首页 > 最新文献

Russian Neurological Journal最新文献

英文 中文
Autoimmune аnti-NMDA encephalitis associated with the new coronavirus infection COVID-19 与新型冠状病毒感染COVID-19相关的自身免疫性抗nmda脑炎
Q4 Medicine Pub Date : 2023-10-02 DOI: 10.30629/2658-7947-2023-28-4-60-67
N. I. Panchenko, N. V. Shuleshova, D. I. Rudenko, D. I. Skulyabin, S. A. Kolchev, S. V. Perfilev, S. V. Lapin
The article presents a clinical case of a 19-year-old patient with reliable autoimmune anti-NMDA encephalitis, developed after a coronavirus infection, which was accompanied by the signs of catatonia, epilepsy and mutism at the onset of the disease. This case enlarges the statistics of observations of this pathology by including the SARS-COV 2 virus to the list of possible etiological factors. The analysis of the catatonia signs, dominating at the onset of the disease, was carried out.
本文报道一名19岁的可靠自身免疫性抗nmda脑炎患者,在冠状病毒感染后发展,发病时伴有紧张症、癫痫和失语症状。该病例通过将SARS-COV - 2病毒列入可能的病因清单,扩大了该病理观察的统计数据。分析了在疾病发病时占主导地位的紧张症体征。
{"title":"Autoimmune аnti-NMDA encephalitis associated with the new coronavirus infection COVID-19","authors":"N. I. Panchenko, N. V. Shuleshova, D. I. Rudenko, D. I. Skulyabin, S. A. Kolchev, S. V. Perfilev, S. V. Lapin","doi":"10.30629/2658-7947-2023-28-4-60-67","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-4-60-67","url":null,"abstract":"The article presents a clinical case of a 19-year-old patient with reliable autoimmune anti-NMDA encephalitis, developed after a coronavirus infection, which was accompanied by the signs of catatonia, epilepsy and mutism at the onset of the disease. This case enlarges the statistics of observations of this pathology by including the SARS-COV 2 virus to the list of possible etiological factors. The analysis of the catatonia signs, dominating at the onset of the disease, was carried out.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":"102 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135899250","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
Paraneoplastic cerebellar degeneration 副肿瘤小脑变性
Q4 Medicine Pub Date : 2023-10-02 DOI: 10.30629/2658-7947-2023-28-4-43-53
E. P. Nuzhnyi, M. Yu. Krasnov, A. N. Moskalenko, E. Yu. Fedotova, E. O. Chekanova, S. N. Illarioshkin
Introduction. Paraneoplastic cerebellar degeneration (PCD) is an immune-mediated and rapidly progressive cerebellar syndrome that develops as a result of a cross-immune response to the common antigens for the tumor and cerebellar cells. Timely diagnosis and treatment of PCD improves the functional status and survival of these patients.Objective. To analyze the clinical, laboratory and neuroimaging characteristics of PCD case series in comparison with literature data.Material and methods. 16 patients with PCD (13 women, 3 men) were examined. An assessment of the clinical presentation, brain MRI study, blood and cerebrospinal fl uid laboratory tests were carried out, the data of cancer search and patients follow-up were analyzed.Results. The median age of PCD patients was 55 years, the duration of the disease was 8.5 months (range 4 to 16 months). In 12 patients, PCD was the fi rst manifestation of cancer. The clinical prentation was presented by rapidly progressive cerebellar ataxia, often in combination with oculomotor disturbances, pyramidal and bulbar syndrome, hand tremor and dystonia. An associated cancers were detected in 13 patients (81%). Antineuronal antibodies were found in 14 patients (88%): anti-Yo-1, antibodies to amphiphysin, anti-Hu, anti-CV2 and anti-GAD. Mild atrophic changes of the cerebellum were found in 6 patients, and in 2 cases cerebellar hemiatrophy was observed.Conclusion. PCD is a rare disabling but potentially curable disease. The basis of diagnosis is the analysis of the clinical presentation and neuroimaging data, the detection of antineuronal antibodies and in fl ammatory changes in the cerebrospinal fl uid, as well as a thorough cancer search.
