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Turkiye Klinikleri Journal of Neurology最新文献

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Açık Kalp Ameliyatı Sonrasında Alt Ekstremite Tremoru Gelişen İki Olgu
Pub Date : 1900-01-01 DOI: 10.5336/NEURO.2014-43053
Burcu Ekmekci, Sadullah Sağlam, Z. A. Tak, Ilhan Cag, Hacı Taner Bulut, M. Yılmaz
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引用次数: 0
Multipl Sklerozda Görülen Psikiyatrik Bulgular ve Bozukluklar
Pub Date : 1900-01-01 DOI: 10.5336/neuro.2016-51118
İ. Sönmez, Senem Mut, A. Bozkurt
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引用次数: 0
A Comparison of Pediatric- and Adult-Onset Multiple Sclerosis 儿童和成人多发性硬化症的比较
Pub Date : 1900-01-01 DOI: 10.5336/NEURO.2017-57919
T. Kamaşak, A. Cansu, E. Arslan, S. Şahin, Betül Diler Durgut, Beril Dilber, Tuğba Kurt, M. Terzi, C. Boz
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引用次数: 1
Alüminyum Toksisitesi ve Nörodejeneratif Hastalıklardaki Rolü
Pub Date : 1900-01-01 DOI: 10.5336/neuro.2014-41039
Hande Sipahi, Şaziye Sezin Palabiyik, S. Balci, Gönül Şahi̇n
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引用次数: 0
Kronik Rekürrens İnflamatuar Optik Nöropati
Pub Date : 1900-01-01 DOI: 10.5336/neuro.2018-59908
Caner F. Demir, İrem Taşci
{"title":"Kronik Rekürrens İnflamatuar Optik Nöropati","authors":"Caner F. Demir, İrem Taşci","doi":"10.5336/neuro.2018-59908","DOIUrl":"https://doi.org/10.5336/neuro.2018-59908","url":null,"abstract":"","PeriodicalId":322260,"journal":{"name":"Turkiye Klinikleri Journal of Neurology","volume":"38 24","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114052981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abdusens Felci ile Prezente Olan İntrakraniyal Hipotansiyon
Pub Date : 1900-01-01 DOI: 10.5336/neuro.2014-40240
A. Çoban, Tuğçe Mengi, M. Çelebisoy
A 25-years-old woman presented with headache and diplopia following spinal anesthesia. Magnetic resonance imaging (MRI) showed findings compatible with intracranial hypotension. The patient was diagnosed as having 6th cranial nerve palsy secondary to cerebrospinal fluid (CSF) leakage following dural puncture and had intravenous hydration treatment. Complete resolution of the diplopia occured 24 hours after the hydration theraphy. Orthostatic headache, low CSF opening pressure and characteristic MRI findings are essential criteria for diagnosis of intracranial hypotension. Abducens nevre palsy following spinal anesthesia is a rare and reversible complication, which is thought to be secondary to the traction of abducens nerve due to intracranial hypotension following cerebrospinal fluid leakage.
一位25岁的女性在脊髓麻醉后出现头痛和复视。磁共振成像(MRI)显示符合颅内低血压。患者经硬脑膜穿刺诊断为继发脑脊液漏的第6脑神经麻痹,经静脉水化治疗。水合治疗后24小时复视完全消退。直立性头痛、低脑脊液开口压和特征性MRI表现是诊断颅内低血压的重要标准。脊髓麻醉后外展神经麻痹是一种罕见且可逆的并发症,被认为是继发于脑脊液漏后颅内低血压引起的外展神经牵拉。
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引用次数: 0
Multipl Skleroz Seyrinde İzlenen Nadir Atak Şekilleri ve Semptomlar: Geniş Bir Multipl Sklerozlu Hasta Grubunda Retrospektif İnceleme
Pub Date : 1900-01-01 DOI: 10.5336/NEURO.2014-42494
Amber Eker, A. Tuncer, Rana Karabudak
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引用次数: 0
Relationship Between Neuroimmune Disorders and Inflammatory Bowel Diseases: Case Report 神经免疫疾病与炎症性肠病的关系:病例报告
Pub Date : 1900-01-01 DOI: 10.5336/NEURO.2015-43571
Y. Arslan, Y. Zorlu, B. Tiftikçioğlu, Irem Ilgezdi
ABS TRACT Inflammatory bowel disease (IBD) and neuroimmune disorders have a close relationship to their diseases pattern and immunologic cascade with considerable morbidity and mortality. They may have common immunological pathways related with vitamin D deficiency or hygiene hypotheses and also with T cell autoimmunity. We herein report two neuroimmune disorders with low serum vitamin D levels; multiple sclerosis and acute sensory motor axonal polyneuropathy in the course of ulcerative colitis to discuss the common immunologic mechanisms. The exact incidence of neurological IBD is unknown, with reports varying from 0.25% to 35.7%. Although a reliable differentiation may clinically not always be possible, three major pathogenic entities can be differentiated: (i) cerebrovascular disease (ii) systemic and cerebral vasculitis; (iii) immune mediated neuropathy and cerebral demyelination. IBD patients should be consulted to a neurologist and examined by neuroimaging and neurophysiological studies routinely once a year, additionally serum vitamin D levels need to be assayed and replaced in these cases.
