Results 31 to 40 of about 9,281 (210)

Comparison of clinical and radiological features of Aquaporin4 (AQP-4) antibody positive Neuromyelitis Optica Spectrum Disorder (NMOSD) and Anti Myelin Oligodendrocyte Glycoprotein (Anti-MOG) syndrome-our experience from Northwest India

Annals of Indian Academy of Neurology, 2022
Background: More and more cases of myelin oligodendrocyte glycoprotein (MOG) antibody are being diagnosed with the availability of laboratory tests helping us to know the differing patterns from AQP-4 antibody disease and we need to understand the ...
Rajendra Singh Jain, Deepak Jain, Sourabh Murarka, Arvind Vyas, Bhawna Sharma, Trilochan Srivastava, Kamlesh Kumar, Yavnika Jain, Kavya Rao, Jitesh Agrawal, Shankar Tejwani   +10 more
doaj   +1 more source

Microstructural visual system changes in AQP4-antibody–seropositive NMOSD [PDF]

, 2017
Objective:To trace microstructural changes in patients with aquaporin-4 antibody (AQP4-ab)-seropositive neuromyelitis optica spectrum disorders (NMOSDs) by investigating the afferent visual system in patients without clinically overt visual symptoms or ...
Alexander Klistorner, Schmidt, F., Paul, F., Klemens Ruprecht, Bellmann-Strobl, J., Ruprecht, K., Benjamin Knier, Kuchling, J., Felix Schmidt, Chien, C., Michael Scheel, Knier, B., Klistorner, A., Claudia Chien, Zimmermann, H., Friedemann Paul, Alexander U. Brandt, Hanna Zimmermann, Thomas Korn, Oertel, F.C., Korn, T., Brandt, A.U., Frederike C. Oertel, Joseph Kuchling, Judith Bellmann-Strobl, Scheel, M.   +25 more
core   +1 more source

Neuromyelitis optica spectrum disorders with and without connective tissue disorders

BMC Neurology, 2018
Background Neuromyelitis optica spectrum disorders (NMOSD) often coexist with connective tissue disorders (CTD). The aim of this study was to investigate and compare the features of NMOSD with and without CTD.
Chun-Sheng Yang, Qiu Xia Zhang, Sheng Hui Chang, Lin Jie Zhang, Li Min Li, Yuan Qi, Jing Wang, Zhi Hua Sun, Nannan Zhangning, Li Yang, Fu-Dong Shi   +10 more
doaj   +1 more source

Higher longitudinal brain white matter atrophy rate in aquaporin-4 IgG-positive NMOSD compared with healthy controls

Scientific Reports, 2023
We aimed to compare longitudinal brain atrophy in patients with neuromyelitis optica spectrum disorder (NMOSD) with healthy controls (HCs). The atrophy rate in patients with anti-aquaporin-4 antibody-positive NMOSD (AQP4 + NMOSD) was compared with age ...
Hiroki Masuda, Masahiro Mori, Shigeki Hirano, Akiyuki Uzawa, Tomohiko Uchida, Mayumi Muto, Ryohei Ohtani, Reiji Aoki, Yoshiyuki Hirano, Japanese Alzheimer’s Disease Neuroimaging Initiative (J-ADNI), Satoshi Kuwabara   +10 more
doaj   +1 more source

Therapy challenges for NMOSD in a patient with HIV

Multiple Sclerosis Journal, 2023
Neuromyelitis optica spectrum disorder (NMOSD) in people living with HIV (PLWH) is rare and its management can be difficult. Here we report a case of an HIV patient with bilateral vision loss, who was diagnosed with AQP4-IgG-positive NMOSD in 2020 during the COVID-19 pandemic.
Daniel Engels, Joachim Havla, Stefanie Förderreuther, Tania Kümpfel   +3 more
openaire   +3 more sources

Pain in AQP4-IgG-positive and MOG-IgG-positive neuromyelitis optica spectrum disorders

Multiple Sclerosis Journal - Experimental, Translational and Clinical, 2018
Background Pain is a frequent symptom in aquaporin-4-immunoglobulin-G-positive neuromyelitis optica spectrum disorders (AQP4-IgG-pos. NMOSD). Data on pain in myelin-oligodendrocyte-glycoprotein-immunoglobulin-G autoimmunity with a clinical NMOSD ...
Susanna Asseyer, Felix Schmidt, Claudia Chien, Michael Scheel, Klemens Ruprecht, Judith Bellmann-Strobl, Alexander U Brandt, Friedemann Paul   +7 more
doaj   +1 more source

Genetic factors for susceptibility to and manifestations of neuromyelitis optica

Annals of Clinical and Translational Neurology, 2020
Objective To identify genetic factors associated with susceptibility to and clinical features of neuromyelitis optica spectrum disorders (NMOSD). Methods Genome‐wide single nucleotide polymorphism (SNP) genotyping was conducted in 211 Japanese patients ...
Takuya Matsushita, Katsuhisa Masaki, Noriko Isobe, Shinya Sato, Ken Yamamoto, Yuri Nakamura, Mitsuru Watanabe, Toshihiko Suenaga, Jun‐ichi Kira, the Japan Multiple Sclerosis Genetic Consortium   +9 more
doaj   +1 more source

AQP4 antibody assay sensitivity comparison in the era of the 2015 diagnostic criteria for NMOSD [PDF]

, 2019
We have compared five different assays for antibodies to aquaporin-4 in 181 cases of suspected Neuromyelitis optica spectrum disorders (NMOSD) and 253 controls to assess their relative utility.
Ramanathan, S, Bukhari, W, Brilot, Fabienne, Bundell, CS, Woodhall, Mark, Parratt, JDE, Waters, Patrick, Prain, K, Broadley, SA, Barnett, Michael H, Silvestrini, Roger A, Silvestrini, RA, Bukhari, Wajih, Prain, Kerri, Broadley, Simon A, Vincent, Angela, Parratt, John DE, Vincent, A, Brilot, F, Bundell, Christine S, Ramanathan, Sudarshini, Woodhall, M, Barnett, MH, Australian and New Zealand NMO Collaboration   +23 more
core   +1 more source

NMOSD—Diagnostic Dilemmas Leading towards Final Diagnosis

, 2022
(1) Background: The emergence of white matter lesions in the central nervous system (CNS) can lead to diagnostic dilemmas. They are a common radiological symptom and their patterns may overlap CNS or systemic diseases and provoke underdiagnosis or ...
Woś, Michał, Konrad Rejdak, Szewczyk, Anna K., Michał Woś, Rejdak, Konrad, Krystyna Mitosek-Szewczyk, Anna K. Szewczyk, Ewa Papuć, Mitosek-Szewczyk, Krystyna, Papuć, Ewa   +9 more
core   +1 more source

Research Progress on the Animal Models of Neuromyelitis Optica Spectrum Disorders-related Neuropathic Pain

Xiehe Yixue Zazhi, 2023
Neuromyelitis optica spectrum disorders(NMOSD), an inflammatory demyelinating disease of central nervous system, is characterized by optic neuritis, longitudinally extensive transverse myelitis, and neuropathic pain.
SONG Shujia, PEI Lijian, XU Yan, ZHANG Xue, HUANG Yuguang   +4 more
doaj   +1 more source