介绍。副肿瘤小脑变性(PCD)是一种免疫介导的快速进展的小脑综合征,是由于肿瘤和小脑细胞对共同抗原的交叉免疫反应而发展起来的。及时诊断和治疗可提高PCD患者的功能状态和生存率。目的:分析PCD病例系列的临床、实验室和神经影像学特征,并与文献资料进行比较。材料和方法。本文对16例PCD患者(女13例,男3例)进行了检查。对患者的临床表现、脑MRI检查、血液和脑脊液实验室检查进行了评估,并对患者的癌症搜索和随访数据进行了分析。PCD患者的中位年龄为55岁,病程为8.5个月(4 - 16个月)。在12例患者中,PCD是癌症的第一表现。临床表现为快速进行性小脑共济失调,常合并动眼肌障碍、锥体和球体综合征、手颤和肌张力障碍。13例患者(81%)检出相关癌症。14例(88%)患者发现抗神经元抗体:抗yo -1、抗amphiphysin、抗hu、抗cv2和抗gad。6例患者出现小脑轻度萎缩改变,2例出现小脑半萎缩。PCD是一种罕见的致残但有治愈潜力的疾病。诊断的基础是分析临床表现和神经影像学资料,检测抗神经元抗体和脑脊液炎性变化,以及彻底的癌症搜索。
{"title":"Paraneoplastic cerebellar degeneration","authors":"E. P. Nuzhnyi, M. Yu. Krasnov, A. N. Moskalenko, E. Yu. Fedotova, E. O. Chekanova, S. N. Illarioshkin","doi":"10.30629/2658-7947-2023-28-4-43-53","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-4-43-53","url":null,"abstract":"Introduction. Paraneoplastic cerebellar degeneration (PCD) is an immune-mediated and rapidly progressive cerebellar syndrome that develops as a result of a cross-immune response to the common antigens for the tumor and cerebellar cells. Timely diagnosis and treatment of PCD improves the functional status and survival of these patients.Objective. To analyze the clinical, laboratory and neuroimaging characteristics of PCD case series in comparison with literature data.Material and methods. 16 patients with PCD (13 women, 3 men) were examined. An assessment of the clinical presentation, brain MRI study, blood and cerebrospinal fl uid laboratory tests were carried out, the data of cancer search and patients follow-up were analyzed.Results. The median age of PCD patients was 55 years, the duration of the disease was 8.5 months (range 4 to 16 months). In 12 patients, PCD was the fi rst manifestation of cancer. The clinical prentation was presented by rapidly progressive cerebellar ataxia, often in combination with oculomotor disturbances, pyramidal and bulbar syndrome, hand tremor and dystonia. An associated cancers were detected in 13 patients (81%). Antineuronal antibodies were found in 14 patients (88%): anti-Yo-1, antibodies to amphiphysin, anti-Hu, anti-CV2 and anti-GAD. Mild atrophic changes of the cerebellum were found in 6 patients, and in 2 cases cerebellar hemiatrophy was observed.Conclusion. PCD is a rare disabling but potentially curable disease. The basis of diagnosis is the analysis of the clinical presentation and neuroimaging data, the detection of antineuronal antibodies and in fl ammatory changes in the cerebrospinal fl uid, as well as a thorough cancer search.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135900156","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
Assessment of biomechanical parameters of feet in patients with multiple sclerosis during walking 多发性硬化症患者步行时足部生物力学参数的评估
Q4 Medicine Pub Date : 2023-10-02 DOI: 10.30629/2658-7947-2023-28-4-35-42
A. D. Dorokhov, E. V. Ivashkova, A. G. Ilves, K. K. Mineev, I. G. Negoreeva, A. M. Petrov, L. N. Prakhova, I. D. Stolyarov, G. G. Shkilnyuk, V. N. Tartakovskiy, T. L. Tcvetkova, V. A. Zubarev
Rationale. Walking and balance disorders, modi fi ed foot muscles kinematics and walking stereotypes are typical for the patients with Multiple Sclerosis (MS).Objective. To assess the biomechanical parameters of the feet in MS patients with diff erent neurological status during walking.Material and methods. Data analysis of 102 patients with relapsing-remitting MS was carried out for two groups depending on the value of the Expanded Disability Status Scale (EDSS). Plantar pressure distribution was measured on with the pedographic platform emed, novel gmbh, Munich, Germany, using a “fi rst step” protocol.Results and conclusion. Loading of the heel, the area of central metatarsal heads is decreased and loading of the toes is increased during walking in MS patients. Diff erences were found for the spreading coeffi cient (the ratio of the width to the length of the foot), the dynamic width of the foot in patients with an EDSS ≥ 4 is signi fi cantly less in the instep, in the middle and in the narrowest parts of the foot, which leads to the decrease of the contact area. It has been shown that patients with MS who are mobile or walk without assistance are more likely to have pes cavus foot compared to MS patients with minor impairments. The load of the medial side of the foot is greater than the lateral side, which indicates the predominance of the valgus foot. The pronation-supination index is signi fi cantly higher in the patients with moderate impairments in toe-off phase. Evaluation of foot deformity based on the measurement of biomechanical parameters of plantar pressure distribution makes it possible to plan the treatment and rehabilitation tactics in MS patients.
