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F Kanda

Showing results (41-50 of 72) with videos related to

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Biochimica Et Biophysica Acta|March 7, 1986
Substrate recognition of isopeptidase: specific cleavage of the epsilon-(alpha-glycyl)lysine linkage in ubiquitin-protein conjugatesF Kanda, D E Sykes, H Yasuda, et al.
The British Journal of Dermatology|June 1, 1990
Elucidation of chemical compounds responsible for foot malodourF Kanda, E Yagi, M Fukuda, et al.
Journal of the Neurological Sciences|November 1, 1987
Neuropathological changes of the brain in myotonic dystrophy--some new observationsS Ono, K Inoue, T Mannen, et al.
Hormone Research|January 12, 2002
Steroid myopathy: pathogenesis and effects of growth hormone and insulin-like growth factor-I administrationF Kanda, S Okuda, T Matsushita, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 19, 2009
Effect of alendronate on bone metabolic indices and bone mineral density in patients treated with high-dose glucocorticoid: a prospective studyH Kaji, Y Kuroki, Y Murakawa, et al.
Hinyokika Kiyo. Acta Urologica Japonica|March 10, 2001
[A survey of radical surgery without neoadjuvant therapy for patients with stage B and C prostatic carcinoma]J Matsuzaki, F Kanda, T Watanabe, et al.
Journal of Neurology|February 1, 1990
Acute autonomic and sensory neuropathy: a case reportF Kanda, T Uchida, K Jinnai, et al.
European Neurology|January 1, 1990
A case of mitochondrial myopathy, encephalopathy and lactic acidosis due to cytochrome c oxidase deficiency with neurogenic muscular changesK Jinnai, H Yamada, F Kanda, et al.
Electromyography and Clinical Neurophysiology|July 1, 1989
Somatosensory evoked potentials in Huntington's disease--studies with paired stimulationF Kanda, K Jinnai, K Takahashi, et al.
Human Mutation|November 26, 1999
Glycogen storage disease type IIIa: first report of a causative missense mutation (G1448R) of the glycogen debranching enzyme gene found in a homozygous patientM Okubo, F Kanda, A Horinishi, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Biochimica Et Biophysica Acta|March 7, 1986
Substrate recognition of isopeptidase: specific cleavage of the epsilon-(alpha-glycyl)lysine linkage in ubiquitin-protein conjugatesF Kanda, D E Sykes, H Yasuda, et al.
The British Journal of Dermatology|June 1, 1990
Elucidation of chemical compounds responsible for foot malodourF Kanda, E Yagi, M Fukuda, et al.
Journal of the Neurological Sciences|November 1, 1987
Neuropathological changes of the brain in myotonic dystrophy--some new observationsS Ono, K Inoue, T Mannen, et al.
Hormone Research|January 12, 2002
Steroid myopathy: pathogenesis and effects of growth hormone and insulin-like growth factor-I administrationF Kanda, S Okuda, T Matsushita, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 19, 2009
Effect of alendronate on bone metabolic indices and bone mineral density in patients treated with high-dose glucocorticoid: a prospective studyH Kaji, Y Kuroki, Y Murakawa, et al.
Hinyokika Kiyo. Acta Urologica Japonica|March 10, 2001
[A survey of radical surgery without neoadjuvant therapy for patients with stage B and C prostatic carcinoma]J Matsuzaki, F Kanda, T Watanabe, et al.
Journal of Neurology|February 1, 1990
Acute autonomic and sensory neuropathy: a case reportF Kanda, T Uchida, K Jinnai, et al.
European Neurology|January 1, 1990
A case of mitochondrial myopathy, encephalopathy and lactic acidosis due to cytochrome c oxidase deficiency with neurogenic muscular changesK Jinnai, H Yamada, F Kanda, et al.
Electromyography and Clinical Neurophysiology|July 1, 1989
Somatosensory evoked potentials in Huntington's disease--studies with paired stimulationF Kanda, K Jinnai, K Takahashi, et al.
Human Mutation|November 26, 1999
Glycogen storage disease type IIIa: first report of a causative missense mutation (G1448R) of the glycogen debranching enzyme gene found in a homozygous patientM Okubo, F Kanda, A Horinishi, et al.
Pageof 8