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Y Wada

Showing results (811-820 of 982) with videos related to

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Journal of Neurology|July 1, 1988
Peripheral neuropathy with predominantly motor manifestations in a patient with carcinoma of the uterusM Yamada, S Shintani, K Mitani, et al.
Biochemical and Biophysical Research Communications|April 30, 1991
Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's diseaseT Ozawa, M Tanaka, H Ino, et al.
Biochemical and Biophysical Research Communications|January 31, 1991
Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)M Tanaka, H Ino, K Ohno, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1994
Vascular response to vasoactive agents in dialysed patients with chronic renal failure with and without diabetes mellitusK Nishi, M Yoshida, Y Wada, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|August 1, 1992
[Clinical studies on pediatric purulent meningitis--clinical symptoms and prognosis]K Fukunaga, C Nishimura, H Tamaki, et al.
Journal of Endocrinological Investigation|February 7, 2013
Primary aldosteronism associated with subclinical Cushing syndromeK Fujimoto, S Honjo, H Tatsuoka, et al.
Physical Review Letters|September 7, 2019
Downward Terrestrial Gamma-Ray Flash Observed in a Winter ThunderstormY Wada, T Enoto, K Nakazawa, et al.
[Zasshi] [Journal]. Nihon Kyobu Geka Gakkai|July 1, 1989
[Postoperative thromboembolism of acquired mitral valve disease--comparison between valve replacement and commissurotomy]S Toda, K Oga, S Niu, et al.
Journal of Cardiology|January 1, 1991
[Left ventricular hypertrophy secondary to systemic hypertension: its effect on coronary hemodynamics]S Tadaoka, Y Wada, A Kimura, et al.
Clinical Genetics|May 3, 2014
Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylationH Kodera, N Ando, I Yuasa, et al.
Pageof 99

Showing results (811-820 of 982) with videos related to

Sort By:
Pageof 99
Journal of Neurology|July 1, 1988
Peripheral neuropathy with predominantly motor manifestations in a patient with carcinoma of the uterusM Yamada, S Shintani, K Mitani, et al.
Biochemical and Biophysical Research Communications|April 30, 1991
Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's diseaseT Ozawa, M Tanaka, H Ino, et al.
Biochemical and Biophysical Research Communications|January 31, 1991
Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)M Tanaka, H Ino, K Ohno, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1994
Vascular response to vasoactive agents in dialysed patients with chronic renal failure with and without diabetes mellitusK Nishi, M Yoshida, Y Wada, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|August 1, 1992
[Clinical studies on pediatric purulent meningitis--clinical symptoms and prognosis]K Fukunaga, C Nishimura, H Tamaki, et al.
Journal of Endocrinological Investigation|February 7, 2013
Primary aldosteronism associated with subclinical Cushing syndromeK Fujimoto, S Honjo, H Tatsuoka, et al.
Physical Review Letters|September 7, 2019
Downward Terrestrial Gamma-Ray Flash Observed in a Winter ThunderstormY Wada, T Enoto, K Nakazawa, et al.
[Zasshi] [Journal]. Nihon Kyobu Geka Gakkai|July 1, 1989
[Postoperative thromboembolism of acquired mitral valve disease--comparison between valve replacement and commissurotomy]S Toda, K Oga, S Niu, et al.
Journal of Cardiology|January 1, 1991
[Left ventricular hypertrophy secondary to systemic hypertension: its effect on coronary hemodynamics]S Tadaoka, Y Wada, A Kimura, et al.
Clinical Genetics|May 3, 2014
Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylationH Kodera, N Ando, I Yuasa, et al.
Pageof 99