基本原理。行走和平衡障碍、足部肌肉运动紊乱和行走刻板印象是多发性硬化症(MS)患者的典型症状。评估不同神经系统状态MS患者行走时足部生物力学参数。材料和方法。根据扩展残疾状态量表(EDSS)的值对两组102例复发-缓解型MS患者进行数据分析。采用“第一步”方案,在德国慕尼黑新颖gmbh公司的测量平台上测量足底压力分布。结果与结论。在MS患者行走时,脚跟的负荷,跖骨中央头部的面积减少,脚趾的负荷增加。在扩展系数(足宽与足长之比)上发现差异,EDSS≥4的患者的足部动态宽度在脚背、足中部和足部最窄处明显减小,导致接触面积减小。研究表明,与有轻微损伤的多发性硬化症患者相比,能够活动或无需辅助行走的多发性硬化症患者更容易患足弓足。足内侧的负荷大于外侧,说明外翻足占主导地位。在脱趾期,中度损伤患者的旋前指数明显增高。通过测量足底压力分布的生物力学参数来评估足部畸形,为MS患者制定治疗和康复策略提供了可能。
{"title":"Assessment of biomechanical parameters of feet in patients with multiple sclerosis during walking","authors":"A. D. Dorokhov, E. V. Ivashkova, A. G. Ilves, K. K. Mineev, I. G. Negoreeva, A. M. Petrov, L. N. Prakhova, I. D. Stolyarov, G. G. Shkilnyuk, V. N. Tartakovskiy, T. L. Tcvetkova, V. A. Zubarev","doi":"10.30629/2658-7947-2023-28-4-35-42","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-4-35-42","url":null,"abstract":"Rationale. Walking and balance disorders, modi fi ed foot muscles kinematics and walking stereotypes are typical for the patients with Multiple Sclerosis (MS).Objective. To assess the biomechanical parameters of the feet in MS patients with diff erent neurological status during walking.Material and methods. Data analysis of 102 patients with relapsing-remitting MS was carried out for two groups depending on the value of the Expanded Disability Status Scale (EDSS). Plantar pressure distribution was measured on with the pedographic platform emed, novel gmbh, Munich, Germany, using a “fi rst step” protocol.Results and conclusion. Loading of the heel, the area of central metatarsal heads is decreased and loading of the toes is increased during walking in MS patients. Diff erences were found for the spreading coeffi cient (the ratio of the width to the length of the foot), the dynamic width of the foot in patients with an EDSS ≥ 4 is signi fi cantly less in the instep, in the middle and in the narrowest parts of the foot, which leads to the decrease of the contact area. It has been shown that patients with MS who are mobile or walk without assistance are more likely to have pes cavus foot compared to MS patients with minor impairments. The load of the medial side of the foot is greater than the lateral side, which indicates the predominance of the valgus foot. The pronation-supination index is signi fi cantly higher in the patients with moderate impairments in toe-off phase. Evaluation of foot deformity based on the measurement of biomechanical parameters of plantar pressure distribution makes it possible to plan the treatment and rehabilitation tactics in MS patients.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":"151 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135900152","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
Neuroimaging in facial nerve neuropathy 面神经病变的神经影像学
Q4 Medicine Pub Date : 2023-09-30 DOI: 10.30629/2658-7947-2023-28-4-24-34
S. S. Petrikov, N. A. Shamalov, L. B. Zavaliy, O. L. Evdokimova, M. V. Neznanova, I. A. Tyrov, A. N. Koriagin, A. G. Fomkin, D. V. Kuular, T. A. Nikulina
The timing and volume of neuroimaging for patients with facial nerve neuropathy (FNN) are a cause for discussion. Aim. To study the current volume of neuroimaging in patients with FNN and to determine the essential diagnostic protocol. Material and methods. Magnetic resonance imaging (MRI) data analysis of adult patients with FNN (n = 833). Protocols were taken from the Uni fi ed Medical Information and Analytical System of Moscow (EMIAS). The essential diagnostic protocol was created. A prospective study was conducted with new protocol. Results. According to EMIAS, the timing of MRI was 3 months from the fi rst symptoms to do diagnostics, the longest period from diagnosis to appointment to MRI was 83 days. The list of pulse sequences was given in the protocol in ¾ of cases. The most indicated regimes were T1 WI (80.7%), T2 WI (90.6%), T2 FLAIR (73.2%), less often DWI (54.9%). Studies with contrast amounted to 22.8%. In total, the pathology was detected in 429 (51.5%) patients, including 88 (20.5%) intracranial tumors. In 216 (25.9%) patients, the changes were most likely associated with FNN, of which in 44.5% of cases were in fl ammatory, 21.3% — tumor, 16.2% — demyelinating process, 11.2% — postoperative changes. According to the new protocol, the cause of FNN was directly identi fi ed in 56.6% of patients, of which in idiopathic — 31,6% of cases, in symptomatic — 70.6% (p = 0.005). Changes that cannot be associated with FNN, but require the participation of a specialist, were detected in a 1/4 of patients. Only in 20.8% of cases, the MRI results were normal. Conclusion. Recommended volume of neuroimaging for patients with FNN is MRI of the brain and parotid salivary glands with contrast within 1 month from the fi st symptoms. Regimes: T1 WI, T2 WI, FLAIR (with a slice thickness of 1 mm), DWI, 3D TOF, free recession in equilibrium (SSFP, FIESTA-C, CISS, FFE, etc.), sensitive to magnetic fi eld inhomogeneity (T2*, SWI, SWAN, etc.), and also T1 WI after intravenous contrast.
