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Seiji Fukuda

Showing results (31-40 of 82) with videos related to

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The Journal of Pediatrics|April 10, 2016
Clinical Features of Carnitine Deficiency Secondary to Pivalate-Conjugated Antibiotic TherapyHironori Kobayashi, Seiji Fukuda, Kenji Yamada, et al.
Brain & Development|April 16, 2019
Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case reportKenji Yamada, Michinori Ito, Hironori Kobayashi, et al.
Brain & Development|July 11, 2009
Effect of heat stress and bezafibrate on mitochondrial beta-oxidation: comparison between cultured cells from normal and mitochondrial fatty acid oxidation disorder children using in vitro probe acylcarnitine profiling assayHong Li, Seiji Fukuda, Yuki Hasegawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 29, 2015
Metabolic disease in 10 patients with sudden unexpected death in infancy or acute life-threatening eventsTomoo Takahashi, Kenji Yamada, Hironori Kobayashi, et al.
Molecular Genetics and Metabolism|February 22, 2008
Clinical and molecular investigations of Japanese cases of glutaric acidemia type 2Yuka Yotsumoto, Yuki Hasegawa, Seiji Fukuda, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|March 9, 2010
Heat stress deteriorates mitochondrial beta-oxidation of long-chain fatty acids in cultured fibroblasts with fatty acid beta-oxidation disordersHong Li, Seiji Fukuda, Yuki Hasegawa, et al.
Molecular Genetics and Metabolism Reports|March 26, 2016
A fetus with mitochondrial trifunctional protein deficiency: Elevation of 3-OH-acylcarnitines in amniotic fluid functionally assured the genetic diagnosisRyosuke Bo, Yuki Hasegawa, Kenji Yamada, et al.
Pediatric Reports|October 27, 2015
Acute Myositis Associated with Concurrent Infection of Rotavirus and Norovirus in a 2-Year-Old GirlKei Yamamoto, Seiji Fukuda, Yuichi Mushimoto, et al.
Journal of Pediatric Urology|August 30, 2008
Idiopathic testicular infarction in a boy initially suspected to have acute epididymo-orchitis associated with mycoplasma infection and Henoch-Schönlein purpuraSeiji Fukuda, Tomoo Takahashi, Koji Kumori, et al.
Molecular Genetics and Metabolism Reports|December 18, 2019
Serum C14:1/C12:1 ratio is a useful marker for differentiating affected patients with very long-chain acyl-CoA dehydrogenase deficiency from heterozygous carriersKenji Yamada, Yoshimitsu Osawa, Hironori Kobayashi, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

Sort By:
Pageof 9
The Journal of Pediatrics|April 10, 2016
Clinical Features of Carnitine Deficiency Secondary to Pivalate-Conjugated Antibiotic TherapyHironori Kobayashi, Seiji Fukuda, Kenji Yamada, et al.
Brain & Development|April 16, 2019
Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case reportKenji Yamada, Michinori Ito, Hironori Kobayashi, et al.
Brain & Development|July 11, 2009
Effect of heat stress and bezafibrate on mitochondrial beta-oxidation: comparison between cultured cells from normal and mitochondrial fatty acid oxidation disorder children using in vitro probe acylcarnitine profiling assayHong Li, Seiji Fukuda, Yuki Hasegawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 29, 2015
Metabolic disease in 10 patients with sudden unexpected death in infancy or acute life-threatening eventsTomoo Takahashi, Kenji Yamada, Hironori Kobayashi, et al.
Molecular Genetics and Metabolism|February 22, 2008
Clinical and molecular investigations of Japanese cases of glutaric acidemia type 2Yuka Yotsumoto, Yuki Hasegawa, Seiji Fukuda, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|March 9, 2010
Heat stress deteriorates mitochondrial beta-oxidation of long-chain fatty acids in cultured fibroblasts with fatty acid beta-oxidation disordersHong Li, Seiji Fukuda, Yuki Hasegawa, et al.
Molecular Genetics and Metabolism Reports|March 26, 2016
A fetus with mitochondrial trifunctional protein deficiency: Elevation of 3-OH-acylcarnitines in amniotic fluid functionally assured the genetic diagnosisRyosuke Bo, Yuki Hasegawa, Kenji Yamada, et al.
Pediatric Reports|October 27, 2015
Acute Myositis Associated with Concurrent Infection of Rotavirus and Norovirus in a 2-Year-Old GirlKei Yamamoto, Seiji Fukuda, Yuichi Mushimoto, et al.
Journal of Pediatric Urology|August 30, 2008
Idiopathic testicular infarction in a boy initially suspected to have acute epididymo-orchitis associated with mycoplasma infection and Henoch-Schönlein purpuraSeiji Fukuda, Tomoo Takahashi, Koji Kumori, et al.
Molecular Genetics and Metabolism Reports|December 18, 2019
Serum C14:1/C12:1 ratio is a useful marker for differentiating affected patients with very long-chain acyl-CoA dehydrogenase deficiency from heterozygous carriersKenji Yamada, Yoshimitsu Osawa, Hironori Kobayashi, et al.
Pageof 9