Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
International Journal of Neonatal Screening|July 2, 2021
Current Perspectives on Neonatal Screening for Propionic Acidemia in Japan: An Unexpectedly High Incidence of Patients with Mild Disease Caused by a Common <i>PCCB</i> VariantGo Tajima, Reiko Kagawa, Fumiaki Sakura, et al.
Molecular Cancer Therapeutics|July 16, 2005
Synergistic enhancement of TRAIL- and tumor necrosis factor alpha-induced cell death by a phenoxazine derivativeKeiichi Hara, Mayumi Okamoto, Toshihiko Aki, et al.
International Journal of Neonatal Screening|February 23, 2024
Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in JapanGo Tajima, Junko Aisaki, Keiichi Hara, et al.
International Journal of Hematology|May 31, 2003
Expression of apoptosis-associated protein RCAS1 in macrophages of histiocytic necrotizing lymphadenitisYasunobu Abe, Koichi Ohshima, Manabu Nakashima, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 6, 2013
Management of advanced-stage neuroblastoma in a patient with 21-hydroxalase deficiencyAkari N Utsunomiya, Satoshi Okada, Keiichi Hara, et al.
Frontiers in Genetics|January 12, 2018
Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in <i>KMT2D</i>, a Gene Associated with Kabuki Syndrome: A Case ReportSonoko Sakata, Satoshi Okada, Kohei Aoyama, et al.
Internal Medicine (Tokyo, Japan)|October 21, 2021
A 36-year-old Man with Repeated Short-term Transient Hyperammonemia and Impaired Consciousness with a Confirmed Carbamoyl Phosphate Synthase 1 Gene Monoallelic MutationRuoyi Ishikawa, Takamichi Sugimoto, Takafumi Abe, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|April 3, 2002
[Vitamin K2 therapy for myelodysplastic syndrome]Yasunobu Abe, Koichiro Muta, Nobuhisa Hirase, et al.
Molecular Genetics and Metabolism Reports|May 23, 2017
A surviving 24-month-old patient with neonatal-onset carnitine palmitoyltransferase II deficiencyNaohiro Ikeda, Shinsuke Maruyama, Kanna Nakano, et al.
Human Genetics|April 9, 2010
Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiencyKenichiro Shirao, Satoshi Okada, Go Tajima, et al.
Pageof 3