面神经病变(FNN)患者的神经显像时机和体积是一个值得讨论的问题。的目标。研究FNN患者目前的神经影像量,并确定必要的诊断方案。材料和方法。成年FNN患者的磁共振成像(MRI)资料分析(n = 833)。协议取自莫斯科统一医疗信息和分析系统(EMIAS)。基本的诊断方案被创建。采用新方案进行前瞻性研究。结果。根据EMIAS,从首次出现症状到进行诊断,MRI的时间为3个月,从诊断到预约再到MRI的最长时间为83天。四分之三的病例的治疗方案中给出了脉冲序列列表。最常见的是T1 WI (80.7%), T2 WI (90.6%), T2 FLAIR(73.2%),较少的是DWI(54.9%)。造影剂研究占22.8%。其中颅内肿瘤88例(20.5%),病理检出429例(51.5%)。216例(25.9%)患者的改变最可能与FNN相关,其中44.5%的病例为炎性,21.3%为肿瘤,16.2%为脱髓鞘过程,11.2%为术后改变。根据新方案,56.6%的患者可直接诊断出FNN的病因,其中特发性为31.6%,症状性为70.6% (p = 0.005)。在1/4的患者中发现了与FNN无关但需要专家参与的变化。仅20.8%的病例MRI结果正常。结论。对于FNN患者,推荐的神经影像学检查是在首次出现症状后1个月内对大脑和腮腺涎腺进行MRI对比检查。检查机制:T1 WI、T2 WI、FLAIR(片厚1mm)、DWI、3D TOF、平衡自由衰退(SSFP、fista - c、CISS、FFE等)、对磁场不均匀性敏感(T2*、SWI、SWAN等),以及静脉造影术后的T1 WI。
{"title":"Neuroimaging in facial nerve neuropathy","authors":"S. S. Petrikov, N. A. Shamalov, L. B. Zavaliy, O. L. Evdokimova, M. V. Neznanova, I. A. Tyrov, A. N. Koriagin, A. G. Fomkin, D. V. Kuular, T. A. Nikulina","doi":"10.30629/2658-7947-2023-28-4-24-34","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-4-24-34","url":null,"abstract":"The timing and volume of neuroimaging for patients with facial nerve neuropathy (FNN) are a cause for discussion. Aim. To study the current volume of neuroimaging in patients with FNN and to determine the essential diagnostic protocol. Material and methods. Magnetic resonance imaging (MRI) data analysis of adult patients with FNN (n = 833). Protocols were taken from the Uni fi ed Medical Information and Analytical System of Moscow (EMIAS). The essential diagnostic protocol was created. A prospective study was conducted with new protocol. Results. According to EMIAS, the timing of MRI was 3 months from the fi rst symptoms to do diagnostics, the longest period from diagnosis to appointment to MRI was 83 days. The list of pulse sequences was given in the protocol in ¾ of cases. The most indicated regimes were T1 WI (80.7%), T2 WI (90.6%), T2 FLAIR (73.2%), less often DWI (54.9%). Studies with contrast amounted to 22.8%. In total, the pathology was detected in 429 (51.5%) patients, including 88 (20.5%) intracranial tumors. In 216 (25.9%) patients, the changes were most likely associated with FNN, of which in 44.5% of cases were in fl ammatory, 21.3% — tumor, 16.2% — demyelinating process, 11.2% — postoperative changes. According to the new protocol, the cause of FNN was directly identi fi ed in 56.6% of patients, of which in idiopathic — 31,6% of cases, in symptomatic — 70.6% (p = 0.005). Changes that cannot be associated with FNN, but require the participation of a specialist, were detected in a 1/4 of patients. Only in 20.8% of cases, the MRI results were normal. Conclusion. Recommended volume of neuroimaging for patients with FNN is MRI of the brain and parotid salivary glands with contrast within 1 month from the fi st symptoms. Regimes: T1 WI, T2 WI, FLAIR (with a slice thickness of 1 mm), DWI, 3D TOF, free recession in equilibrium (SSFP, FIESTA-C, CISS, FFE, etc.), sensitive to magnetic fi eld inhomogeneity (T2*, SWI, SWAN, etc.), and also T1 WI after intravenous contrast.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":"28 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136344748","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
Cervical dystonia: ways to achieve long-term treatment eff ects and improve patients’ quality of life 颈张力障碍:如何达到长期的治疗效果,提高患者的生活质量
Q4 Medicine Pub Date : 2023-09-30 DOI: 10.30629/2658-7947-2023-28-4-16-23
N. I. Salouhina, M. R. Nodel, V. A. Tolmacheva
