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Brain & Development|April 8, 2011
Molecular and clinical findings and diagnostic flowchart of peroxisomal diseasesNobuyuki ShimozawaBrain and Nerve = Shinkei Kenkyu No Shinpo|May 12, 2025
[Neurological Peroxisomal Disorders with a Focus on Adrenoleukodystrophy]Nobuyuki ShimozawaJournal of Human Genetics|September 22, 2018
Expanding the concept of peroxisomal diseases and efficient diagnostic system in JapanShigeo Takashima, Hirotomo Saitsu, Nobuyuki ShimozawaJournal of General and Family Medicine|August 4, 2020
A case of female adrenoleukodystrophy carrier with insidious neurogenic bladderKoji Obara, Erika Abe, Nobuyuki Shimozawa, et al.Brain & Development|December 19, 2012
Newly identified milder phenotype of peroxisome biogenesis disorder caused by mutated PEX3 geneShuji Matsui, Masuko Funahashi, Ayako Honda, et al.Brain & Development|April 24, 2008
Parents of childhood X-linked adrenoleukodystrophy: high risk for depression and neurosisIzumi Kuratsubo, Yasuyuki Suzuki, Nobuyuki Shimozawa, et al.International Journal of Molecular Sciences|August 27, 2021
Glycosphingolipids with Very Long-Chain Fatty Acids Accumulate in Fibroblasts from Adrenoleukodystrophy PatientsYuko Fujiwara, Kotaro Hama, Nobuyuki Shimozawa, et al.Scientific Reports|August 2, 2020
Positional determination of the carbon-carbon double bonds in unsaturated fatty acids mediated by solvent plasmatization using LC-MSShigeo Takashima, Kayoko Toyoshi, Takuhei Yamamoto, et al.Current Drug Targets|November 3, 2010
ABC subfamily D proteins and very long chain fatty acid metabolism as novel targets in adrenoleukodystrophyM Morita, Nobuyuki Shimozawa, Yoshinori Kashiwayama, et al.Neuroscience Letters|July 10, 2008
Changes in the amounts of myelin lipids and molecular species of plasmalogen PE in the brain of an autopsy case with D-bifunctional protein deficiencyMakiko Saitoh, Sumimasa Yamashita, Nobuyuki Shimozawa, et al.Pageof 8