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Japanese Journal of Radiology|July 21, 2016
Rebound adenoid hyperplasia after chemotherapy in pediatric patients with head and neck lymphoma: MR imaging findingsHiroki Kato, Masayuki Matsuo, Michio Ozeki, et al.
Molecular Genetics and Metabolism|August 21, 2007
Identification and characterization of a temperature-sensitive R268H mutation in the human succinyl-CoA:3-ketoacid CoA transferase (SCOT) geneToshiyuki Fukao, Petri Kursula, Elizabeth Patricia Owen, et al.
Molecular Medicine Reports|May 14, 2011
Augmented cell death with Bloom syndrome helicase deficiencyHideo Kaneko, Toshiyuki Fukao, Kimiko Kasahara, et al.
International Journal of Molecular Medicine|September 30, 2010
Mutation in the Q28SDD31SD site, but not in the two SQ sites of the survival of motor neuron protein, affects its foci formationYusuke Aoki, Toshiyuki Fukao, Gaixiu Zhang, et al.
Diagnostics (Basel, Switzerland)|February 22, 2020
Long-Term Follow-up Posthematopoietic Stem Cell Transplantation in a Japanese Patient with Type-VII MucopolysaccharidosisKenji Orii, Yasuyuki Suzuki, Shunji Tomatsu, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|November 5, 2015
[Lymphangiomatosis and Gorham-Stout disease]Michio Ozeki, Akihiro Fujino, Kentaro Matsuoka, et al.
The Tohoku Journal of Experimental Medicine|January 5, 2010
Different clinical presentation in siblings with mitochondrial acetoacetyl-CoA thiolase deficiency and identification of two novel mutationsSusanne Thümmler, Didier Dupont, Cécile Acquaviva, et al.
Molecular Medicine Reports|April 9, 2011
Comparison of mitochondrial A3243G mutation loads in easily accessible samples from a family with maternally inherited diabetes and deafnessToshiyuki Fukao, Masashi Kondo, Takahiro Yamamoto, et al.
Pediatric Blood & Cancer|December 30, 2015
Gorham-Stout Disease of the Skull Base With Hearing Loss: Dramatic Recovery and Antiangiogenic TherapyAkifumi Nozawa, Michio Ozeki, Bunya Kuze, et al.
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