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Neuropathology : Official Journal of the Japanese Society of Neuropathology|September 22, 2012
Contiguous ABCD1 DXS1357E deletion syndrome: report of an autopsy caseMitsuaki Iwasa, Takanori Yamagata, Masashi Mizuguchi, et al.The Journal of Pediatrics|January 30, 2002
Peroxisomal acyl CoA oxidase deficiencyYasuyuki Suzuki, Mizue Iai, Atsushi Kamei, et al.Journal of Inherited Metabolic Disease|June 22, 2016
A novel method for determining peroxisomal fatty acid β-oxidationMasashi Morita, Shun Matsumoto, Airi Okazaki, et al.Journal of Neurochemistry|June 5, 2007
Adrenoleukodystrophy: subcellular localization and degradation of adrenoleukodystrophy protein (ALDP/ABCD1) with naturally occurring missense mutationsNorimasa Takahashi, Masashi Morita, Takanori Maeda, et al.Journal of Lipid Research|April 29, 2008
Rapid UPLC-MS/MS method for routine analysis of plasma pristanic, phytanic, and very long chain fatty acid markers of peroxisomal disordersOsama Y Al-Dirbashi, Tomofumi Santa, Mohamed S Rashed, et al.American Journal of Human Genetics|July 10, 2003
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlationNaomi Matsumoto, Shigehiko Tamura, Satomi Furuki, et al.Brain & Development|January 15, 2020
POLR3A variants in striatal involvement without diffuse hypomyelinationTakuya Hiraide, Kazuo Kubota, Yu Kono, et al.Lipids|February 23, 2018
Profiling and Imaging of Phospholipids in Brains of Abcd1-Deficient MiceKotaro Hama, Yuko Fujiwara, Masashi Morita, et al.Neurogenetics|July 28, 2010
Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypesTakashi Matsukawa, Muriel Asheuer, Yuji Takahashi, et al.Brain & Development|July 19, 2005
Natural history of X-linked adrenoleukodystrophy in JapanYasuyuki Suzuki, Yasuhiko Takemoto, Nobuyuki Shimozawa, et al.Pageof 8