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Hitoshi Osaka

Showing results (31-40 of 218) with videos related to

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Pediatric Neurology|October 8, 2013
Partial PLP1 deletion causing X-linked dominant spastic paraplegia type 2Mayumi Matsufuji, Hitoshi Osaka, Leo Gotoh, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 8, 2014
[Posterior-predominant leukoencephalopathy which was caused by methylenetetrahydrofolate reductase deficiency and successfully treated with folic acid]Asako Tamura, Ryogen Sasaki, Ken Kagawa, et al.
Pediatric Radiology|January 15, 2014
Early magnetic resonance detection of cortical necrosis and acute network injury associated with neonatal and infantile cerebral infarctionTetsuhiko Okabe, Noriko Aida, Tetsu Niwa, et al.
Molecular Genetics and Metabolism Reports|January 9, 2023
Establishment of a flow cytometry screening method for patients with glucose transporter 1 deficiency syndromeSachie Nakamura, Yasushi Ito, Hiroko Hayakawa, et al.
Viral Immunology|May 21, 2025
Viral Titer of Respiratory Syncytial Virus in the Nasal Cavity in Different Sites in Children and AdultsDaisuke Tamura, Takashi Mato, Shizuka Itoh, et al.
Neuropediatrics|December 21, 2012
A child with three episodes of reversible splenial lesionTakeshi Kouga, Mizue Iai, Sumimasa Yamashita, et al.
Molecular Genetics and Metabolism|August 26, 2015
Mutational and functional analysis of Glucose transporter I deficiency syndromeSachie Nakamura, Hitoshi Osaka, Shinichi Muramatsu, et al.
Cancer Research|November 3, 2004
Retinoic acid induces neuroblastoma cell death by inhibiting proteasomal degradation of retinoic acid receptor alphaJun-ichi Nagai, Takuya Yazawa, Koji Okudela, et al.
Viral Immunology|July 13, 2024
Clinical Evaluation of the Accuracy of the Panbio™ COVID-19/Flu A&B Rapid Panel: A Combination Antigen Rapid Diagnostic Test for the Omicron Variant and Influenza A VirusHirokazu Yamagishi, Daisuke Tamura, Masahiko Yamazaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 2, 2010
1p36 deletion syndrome associated with Prader-Willi-like phenotypeYu Tsuyusaki, Hiroshi Yoshihashi, Noritaka Furuya, et al.
Pageof 22

Showing results (31-40 of 218) with videos related to

Sort By:
Pageof 22
Pediatric Neurology|October 8, 2013
Partial PLP1 deletion causing X-linked dominant spastic paraplegia type 2Mayumi Matsufuji, Hitoshi Osaka, Leo Gotoh, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 8, 2014
[Posterior-predominant leukoencephalopathy which was caused by methylenetetrahydrofolate reductase deficiency and successfully treated with folic acid]Asako Tamura, Ryogen Sasaki, Ken Kagawa, et al.
Pediatric Radiology|January 15, 2014
Early magnetic resonance detection of cortical necrosis and acute network injury associated with neonatal and infantile cerebral infarctionTetsuhiko Okabe, Noriko Aida, Tetsu Niwa, et al.
Molecular Genetics and Metabolism Reports|January 9, 2023
Establishment of a flow cytometry screening method for patients with glucose transporter 1 deficiency syndromeSachie Nakamura, Yasushi Ito, Hiroko Hayakawa, et al.
Viral Immunology|May 21, 2025
Viral Titer of Respiratory Syncytial Virus in the Nasal Cavity in Different Sites in Children and AdultsDaisuke Tamura, Takashi Mato, Shizuka Itoh, et al.
Neuropediatrics|December 21, 2012
A child with three episodes of reversible splenial lesionTakeshi Kouga, Mizue Iai, Sumimasa Yamashita, et al.
Molecular Genetics and Metabolism|August 26, 2015
Mutational and functional analysis of Glucose transporter I deficiency syndromeSachie Nakamura, Hitoshi Osaka, Shinichi Muramatsu, et al.
Cancer Research|November 3, 2004
Retinoic acid induces neuroblastoma cell death by inhibiting proteasomal degradation of retinoic acid receptor alphaJun-ichi Nagai, Takuya Yazawa, Koji Okudela, et al.
Viral Immunology|July 13, 2024
Clinical Evaluation of the Accuracy of the Panbio™ COVID-19/Flu A&B Rapid Panel: A Combination Antigen Rapid Diagnostic Test for the Omicron Variant and Influenza A VirusHirokazu Yamagishi, Daisuke Tamura, Masahiko Yamazaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 2, 2010
1p36 deletion syndrome associated with Prader-Willi-like phenotypeYu Tsuyusaki, Hiroshi Yoshihashi, Noritaka Furuya, et al.
Pageof 22