炎症性肠病(IBD)与神经免疫疾病的发病模式和免疫级联密切相关,具有较高的发病率和死亡率。它们可能有与维生素D缺乏或卫生假说相关的共同免疫途径,也与T细胞自身免疫有关。我们在此报告两种低血清维生素D水平的神经免疫疾病;探讨溃疡性结肠炎过程中多发性硬化与急性感觉运动轴突多神经病变的共同免疫机制。神经性IBD的确切发病率尚不清楚,报道从0.25%到35.7%不等。虽然在临床上可能并不总是能够进行可靠的区分,但可以区分三种主要的致病实体:(i)脑血管病;(ii)全身和脑血管炎;(iii)免疫介导的神经病变和大脑脱髓鞘。IBD患者应咨询神经科医生,每年进行一次常规的神经影像学和神经生理学检查,此外,在这些病例中,需要检测和更换血清维生素D水平。
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引用次数: 0
The Predictive Role of CXCL12 (SDF-1 alpha) in Multiple Sclerosis CXCL12 (SDF-1 α)在多发性硬化症中的预测作用
Pub Date : 1900-01-01 DOI: 10.5336/NEURO.2018-61932
S. Mungan, N. Öztekin, I. Güzel, S. Uysal
Objective: Multiple sclerosis (MS) is an inflammatory, autoimmune, demyelinating disease characterized by multifocal inflammation, progressive myelin loss and consequent axonal demyelination. Pathogenic mechanisms of MS are oligodendrocyte damage as a result of leukocyte chemotaxis to central nervous system and production of inflammatory mediators, demyelination and neuronal injury. CXCL12 (SDF-1 alpha) is a basic chemokine which is chemoattractant for resting and activated T cells. We aimed to evaluate whether CXCL12 levels may be a predictive marker of neuroinflammation in MS patients. Material and Methods: We designed a prospective case control study of fifty-four MS patients and twenty-eight healthy controls were enrolled to the study. Plasma CXCL12 levels of the groups were measured in blood samples. The groups were compared in terms of plasma CXCL12 levels. Lymphocyte count, which is a marker of inflammation, was also compared. In the study group subsequent analysis was demonstrated the association between clinical parameters and plasma CXCL12 levels. Results: CXCL12 levels were statistically higher than the control group. Mean CXCL12 level of MS patients was 2026,5±398,7 pg/ml and the mean CXCL12 level of the controls was 1840,6±256,0 pg/ml. Lymphocyte count of the patients was also statistically higher in the study group. According to the receiver operator characteristic (ROC) curve analysis mean CXCL12 levels were discriminative factors in patients in the study group. There was no statistically significant association between plasma CXCL12 levels and clinical parameters. Conclusion: We conclude that elevations in CXCL12 levels might be a promising marker pointing out the pathogenic role of inflammation in multiple sclerosis.
目的:多发性硬化症(MS)是一种炎症性、自身免疫性、脱髓鞘疾病,其特征是多灶性炎症、进行性髓磷脂丢失和随后的轴突脱髓鞘。多发性硬化症的发病机制是由于白细胞趋化中枢神经系统和产生炎症介质导致少突胶质细胞损伤、脱髓鞘和神经元损伤。CXCL12 (SDF-1 α)是一种基本的趋化因子,是静止和活化T细胞的趋化因子。我们的目的是评估CXCL12水平是否可能是MS患者神经炎症的预测指标。材料和方法:我们设计了一项前瞻性病例对照研究,纳入54名MS患者和28名健康对照者。在血液样本中测量各组血浆CXCL12水平。比较各组血浆CXCL12水平。淋巴细胞计数,这是炎症的标志,也进行了比较。在研究组中,随后的分析证实了临床参数与血浆CXCL12水平之间的关联。结果:CXCL12水平明显高于对照组。MS患者CXCL12平均水平为2026,5±398,7 pg/ml,对照组CXCL12平均水平为1840,6±256,0 pg/ml。研究组患者淋巴细胞计数也有统计学差异。根据受试者操作特征(ROC)曲线分析,平均CXCL12水平是研究组患者的判别因素。血浆CXCL12水平与临床参数之间无统计学意义。结论:我们认为CXCL12水平的升高可能是一个有希望的标志物,指出炎症在多发性硬化症中的致病作用。
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引用次数: 0
Possible Ethylene Oxide Neuropathy: Case Report 可能的环氧乙烷神经病:1例报告
Pub Date : 1900-01-01 DOI: 10.5336/neuro.2016-54357
Y. Eren, Hayat Güven, S. Çomoğlu
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引用次数: 0
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Turkiye Klinikleri Journal of Neurology
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