Immunoadsorption in neurological disorders

S Oji, K Nomura - Transfusion and apheresis science, 2017 - Elsevier
In recent years, immunoadsorption has been increasingly recognized as an alternative to
therapeutic plasma exchange and used for the treatment of neurological disorders such as …

The Japanese Society for Apheresis clinical practice guideline for therapeutic apheresis

T Abe, H Matsuo, R Abe, S Abe… - Therapeutic …, 2021 - Wiley Online Library
Most of the diseases for which apheresis therapy is indicated are intractable and rare, and
each patient has a different background and treatment course prior to apheresis therapy …

[HTML][HTML] Nationwide laboratory surveillance of progressive multifocal leukoencephalopathy in Japan: fiscal years 2011–2020

K Nakamichi, Y Miura, T Shimokawa, K Takahashi… - Viruses, 2023 - mdpi.com
Progressive multifocal leukoencephalopathy (PML) is a devastating demyelinating disease
caused by JC virus (JCV), predominantly affecting patients with impaired cellular immunity …

[HTML][HTML] Quality of life in purely ocular myasthenia in Japan

S Suzuki, H Murai, T Imai, Y Nagane, M Masuda… - BMC neurology, 2014 - Springer
Background Since there has been no conclusive evidence regarding the treatment of ocular
myasthenia, treatment guidelines were recently issued by the European Federation of …

Anti-MOG antibody–associated disorders: differences in clinical profiles and prognosis in Japan and Germany

J Liu, M Mori, H Zimmermann, A Brandt… - Journal of Neurology …, 2021 - jnnp.bmj.com
Background Neurological disorders with IgG antibodies against myelin-oligodendrocyte
glycoprotein (MOG-IgG) have been increasingly recognised as a new type of …

A clinical predictive score for postoperative myasthenic crisis

T Kanai, A Uzawa, Y Sato, S Suzuki… - Annals of …, 2017 - Wiley Online Library
Objective Myasthenia gravis (MG) is an autoimmune disease mostly caused by
autoantibodies against acetylcholine receptor associated with thymus abnormalities …

Clinical and immunological differences between MOG associated disease and anti AQP4 antibody-positive neuromyelitis optica spectrum disorders: Blood–brain …

S Tanaka, B Hashimoto, S Izaki, S Oji… - Multiple Sclerosis and …, 2020 - Elsevier
Background Patients with anti-aquaporin-4 (AQP4) water channel antibody-positive
neuromyelitis optica spectrum disorders (AQP4-NMOSD) and myelin oligodendrocyte …

Mean platelet volume is associated with early neurological deterioration in patients with branch atheromatous disease: involvement of platelet activation

S Oji, D Tomohisa, W Hara, T Tajima, M Suzuki… - Journal of Stroke and …, 2018 - Elsevier
Background The most attentive clinical problem in patients with branch atheromatous
disease (BAD) is early neurological deterioration (END). Although the platelet activation …

Real‐world application of plasmapheresis for neurological disease: Results from the Japan‐Plasmapheresis Outcome and Practice Patterns Study

Y Lin, S Oji, K Miyamoto, T Narita… - Therapeutic …, 2023 - Wiley Online Library
Introduction Plasmapheresis is a well‐recognized treatment for autoimmune neurological
diseases in Japan. However, the practice varies depending on the facility, and the actual …

The accuracy of flow cytometric cell-based assay to detect anti-myelin oligodendrocyte glycoprotein (MOG) antibodies determining the optimal method for positivity …

K Sugimoto, M Mori, J Liu, S Tanaka, K Kaneko… - Journal of …, 2019 - Elsevier
To illustrate the accuracy of the fluorescence-activated cell sorting cell-based assay (FACS-
CBA) and to detect anti-myelin oligodendrocyte glycoprotein (MOG) antibodies and …