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Kimiyoshi Ichida

Showing results (1-10 of 154) with videos related to

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Nihon Rinsho. Japanese Journal of Clinical Medicine|May 7, 2014
[Recent progress and prospects for research on urate efflux transporter ABCG2]Kimiyoshi Ichida
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan|June 2, 2024
[Uric Acid Metabolism, Uric Acid Transporters and Dysuricemia]Kimiyoshi Ichida
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Primary underproductive hypouricemia]Kimiyoshi Ichida
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Hereditary xanthinuria and molybdenum cofactor deficiency]Kimiyoshi Ichida
Nihon Jinzo Gakkai Shi|April 27, 2011
[Hereditary hypouricemia]Kimiyoshi Ichida
Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica|December 9, 2010
[Hyperuricemia and metabolic syndrome]Kimiyoshi Ichida
Nihon Rinsho. Japanese Journal of Clinical Medicine|April 16, 2008
[New antihyperuricemic medicine: febuxostat, Puricase, etc]Kimiyoshi Ichida
Genome Medicine|January 22, 2010
What lies behind serum urate concentration? Insights from genetic and genomic studiesKimiyoshi Ichida
Drug Metabolism and Pharmacokinetics|February 3, 2019
A letter of reply to the commentary by Dr. Stamp et alKimiyoshi Ichida
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 6, 2016
A novel compound heterozygous mutation in the SLC22A12 (URAT1) gene in a Japanese patient associated with renal hypouricemiaKyoko Fujita, Kimiyoshi Ichida
Pageof 16

Showing results (1-10 of 154) with videos related to

Sort By:
Pageof 16
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 7, 2014
[Recent progress and prospects for research on urate efflux transporter ABCG2]Kimiyoshi Ichida
Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan|June 2, 2024
[Uric Acid Metabolism, Uric Acid Transporters and Dysuricemia]Kimiyoshi Ichida
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Primary underproductive hypouricemia]Kimiyoshi Ichida
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Hereditary xanthinuria and molybdenum cofactor deficiency]Kimiyoshi Ichida
Nihon Jinzo Gakkai Shi|April 27, 2011
[Hereditary hypouricemia]Kimiyoshi Ichida
Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica|December 9, 2010
[Hyperuricemia and metabolic syndrome]Kimiyoshi Ichida
Nihon Rinsho. Japanese Journal of Clinical Medicine|April 16, 2008
[New antihyperuricemic medicine: febuxostat, Puricase, etc]Kimiyoshi Ichida
Genome Medicine|January 22, 2010
What lies behind serum urate concentration? Insights from genetic and genomic studiesKimiyoshi Ichida
Drug Metabolism and Pharmacokinetics|February 3, 2019
A letter of reply to the commentary by Dr. Stamp et alKimiyoshi Ichida
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 6, 2016
A novel compound heterozygous mutation in the SLC22A12 (URAT1) gene in a Japanese patient associated with renal hypouricemiaKyoko Fujita, Kimiyoshi Ichida
Pageof 16