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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 Cases
Kimitoshi 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 deficiency
Etsuo 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 laparotomy
Yuka 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 report
Kenji Yamada, Michinori Ito, Hironori Kobayashi, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 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 Cases
Kimitoshi 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 deficiency
Etsuo 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 laparotomy
Yuka 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 report
Kenji Yamada, Michinori Ito, Hironori Kobayashi, et al.
Page
of 2