa, T Ebizawa, et al.
Nihon Jinzo Gakkai Shi|June 1, 1982
[Irregular isoantibodies in the sera of patients undergoing chronic hemodialysis]S Katoh, N Maebo, M Kohda, et al.
Biochimica Et Biophysica Acta|January 28, 2014
Diagnosis and molecular basis of mitochondrial respiratory chain disorders: exome sequencing for disease gene identificationA Ohtake, K Murayama, M Mori, et al.
Clinical Genetics|June 16, 2016
DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burstK Zaha, H Matsumoto, M Itoh, et al.
Pageof 5