Search Results - "Ohga, S."
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ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia
Published in Haematologica (Roma) (01-05-2016)“…Phosphatidylserine is localized exclusively to the inner leaflet of the membrane lipid bilayer of most cells, including erythrocytes. This asymmetric…”
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Dynamics of immunocyte activation during intravenous immunoglobulin treatment in Kawasaki disease
Published in Scandinavian journal of rheumatology (02-11-2019)“…Objectives: Kawasaki disease (KD) is a systemic vasculitis of early childhood. Intravenous immunoglobulin (IVIG) is the standard treatment for KD. However,…”
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First-line treatment for severe aplastic anemia in children: bone marrow transplantation from a matched family donor versus immunosuppressive therapy
Published in Haematologica (Roma) (01-12-2014)“…The current treatment approach for severe aplastic anemia in children is based on studies performed in the 1980s, and updated evidence is required. We…”
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The Results of Radiotherapy for Primary Ocular Adnexal Malt Lymphoma
Published in International journal of radiation oncology, biology, physics (2009)Get full text
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Predictive Value of Pain Sensitization Associated with Response to Exercise Therapy in Patients with Knee Osteoarthritis: A Prospective Cohort Study
Published in Journal of pain research (30-11-2022)“…Purpose: Knee osteoarthritis (KOA) is a degenerative disease with inflammation, becoming persistent as it progresses, resulting in reduced quality of life…”
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The Japanese Immune Tolerance Induction (J‐ITI) study in haemophilia patients with inhibitor: Outcomes and successful predictors of ITI treatment
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2018)“…Introduction Immune tolerance induction (ITI) was the primary therapeutic approach to eradicate inhibitors in haemophilia patients. Several large ITI…”
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Paroxysmal nocturnal hemoglobinuria and telomere length predicts response to immunosuppressive therapy in pediatric aplastic anemia
Published in Haematologica (Roma) (01-12-2015)“…Acquired aplastic anemia is an immune-mediated disease characterized by severe defects in stem cell number resulting in hypocellular marrow and peripheral…”
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Submerged culture conditions for mycelial yield and polysaccharides production by Lyophyllum decastes
Published in Food chemistry (2007)“…The effects of various carbon and nitrogen sources, their concentrations, initial pH and fermentation duration on the production of mycelia in terms of dry…”
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Effects of Exercise-Induced Hypoalgesia at Different Aerobic Exercise Intensities in Healthy Young Adults
Published in Journal of pain research (30-11-2022)“…Purpose: Exercise-induced hypoalgesia (EIH) is a reduction in pain sensitivity that occurs following a single bout of exercise. However, little research has…”
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Post-Stroke Complex Regional Pain Syndrome and Upper Limb Inactivity in Hemiplegic Patients: A Cross-Sectional Study
Published in Journal of pain research (31-10-2022)“…Purpose: The purpose of this study was to investigate the prevalence of post-stroke complex regional pain syndrome (CRPS) and to examine the characteristics of…”
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Calcineurin inhibitors exacerbate coronary arteritis via the MyD88 signalling pathway in a murine model of Kawasaki disease
Published in Clinical and experimental immunology (01-10-2017)“…Summary Calcineurin inhibitors (CNIs) have been used off‐label for the treatment of refractory Kawasaki disease (KD). However, it remains unknown whether CNIs…”
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Peripheral blood lymphocyte telomere length as a predictor of response to immunosuppressive therapy in childhood aplastic anemia
Published in Haematologica (Roma) (01-08-2014)“…Predicting the response to immunosuppressive therapy could provide useful information to help the clinician define treatment strategies for patients with…”
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NEMO mutation as a cause of familial occurrence of Behçet's disease in female patients
Published in Clinical genetics (01-12-2010)“…Takada H, Nomura A, Ishimura M, Ichiyama M, Ohga S, Hara T. NEMO mutation as a cause of familial occurrence of Behçet's disease in female patients. Behçet's…”
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Paediatric presentation and outcome of congenital protein C deficiency in Japan
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-05-2013)“…Summary Severe heritable protein C (PC) deficiency is quite rare, although heterozygous PROC mutation is the second leading cause of genetic predisposition to…”
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Acute pericardial effusion representing the TNF-α-mediated severe inflammation but not the coronary artery outcome of Kawasaki disease
Published in Scandinavian journal of rheumatology (01-05-2015)“…Objectives: To establish the optimal inflammation control of Kawasaki disease (KD), we investigated the clinical and pathophysiological basis of pericardial…”
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