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Acta Neurochirurgica|November 14, 2018
Hereditary clear cell meningiomas in a single family: three-cases reportTakuro Inoue, Satoshi Shitara, Michio Ozeki, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|May 21, 2008
Anaphylactoid transfusion reactions associated with a positively charged white-cell reduction filter: a case reportMichinori Funato, Hideo Kaneko, Michio Ozeki, et al.
Pediatric Blood & Cancer|January 26, 2016
Clinical Features and Prognosis of Generalized Lymphatic Anomaly, Kaposiform Lymphangiomatosis, and Gorham-Stout DiseaseMichio Ozeki, Akihiro Fujino, Kentaro Matsuoka, et al.
Internal Medicine (Tokyo, Japan)|February 26, 2019
Fatal Progression of Gorham-Stout Disease with Skull Base Osteomyelitis and Lateral Medullary SyndromeAkifumi Nozawa, Michio Ozeki, Tomohiro Hori, et al.
Pediatric Blood & Cancer|June 18, 2019
Potential biomarkers of kaposiform lymphangiomatosisMichio Ozeki, Akifumi Nozawa, Norio Kawamoto, et al.
Human Mutation|July 4, 2019
Mutation update on ACAT1 variants associated with mitochondrial acetoacetyl-CoA thiolase (T2) deficiencyElsayed Abdelkreem, Rajesh K Harijan, Seiji Yamaguchi, et al.
The Tohoku Journal of Experimental Medicine|April 23, 2010
High regression rate of coronary aneurysms developed in patients with immune globulin-resistant Kawasaki disease treated with steroid pulse therapyShinya Adachi, Heima Sakaguchi, Takashi Kuwahara, et al.
Experimental and Therapeutic Medicine|September 21, 2012
Relationship between the benefits of suplatast tosilate, a Th2 cytokine inhibitor, and gene polymorphisms in children with bronchial asthmaEiko Matsui, Shinji Shinoda, Osamu Fukutomi, et al.
Diagnostics (Basel, Switzerland)|January 23, 2020
Assessment of Activity of Daily Life in Mucopolysaccharidosis Type II Patients with Hematopoietic Stem Cell TransplantationYasuyuki Suzuki, Madeleine Taylor, Kenji Orii, et al.
Molecular Genetics and Metabolism|August 12, 2008
Study of deep intronic sequence exonization in a Japanese neonate with a mitochondrial trifunctional protein deficiencyJamiyan Purevsuren, Toshiyuki Fukao, Yuki Hasegawa, et al.
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