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1681por Wang, Meng, Dehlinger, Adeline, Zapata, Camila Fernández, Golan, Maya, Gallaccio, Gerardina, Sander, Leif E., Schlickeiser, Stephan, Kunkel, Desiree, Schmitz-Hübsch, Tanja, Sawitzki, Birgit, Karni, Arnon, Braun, Julian, Loyal, Lucie, Thiel, Andreas, Bellmann-Strobl, Judith, Paul, Friedemann, Meyer-Arndt, Lil, Böttcher, Chotima“…Disease-modifying therapies (DMTs) are widely used in neuroimmunological diseases such as multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). Although these treatments are known to predispose patients to infections and affect their responses to vaccination, little is known about the impact of DMTs on the myeloid cell compartment. …”
Publicado 2023
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1682por Messias, Katharina, Moreto, Renata, Cruz, Camila Aquino, Ronchi, Nathalia Rossoni, Santos, Antonio Carlos dos, Messias, André, Marques, Vanessa Daccach“…Background Anti-myelin oligodendrocyte glycoprotein (anti-MOG) antibody-associated disease (MOGAD) is an immune-mediated neurological disorder with a broad spectrum of clinical presentation that is often difficult to distinguish from other demyelinating diseases, such as multiple sclerosis and neuromyelitis optica spectrum disorder. Objective To describe the clinical and paraclinical characteristics of MOGAD in a Brazilian tertiary center. …”
Publicado 2023
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1683“…CALI also disrupted the interaction of AQP4 with a neuromyelitis optica autoantibody directed against an extracellular epitope on AQP4. …”
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1684“…The clinical diagnosis of ON consists of the classic triad of visual loss, periocular pain and dyschromatopsia which requires careful ophthalmic, neurologic and systemic examinations to distinguish between typical and atypical ON. ON in neuromyelitis optica (NMO) is initially misdiagnosed as ON in MS or other conditions such as Anterior Ischemic Optic Neuropathy (AION) and Leber’s disease. …”
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1685por Etemadifar, Masoud, Abtahi, Mohammad-Ali, Razmjoo, Hassan, Abtahi, Seyed-Hossein, Dehghani, Ali-Reza, Abtahi, Zahra-Alsadat, Akbari, Mojtaba, Mazaheri, Shahir, Maghzi, Amir-Hadi“…BACKGROUND: Optic neuritis (ON) can be the first presentation of multiple sclerosis (MS) or neuromyelitis optica (NMO). Anti-aquaporin-4 IgG (AQP4 IgG) is a highly specific and moderately sensitive biomarker for NMO. …”
Publicado 2012
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1686Idiopathic acute transverse myelitis: outcome and conversion to multiple sclerosis in a large seriespor Cobo Calvo, Álvaro, Mañé Martínez, M Alba, Alentorn-Palau, Agustí, Bruna Escuer, Jordi, Romero Pinel, Lucía, Martínez-Yélamos, Sergio“…Two patients with positive neuromyelitis optica IgG serum antibodies were excluded. Epidemiological, clinical, laboratory, magnetic resonance imaging (MRI) data and outcome of 85 patients were analyzed. …”
Publicado 2013
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1687por Robinson, Christopher A, Adiele, Reginald C, Tham, Mylyne, Lucchinetti, Claudia F, Popescu, Bogdan FGh“…This is the first study that highlights the early and widespread astrocytic injury in the absence of demyelination in AHL, suggesting that, similarly to neuromyelitis optica and central pontine myelinolysis, demyelination in AHL is secondary to astrocyte injury.…”
Publicado 2014
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1688“…The results showed that the retinal vascular system of mice develops from the optic disc after birth, and radiates out gradually to cover the entire retina, taking the papilla optica as the center. First, the superficial vasculature is formed on the inner retinal layer; then, the vasculature extends into the inner and outer edges of the retinal inner nuclear layer, forming the deep vasculature that is parallel to the superficial vasculature. …”
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1689“…The etiologic distribution is as follows: Isolated optic neuritis- 12 (19%), multiple sclerosis- 4 (6.3%), neuromyelitis optica- 5 (7.9%), tubercular meningitis- 15 (23.8%), non-arteritic ischemic optic neuropathy, ischemic optic neuropathy complicating cavernous sinus thrombosis, cryptococcal meningitis, malignant infiltration of optic nerve, Crouzon's syndrome, calvarial thickening and traumatic occipital gliosis- 1 (1.6%) case each, idiopathic intracranial hypertension, pituitary adenoma, acute disseminated encephalomyelitis, posterior reversible leukoencephalopathy- 3 (4.8%) cases each, cortical venous thrombosis 5 (7.9%), subacute scleroing panencephalitis- 4 (6.3%) cases. …”