The main treatment for cervical dystonia (CD) is botulinum toxin type A (BTA) injections, but several long-term studies have found that between 19-46% of patients discontinue treatment. Anxiety and depression play a signi fi cant role in reducing the quality of life in patients with CD, according to previous surveys.Aim: to assess the dynamics of CD symptom severity, emotional disturbance, and quality of life in patients under different treatment methods.Material and methods. 61 patients with CD, 16 (26%) men and 45 (74%) women, age 50 [40; 59] years, duration of illness 4 [2; 7] years, age at onset 44 [34; 54] years, were studied. Changes in motor and aff ective disturbances, quality of life in patients with CD were assessed after 2 and 4 months in the context of diff erent treatment methods — BTA monotherapy, antidepressant (AD), combined therapy (AD + AD).Results. Combination therapy (BT + AD) was shown to be superior to BTA monotherapy in long-term follow-up of patients in terms of correction of depression, anxiety, integrative assessment of quality of life and severity of dystonia. After 4 months of treatment, the (BT + AD) subgroup maintained the positive trend achieved in dystonia severity (p < 0.001). At the end of the follow-up period in the BT group, the positive eff ect of therapy had regressed to baseline levels of dystonia severity.Conclusion. To achieve a sustained therapeutic response in patients with CD, diagnosis and appropriate correction of emotional disturbances is necessary. The potential effi cacy of antidepressants in the treatment of motor and sensory symptoms of CD requires further investigation.
宫颈肌张力障碍(CD)的主要治疗方法是注射A型肉毒杆菌毒素(BTA),但几项长期研究发现,19-46%的患者停止治疗。根据先前的调查,焦虑和抑郁在降低乳糜泻患者的生活质量中起着重要的作用。目的:评价不同治疗方法对乳糜泻患者症状严重程度、情绪障碍及生活质量的影响。材料和方法。61例CD患者,男性16例(26%),女性45例(74%),年龄50 [40];59岁,病程4 [2];7]岁,发病年龄44岁[34;[54]年,进行了研究。在不同的治疗方法- BTA单药治疗、抗抑郁药(AD)、联合治疗(AD + AD)的情况下,在2个月和4个月后评估CD患者的运动和情绪障碍、生活质量的变化。结果。在对患者的长期随访中,BT + AD联合治疗在纠正抑郁、焦虑、生活质量综合评估和肌张力障碍严重程度方面均优于BTA单药治疗。治疗4个月后,(BT + AD)亚组在肌张力障碍严重程度方面保持阳性趋势(p <0.001)。在BT组的随访期结束时,治疗的积极影响已经回归到肌张力障碍严重程度的基线水平。结论。为了使乳糜泻患者获得持续的治疗反应,诊断和适当纠正情绪障碍是必要的。抗抑郁药治疗乳糜泻运动和感觉症状的潜在疗效有待进一步研究。
{"title":"Cervical dystonia: ways to achieve long-term treatment eff ects and improve patients’ quality of life","authors":"N. I. Salouhina, M. R. Nodel, V. A. Tolmacheva","doi":"10.30629/2658-7947-2023-28-4-16-23","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-4-16-23","url":null,"abstract":"The main treatment for cervical dystonia (CD) is botulinum toxin type A (BTA) injections, but several long-term studies have found that between 19-46% of patients discontinue treatment. Anxiety and depression play a signi fi cant role in reducing the quality of life in patients with CD, according to previous surveys.Aim: to assess the dynamics of CD symptom severity, emotional disturbance, and quality of life in patients under different treatment methods.Material and methods. 61 patients with CD, 16 (26%) men and 45 (74%) women, age 50 [40; 59] years, duration of illness 4 [2; 7] years, age at onset 44 [34; 54] years, were studied. Changes in motor and aff ective disturbances, quality of life in patients with CD were assessed after 2 and 4 months in the context of diff erent treatment methods — BTA monotherapy, antidepressant (AD), combined therapy (AD + AD).Results. Combination therapy (BT + AD) was shown to be superior to BTA monotherapy in long-term follow-up of patients in terms of correction of depression, anxiety, integrative assessment of quality of life and severity of dystonia. After 4 months of treatment, the (BT + AD) subgroup maintained the positive trend achieved in dystonia severity (p < 0.001). At the end of the follow-up period in the BT group, the positive eff ect of therapy had regressed to baseline levels of dystonia severity.Conclusion. To achieve a sustained therapeutic response in patients with CD, diagnosis and appropriate correction of emotional disturbances is necessary. The potential effi cacy of antidepressants in the treatment of motor and sensory symptoms of CD requires further investigation.