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Pediatric Hematology and Oncology|September 6, 2007
Clinical improvement of diffuse lymphangiomatosis with pegylated interferon alfa-2b therapy: case report and review of the literatureMichio Ozeki, Michinori Funato, Kaori Kanda, et al.Scientific Reports|April 18, 2019
An innate interaction between IL-18 and the propeptide that inactivates its precursor formNaotaka Tsutsumi, Ayumi Yokota, Takeshi Kimura, et al.Thrombosis Research|September 11, 2009
A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimersMichio Ozeki, Shinji Kunishima, Kimiko Kasahara, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 9, 2010
Reversible cerebrospinal fluid edema and porencephalic cyst, a rare complication of ventricular catheterMichio Ozeki, Michinori Funato, Takahide Teramoto, et al.Molecular Genetics and Metabolism|June 13, 2006
A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiencyToshiyuki Fukao, Satomi Sakurai, Marie-Odile Rolland, et al.Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|August 28, 2007
Clinical and bacteriological evaluation of the efficacy of piperacillin in children with pneumoniaMinako Aoki, Toshiyuki Fukao, Hideo Kaneko, et al.Molecular Genetics & Genomic Medicine|June 11, 2024
Loss-of-function polymorphisms in NQO1 are not associated with the development of subacute myelo-optico-neuropathyHideki Matsumoto, Hideo Sasai, Norio Kawamoto, et al.Human Genome Variation|April 8, 2020
Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiencyMina Nakama, Hideo Sasai, Mitsuru Kubota, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|September 25, 2014
Facial palsy as an unusual presenting symptom associated with acute myeloid leukemiaKazuo Kubota, Michio Ozeki, Tomohiro Hori, et al.Molecular Genetics and Metabolism|August 28, 2007
Identification of an Alu-mediated tandem duplication of exons 8 and 9 in a patient with mitochondrial acetoacetyl-CoA thiolase (T2) deficiencyToshiyuki Fukao, Gaixiu Zhang, Marie-Odile Rolland, et al.Pageof 20