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Hitoshi Osaka

Showing results (121-130 of 218) with videos related to

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Brain & Development|September 17, 2017
Japanese Leigh syndrome case treated with EPI-743Takeshi Kouga, Mariko Takagi, Akihiko Miyauchi, et al.
Epilepsia|January 15, 2014
PIGO mutations in intractable epilepsy and severe developmental delay with mild elevation of alkaline phosphatase levelsKazuyuki Nakamura, Hitoshi Osaka, Yoshiko Murakami, et al.
Brain & Development|September 15, 2018
Aggregate formation analysis of GFAPJanyerkye Tulyeu, Moe Tamaura, Eriko Jimbo, et al.
Antioxidants (Basel, Switzerland)|July 27, 2024
Apomorphine Suppresses the Progression of Steatohepatitis by Inhibiting FerroptosisHiroshi Maeda, Kouichi Miura, Kenichi Aizawa, et al.
Pharmaceuticals (Basel, Switzerland)|May 4, 2026
Minimally Invasive Therapeutic Drug Monitoring of Immunosuppressants in Children with Kidney Diseases: Validation of Fingerstick Sampling Using LC-MS/MSMarika Ishii, Jun Aoyagi, Natsuka Kimura, et al.
American Journal of Human Genetics|January 3, 2012
De novo and inherited mutations in COL4A2, encoding the type IV collagen α2 chain cause porencephalyYuriko Yoneda, Kazuhiro Haginoya, Hiroshi Arai, et al.
Human Genetics|October 9, 2013
A hemizygous GYG2 mutation and Leigh syndrome: a possible link?Eri Imagawa, Hitoshi Osaka, Akio Yamashita, et al.
Journal of Inherited Metabolic Disease|January 7, 2010
A new case of GABA transaminase deficiency facilitated by proton MR spectroscopyMegumi Tsuji, Noriko Aida, Takayuki Obata, et al.
The Journal of Gene Medicine|April 7, 2018
Gene therapy for Glut1-deficient mouse using an adeno-associated virus vector with the human intrinsic GLUT1 promoterSachie Nakamura, Shin-Ichi Muramatsu, Naomi Takino, et al.
International Heart Journal|September 14, 2022
A Case of Infantile Mitochondrial Cardiomyopathy Treated with a Combination of Low-Dose Propranolol and Cibenzoline for Left Ventricular Outflow Tract StenosisHironori Shimozawa, Tomoyuki Sato, Hitoshi Osaka, et al.
Pageof 22

Showing results (121-130 of 218) with videos related to

Sort By:
Pageof 22
Brain & Development|September 17, 2017
Japanese Leigh syndrome case treated with EPI-743Takeshi Kouga, Mariko Takagi, Akihiko Miyauchi, et al.
Epilepsia|January 15, 2014
PIGO mutations in intractable epilepsy and severe developmental delay with mild elevation of alkaline phosphatase levelsKazuyuki Nakamura, Hitoshi Osaka, Yoshiko Murakami, et al.
Brain & Development|September 15, 2018
Aggregate formation analysis of GFAPJanyerkye Tulyeu, Moe Tamaura, Eriko Jimbo, et al.
Antioxidants (Basel, Switzerland)|July 27, 2024
Apomorphine Suppresses the Progression of Steatohepatitis by Inhibiting FerroptosisHiroshi Maeda, Kouichi Miura, Kenichi Aizawa, et al.
Pharmaceuticals (Basel, Switzerland)|May 4, 2026
Minimally Invasive Therapeutic Drug Monitoring of Immunosuppressants in Children with Kidney Diseases: Validation of Fingerstick Sampling Using LC-MS/MSMarika Ishii, Jun Aoyagi, Natsuka Kimura, et al.
American Journal of Human Genetics|January 3, 2012
De novo and inherited mutations in COL4A2, encoding the type IV collagen α2 chain cause porencephalyYuriko Yoneda, Kazuhiro Haginoya, Hiroshi Arai, et al.
Human Genetics|October 9, 2013
A hemizygous GYG2 mutation and Leigh syndrome: a possible link?Eri Imagawa, Hitoshi Osaka, Akio Yamashita, et al.
Journal of Inherited Metabolic Disease|January 7, 2010
A new case of GABA transaminase deficiency facilitated by proton MR spectroscopyMegumi Tsuji, Noriko Aida, Takayuki Obata, et al.
The Journal of Gene Medicine|April 7, 2018
Gene therapy for Glut1-deficient mouse using an adeno-associated virus vector with the human intrinsic GLUT1 promoterSachie Nakamura, Shin-Ichi Muramatsu, Naomi Takino, et al.
International Heart Journal|September 14, 2022
A Case of Infantile Mitochondrial Cardiomyopathy Treated with a Combination of Low-Dose Propranolol and Cibenzoline for Left Ventricular Outflow Tract StenosisHironori Shimozawa, Tomoyuki Sato, Hitoshi Osaka, et al.
Pageof 22