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":"162 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136343943","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
Symptom of vertigo and dizziness in patients with COVID-19 新冠肺炎患者的眩晕和头晕症状
Q4 Medicine Pub Date : 2023-09-30 DOI: 10.30629/2658-7947-2023-28-4-5-15
E. V. Isakova
The symptom of vertigo and dizziness is often detected in patients with COVID-19. The article discusses issues related to damage to the peripheral and vestibular parts of the vestibular analyzer in patients infected with the SARS-CoV-2 virus. The possible mechanisms of the pathogenesis of the development of cerebral stroke in this viral infection, its features are described. A description of the forms of damage to the peripheral part of the vestibular analyzer, including vestibular neuronitis, benign paroxysmal positional vertigo, Meniere’s disease, is presented. Other possible causes of the development of the symptom of vertigo and dizziness in patients with COVID-19 that are not associated with damage to the vestibular analyzer are also considered
新冠肺炎患者常出现眩晕和头晕症状。本文讨论了SARS-CoV-2病毒感染患者前庭分析仪外周和前庭部分损伤的相关问题。脑中风在这种病毒感染发展的可能的发病机制,其特点进行了描述。描述的形式损害的外围部分的前庭分析器,包括前庭神经炎,良性阵发性位置性眩晕,梅尼埃病,提出。还考虑了与前庭分析仪损伤无关的COVID-19患者眩晕和头晕症状发展的其他可能原因
{"title":"Symptom of vertigo and dizziness in patients with COVID-19","authors":"E. V. Isakova","doi":"10.30629/2658-7947-2023-28-4-5-15","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-4-5-15","url":null,"abstract":"The symptom of vertigo and dizziness is often detected in patients with COVID-19. The article discusses issues related to damage to the peripheral and vestibular parts of the vestibular analyzer in patients infected with the SARS-CoV-2 virus. The possible mechanisms of the pathogenesis of the development of cerebral stroke in this viral infection, its features are described. A description of the forms of damage to the peripheral part of the vestibular analyzer, including vestibular neuronitis, benign paroxysmal positional vertigo, Meniere’s disease, is presented. Other possible causes of the development of the symptom of vertigo and dizziness in patients with COVID-19 that are not associated with damage to the vestibular analyzer are also considered","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":"36 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136343942","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
Clinical case of hypertrophic convexital pachymeningitis 增生性凸性厚性脑膜炎1例
Q4 Medicine Pub Date : 2023-07-19 DOI: 10.30629/2658-7947-2023-28-3-55-60
V. V. Ponomarev, T. A. Rakot
A clinical analysis of a patient with undifferentiated granulomatous systemic vasculitis with a predominant lung lesion and its complication in the form of chronic hypertrophic convexital pachymeningitis of fungal (candidal) etiology is presented. A differential diagnosis with granulomatosis with polyangiitis was carried out. Modern literature data on diagnostic criteria and methods of treatment of this rare pathology are given.
