نتایج جستجو برای: کشیدگی nmo

تعداد نتایج: 1703  

2017
Fumitaka Shimizu Richard M. Ransohoff

Antibody-based therapy offers vast potential in the treatment of several neurodegenerative diseases. Many drug companies are now engineering antibodies targeting β-amyloid protein for Alzheimer disease and α-synuclein protein for Parkinson disease. However, the development of antibody-based therapies against the central nervous system (CNS) diseases has lagged, partly due to the poor blood-brai...

Journal: :Journal of the neurological sciences 2012
Xuan Feng Nicholas P Reder Mounica Yanamandala Addie Hill Beverly S Franek Timothy B Niewold Anthony T Reder Adil Javed

OBJECTIVE Neuromyelitis optica (NMO) is characterized by selective inflammation of the spinal cord and optic nerves but is distinct from multiple sclerosis (MS). Interferon (IFN)-β mitigates disease activity in MS, but is controversial in NMO, with a few reports of disease worsening after IFN-β therapy in this highly active disease. In systemic lupus erythematosus (SLE), IFNs adversely affect d...

2014
Lukmanee Tradtrantip Nithi Asavapanumas Puay-Wah Phuan A. S. Verkman

Neuromyelitis optica (NMO) is an autoimmune demyelinating disease of the central nervous system in which binding of anti-aquaporin-4 (AQP4) autoantibodies (NMO-IgG) to astrocytes causes complement-dependent cytotoxicity (CDC) and inflammation resulting in oligodendrocyte and neuronal injury. There is compelling evidence for a central role of complement in NMO pathogenesis. Here, we evaluated th...

2011
Masoud Etemadifar Seyed-Hossein Abtahi Alireza Dehghani Mohammad-Ali Abtahi Mojtaba Akbari Nasim Tabrizi Tannaz Goodarzi

Neuromyelitis optica (NMO) is an inflammatory demyelinating disorder of the central nervous system that has been thought to be a severe subtype of multiple sclerosis for a long time. The discovery of aquaporin-4 (AQP4) antibody as a highly specific marker responsible for the pathogenesis of NMO, not only has made a revolutionary pace in establishing a serologic distinction between the two disea...

2014
Sung-Min Kim Patrick Waters Mark Woodhall Ji Won Yang Hyeran Yang Jee-Eun Kim Jung-Joon Sung Kyung Seok Park Kwang-Woo Lee

BACKGROUND The relative frequencies of demyelinating diseases among Korean patients with idiopathic inflammatory demyelinating disease of the central nervous system (IIDD) have not been sufficiently studied. We therefore describe a cohort of 203 patients with IIDD from three centers in Korea whose syndromes were identified precisely according to international clinical criteria and autoantibody ...

2015
Regina Maria Papais-Alvarenga Claudia Cristina Ferreira Vasconcelos Adriana Carra Ibis Soto de Castillo Sara Florentin Fernando Hamuy Diaz de Bedoya Raul Mandler Luiza Campanella de Siervi Maria Lúcia Vellutini Pimentel Marina Papais Alvarenga Marcos Papais Alvarenga Anderson Kuntz Grzesiuk Ana Beatriz Calmon Gama Pereira Antonio Pereira Gomes Neto Carolina Velasquez Carlos Soublette Cynthia Veronica Fleitas Denise Sisteroli Diniz Elizabeth Armas Elizabeth Batista Freda Hernandez Fernanda Ferreira Chaves da Costa Pereira Heloise Helena Siqueira Hideraldo Cabeça Jose Sanchez Joseph Bruno Bidin Brooks Marcus Vinicius Gonçalves Maria Cristina Del Negro Barroso Maria Elena Ravelo Maria Carlota Castillo Maria Lúcia Brito Ferreira Maria Sheila Guimarães Rocha Monica Koncke Fiuza Parolin Omaira Molina Patricia Beatriz Christino Marinho Paulo Pereira Christo Renata Brant de Souza Silvio Pessanha Neto Solange Maria das Graças Camargo Suzana Costa Machado Vanderson Carvalho Neri Yara Dadalti Fragoso Helcio Alvarenga Luiz Claudio Santos Thuler Markus Reindl

The idiopathic inflammatory demyelinating disease (IIDD) spectrum has been investigated among different populations, and the results have indicated a low relative frequency of neuromyelitis optica (NMO) among multiple sclerosis (MS) cases in whites (1.2%-1.5%), increasing in Mestizos (8%) and Africans (15.4%-27.5%) living in areas of low MS prevalence. South America (SA) was colonized by Europe...

Journal: :مجله علوم اعصاب شفای خاتم 0
mohammad ali sahraian neuroscience institute, tehran university of medical sciences, tehran, iran

typical nmo is characterized by simultaneous or sequential acute transverse myelitis and optic neuritis. spinal cord lesions extending over 3 or more vertebral segments and normal brain imaging are the typical mri findings in nmo. in typical cases with positive nmo antibody the diagnosis is easy but in seronegative and atypical cases with different clinical manifestations and mri features the d...

2016
Massa Zantah Timothy B. Coyle Debapriya Datta

Neuromyelitis Optica (NMO) is a demyelinating autoimmune disease involving the central nervous system. Acute respiratory failure from cervical myelitis due to NMO is known to occur but is uncommon in monophasic disease and is treated with high dose steroids. We report a case of a patient with NMO who developed acute respiratory failure related to cervical spinal cord involvement, refractory to ...

2015
Yanxia Huang Lei Zhang Yinyao Lin Yanqiang Wang Bingjun Zhang Xuejiao Men Zhengqi Lu

Results: The relapse number, Expanded Disability Status Scale (EDSS) score at initial diagnosis, and EDSS score at last visit were significantly higher in NMO patients with brain abnormalities than those in NMO patients without brain abnormalities, respectively. NMO patients with brainstem involvement had higher relapse number, EDSS score at initial diagnosis, and EDSS score at last visit than ...

2013
Katsuhisa Masaki Satoshi O. Suzuki Takuya Matsushita Takeshi Matsuoka Shihoko Imamura Ryo Yamasaki Makiko Suzuki Toshihiko Suenaga Toru Iwaki Jun-Ichi Kira

BACKGROUND Multiple sclerosis (MS) and neuromyelitis optica (NMO) occasionally have an extremely aggressive and debilitating disease course; however, its molecular basis is unknown. This study aimed to determine a relationship between connexin (Cx) pathology and disease aggressiveness in Asian patients with MS and NMO. METHODS/PRINCIPAL FINDINGS Samples included 11 autopsied cases with NMO an...

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