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Michinori Ito

Showing results (1-10 of 17) with videos related to

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Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Complex I deficiency due to NDUFS8 gene mutation]Michinori Ito
Ryoikibetsu Shokogun Shirizu|December 18, 2002
[Epilepsy due to inborn errors of metabolism]Michinori Ito
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Mitochondrial pyruvate carboxylase]Michinori Ito
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Complex II deficiency due to Fp gene mutation]Michinori Ito
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Mitochondrial Pyruvate dehydrogenase]Michinori Ito
Advances in Experimental Medicine and Biology|July 30, 2017
Tyrosinemia Type I in Japan: A Report of Five CasesKimitoshi Nakamura, Michinori Ito, Yosuke Shigematsu, et al.
Journal of the Neurological Sciences|August 7, 2002
Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiencyEtsuo Naito, Michinori Ito, Ichiro Yokota, et al.
No to Hattatsu = Brain and Development|July 27, 2004
[Case of methylmalonic acidemia presenting clinically Leigh encephalopathy]Hiromichi Ito, Kenji Mori, Michinori Ito, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 18, 2004
Presumed hypoplastic intrahepatic portal system due to patent ductus venosus: Importance of direct occlusion test of ductus venosus under open laparotomyYuka Takehara, Kazuhiro Mori, Takuji Edagawa, 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.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Complex I deficiency due to NDUFS8 gene mutation]Michinori Ito
Ryoikibetsu Shokogun Shirizu|December 18, 2002
[Epilepsy due to inborn errors of metabolism]Michinori Ito
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Mitochondrial pyruvate carboxylase]Michinori Ito
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Complex II deficiency due to Fp gene mutation]Michinori Ito
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 17, 2002
[Mitochondrial Pyruvate dehydrogenase]Michinori Ito
Advances in Experimental Medicine and Biology|July 30, 2017
Tyrosinemia Type I in Japan: A Report of Five CasesKimitoshi Nakamura, Michinori Ito, Yosuke Shigematsu, et al.
Journal of the Neurological Sciences|August 7, 2002
Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiencyEtsuo Naito, Michinori Ito, Ichiro Yokota, et al.
No to Hattatsu = Brain and Development|July 27, 2004
[Case of methylmalonic acidemia presenting clinically Leigh encephalopathy]Hiromichi Ito, Kenji Mori, Michinori Ito, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 18, 2004
Presumed hypoplastic intrahepatic portal system due to patent ductus venosus: Importance of direct occlusion test of ductus venosus under open laparotomyYuka Takehara, Kazuhiro Mori, Takuji Edagawa, 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.
Pageof 2