本文报告1例以肺部病变为主的未分化肉芽肿性全身性血管炎,并发真菌(念珠菌)所致的慢性肥厚性凸性肿性脑膜炎。鉴别诊断为肉芽肿病合并多血管炎。现代文献资料的诊断标准和治疗方法,这种罕见的病理给出。
{"title":"Clinical case of hypertrophic convexital pachymeningitis","authors":"V. V. Ponomarev, T. A. Rakot","doi":"10.30629/2658-7947-2023-28-3-55-60","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-3-55-60","url":null,"abstract":"A clinical analysis of a patient with undifferentiated granulomatous systemic vasculitis with a predominant lung lesion and its complication in the form of chronic hypertrophic convexital pachymeningitis of fungal (candidal) etiology is presented. A differential diagnosis with granulomatosis with polyangiitis was carried out. Modern literature data on diagnostic criteria and methods of treatment of this rare pathology are given.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42694016","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
Magnetic resonance morphometry of the brain volume, medial temporal lobes and hippocampus in middle-aged patients with premild cognitive decline 中年早期认知能力下降患者大脑体积、内侧颞叶和海马的磁共振形态测量
Q4 Medicine Pub Date : 2023-07-19 DOI: 10.30629/2658-7947-2023-28-3-22-27
N. Koberskaya, V. Perepelov, D. Smirnov, V. Gridin, N. Yakhno
Currently, instrumental brain imaging plays a significant role in the examination of patients with cognitive impairment. It is important for diagnostic process, prognosis of the course of neurodegenerative, cerebrovascular and other diseases, clarification of the role of individual brain structures and systems in the development of cognitive and other neuropsychiatric disorders.The purpose of the study was to analyze the volumes of the medial temporal lobes (MTL), hippocampus and brain volume in middle-aged patients with pre-mild cognitive decline.Material and methods. 38 patients (33 women, 5 men) of middle age (60.77 ± 9.4 years) were examined. Patients were divided into two groups: with subjective cognitive decline (SCD) – 15 patients, aged 53.5 ± 6.94 years and subtle cognitive decline (StCD) – 23 people aged 63.35 ± 8.64 years (groups statistically did not differ in age). All patients underwent a neuropsychological examination with an assessment of the cognitive sphere, magnetic resonance imaging of the brain, including the assessment of the presence and degree of microangiopathy (MAP), morphometry of the medial temporal lobes, hippocampus, brain volume and a study for the presence of the allele of the apolyprotein E gene (ApoE4).Results. A decrease in the average and total hippocampal volume was found in patients with StCD compared to patients with SCD. Also, MAP was significantly more common in patients with StCD. There were no differences in the degree of MTL atrophy. A decrease in the volume of the left hippocampus was revealed in patients with aggravated heredity for dementia. The average and total volume of the hippocampus is reduced in carriers of the ApoE4 allele of the apolyprotein gene. Correlation analysis showed the relationship between the average volume of the hippocampus and the volume of the brain.
目前,仪器脑成像在认知障碍患者的检查中发挥着重要作用。这对于神经退行性、脑血管等疾病的诊断和预后,阐明个体脑结构和系统在认知和其他神经精神疾病发展中的作用具有重要意义。本研究的目的是分析中度认知衰退的中年患者的内侧颞叶(MTL)、海马和脑容量。材料和方法。38例中年患者(60.77±9.4岁),女33例,男5例。患者分为主观认知能力下降组(SCD) 15例,年龄53.5±6.94岁;轻度认知能力下降组(StCD) 23例,年龄63.35±8.64岁(两组年龄无统计学差异)。所有患者都接受了神经心理学检查,包括认知领域评估、脑磁共振成像,包括评估微血管病变(MAP)的存在和程度、内侧颞叶、海马、脑容量的形态测定和载脂蛋白E基因(ApoE4)等位基因存在的研究。与SCD患者相比,StCD患者的平均海马体积和总海马体积减小。此外,MAP在性传播疾病患者中更为常见。两组间颞叶萎缩程度无差异。在遗传加重的痴呆症患者中,左侧海马体的体积减少。携带载脂蛋白基因ApoE4等位基因的海马平均体积和总体积减小。相关分析显示海马的平均体积与大脑的体积之间存在相关性。
{"title":"Magnetic resonance morphometry of the brain volume, medial temporal lobes and hippocampus in middle-aged patients with premild cognitive decline","authors":"N. Koberskaya, V. Perepelov, D. Smirnov, V. Gridin, N. Yakhno","doi":"10.30629/2658-7947-2023-28-3-22-27","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-3-22-27","url":null,"abstract":"Currently, instrumental brain imaging plays a significant role in the examination of patients with cognitive impairment. It is important for diagnostic process, prognosis of the course of neurodegenerative, cerebrovascular and other diseases, clarification of the role of individual brain structures and systems in the development of cognitive and other neuropsychiatric disorders.The purpose of the study was to analyze the volumes of the medial temporal lobes (MTL), hippocampus and brain volume in middle-aged patients with pre-mild cognitive decline.Material and methods. 