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1690“…RESULTS: One hundred ten of 192 patients (57%) eventually developed recurrent symptoms: 69 (63%) neuromyelitis optica (NMO) or NMO spectrum disorder, 34 (31%) non-NMO recurrent TM, and 7 (6%) systemic autoimmune disease. …”
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1691por Gelfand, Jeffrey M., Cotter, Jennifer, Klingman, Jeffrey, Huang, Eric J., Cree, Bruce A.C.“…OBJECTIVES: To describe the clinical course and neuropathology at autopsy of a patient with neuromyelitis optica (NMO) treated with alemtuzumab. METHODS: Case report. …”
Publicado 2014
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1692por Khorooshi, Reza, Asgari, Nasrin, Mørch, Marlene Thorsen, Berg, Carsten Tue, Owens, Trevor“…Serum-derived autoantibodies with predominant specificity for the astrocyte water channel aquaporin-4 (AQP4) are implicated as inducers of pathology in neuromyelitis optica (NMO), a central nervous system (CNS) demyelinating disease where activated neutrophils infiltrate, unlike in MS. …”
Publicado 2015
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1693por Gulati, Sheffali, Chakrabarty, Biswaroop, Kumar, Atin, Jain, Puneet, Patel, Harsh, Saini, Lokesh“…Amongst the 11 patients with recurrent demyelination, majority were multiple sclerosis (8/11, 72.7%) followed by neuromyelitis optica (NMO; 2/11), and multiphasic ADEM (1/11). The median disease duration and follow-up since onset for those with recurrent episodes is 4 years (2.5-4.5 years). …”
Publicado 2015
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1694por Higuchi, Osamu, Nakane, Shunya, Sakai, Waka, Maeda, Yasuhiro, Niino, Masaaki, Takahashi, Toshiyuki, Fukazawa, Toshiyuki, Kikuchi, Seiji, Fujihara, Kazuo, Matsuo, Hidenori“…OBJECTIVES: To examine anti-KIR4.1 antibodies by 2 different assays in Japanese patients with multiple sclerosis (MS) or neuromyelitis optica (NMO). METHODS: One hundred sixty serum samples from 57 patients with MS, 40 patients with NMO/NMO spectrum disorder (NMOSD), and 50 healthy controls (all were Japanese) were tested with ELISA using a synthetic peptide of the first extracellular portion of human KIR4.1. …”
Publicado 2016
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1695por Wang, Yanbing, Yan, Hong, Ding, Qixing, Mao, Cunhua, Shen, Yelong, Wang, Guangbin“…Neuromyelitis optica (NMO) is an acute or subacute lesion of demyelinating disease involving the optic nerve and spinal cord, and imaging techniques and their effects have been the focus of investigations. …”
Publicado 2016
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1696por Park, Soo Jin, Jeong, In Hye, Kong, Byung Soo, Lee, Jung-Eun, Kim, Kyoung Heon, Lee, Do Yup, Kim, Ho Jin“…These disorders include multiple sclerosis (MS), neuromyelitis optica spectrum disorder (NMOSD), and idiopathic transverse myelitis (ITM). …”
Publicado 2016
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1697por Nakamura, Yoshitsugu, Nakajima, Hideto, Tani, Hiroki, Hosokawa, Takafumi, Ishida, Shimon, Kimura, Fumiharu, Kaneko, Kimihiko, Takahashi, Toshiyuki, Nakashima, Ichiro“…BACKGROUND: Anti-Myelin oligodendrocyte glycoprotein (MOG) antibodies are detected in various demyelinating diseases, such as pediatric acute disseminated encephalomyelitis (ADEM), recurrent optic neuritis, and aquaporin-4 antibody-seronegative neuromyelitis optica spectrum disorder. We present a patient who developed anti-MOG antibody-positive ADEM following infectious mononucleosis (IM) due to Epstein–Barr virus (EBV) infection. …”
Publicado 2017
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1698por Khadse, Rutika, Ravindran, Meenakshi, Pawar, Neelam, Maharajan, Padmavathy, Rengappa, Ramakrishnan“…Four (10%) cases were diagnosed as multiple sclerosis (MS), one with neuromyelitis optica, and one with acute disseminated encephalomyelitis. …”
Publicado 2017
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1699por Çaldır, Mehmet Vedat, Çelik, Güner Koyuncu, Çiftçi, Özgür, Müderrisoğlu, İbrahim Haldun“…METHODS: In this prospective study, we included 35 patients (20 females and 15 males; mean age, 32.8±9.3 years) who were not treated with steroids and who were previously diagnosed with multiple sclerosis or neuromyelitis optica. Patients were evaluated before, 1 week after, and 3 months after the steroid treatment. …”
Publicado 2017
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1700“…In central nervous system (CNS) demyelinating disorders, such as multiple sclerosis (MS), neuromyelitis optica (NMO) and related NMO-spectrum disorders (NMO-SD), a pathogenic role for antibodies is primarily projected into enhancing ongoing CNS inflammation by directly binding to target antigens within the CNS. …”
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