38 patients (33 women, 5 men) of middle age (60.77 ± 9.4 years) were examined. Patients were divided into two groups: with subjective cognitive decline (SCD) – 15 patients, aged 53.5 ± 6.94 years and subtle cognitive decline (StCD) – 23 people aged 63.35 ± 8.64 years (groups statistically did not differ in age). All patients underwent a neuropsychological examination with an assessment of the cognitive sphere, magnetic resonance imaging of the brain, including the assessment of the presence and degree of microangiopathy (MAP), morphometry of the medial temporal lobes, hippocampus, brain volume and a study for the presence of the allele of the apolyprotein E gene (ApoE4).Results. A decrease in the average and total hippocampal volume was found in patients with StCD compared to patients with SCD. Also, MAP was significantly more common in patients with StCD. There were no differences in the degree of MTL atrophy. A decrease in the volume of the left hippocampus was revealed in patients with aggravated heredity for dementia. The average and total volume of the hippocampus is reduced in carriers of the ApoE4 allele of the apolyprotein gene. Correlation analysis showed the relationship between the average volume of the hippocampus and the volume of the brain.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42735169","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
Kinesiotherapy in chronic back pain and combined tension type headache 运动疗法治疗慢性背痛和合并紧张性头痛
Q4 Medicine Pub Date : 2023-07-19 DOI: 10.30629/2658-7947-2023-28-3-61-68
A. A. Golovacheva, V. Golovacheva
Kinesiotherapy is eff ective in the treatment of chronic nonspecific back pain (CNBP), but its eff ectiveness in tensiontype headache (TTH) is unclear. The effectiveness of kinesiotherapy in patients with CNBP and comorbid TTH has been little studied.The aim of the study was to evaluate the effectiveness of kinesiotherapy in patients with CNBS and comorbid TTH. Patients and methods. 52 patients (22 men and 30 women, mean age 32.4 ± 7.5 years) with CNBP and combined TTH were included in the study. All patients received standard treatment, of which 28 patients received kinesiotherapy (Group 1) and 24 patients were included in the comparison group (Group 2). All patients used pain diaries. All patients were tested by using the Beck Anxiety Inventory, the Beck’s Depression Inventory, the Pain Catastrophization Scale, the Kinesiophobia Scale, the Oswestry Disability Index, the Roland–Morris Disability Questionnaire, the Headache Impact Test 6, numerical pain rating scale before treatment and 3, 6 months after treatment. Clinical effcacy was assessed by reducing the frequency and intensity of headache (by ≥ 50%), back pain (by ≥ 30%), and by increasing functional activity during the day (by ≥ 30%).Results. At 6 months follow-up signifiantly more patients in group 1 than in group 2 achieved a clinical effect on TTH and CNBP: 78.5% (n = 22) compared to 41.7% (n = 10); OR (95% CI) = 1.99. In 9 patients (32%) of group 1, a complete remission of TTH and CNBP was noted, in group 2 there were no such patients. At 6 months follow-up group 1 showed a significant improvement (p < 0.05) in comparison with group 2 in terms of functional activity and emotional state.Conclusion. Kinesiotherapy for CNBP and combined TTH is effective both for back pain and headache. It increases functional activity and improves the emotional state of patients.
运动疗法是有效的治疗慢性非特异性背痛(CNBP),但其有效性在紧张性头痛(TTH)尚不清楚。运动疗法对CNBP合并TTH患者的疗效研究甚少。该研究的目的是评估运动疗法对CNBS合并TTH患者的有效性。患者和方法。纳入52例CNBP合并TTH患者(男22例,女30例,平均年龄32.4±7.5岁)。所有患者均接受标准治疗,其中28例患者接受运动疗法(第一组),24例患者作为对照组(第二组)。所有患者均使用疼痛日记。所有患者在治疗前和治疗后3、6个月分别采用Beck焦虑量表、Beck抑郁量表、疼痛灾难化量表、运动恐惧症量表、Oswestry残疾指数、Roland-Morris残疾问卷、头痛影响测试6、数值疼痛评定量表进行测试。临床疗效通过减少头痛的频率和强度(≥50%)、背部疼痛(≥30%)和增加白天的功能活动(≥30%)来评估。在6个月的随访中,1组患者TTH和CNBP的临床疗效显著高于2组:78.5% (n = 22)对41.7% (n = 10);或(95% ci) = 1.99。1组9例患者(32%)TTH和CNBP完全缓解,2组无此类患者。随访6个月时,组1在功能活动和情绪状态方面较组2有显著改善(p < 0.05)。运动疗法治疗CNBP和联合TTH对背痛和头痛都有效。它增加了患者的功能活动,改善了患者的情绪状态。
{"title":"Kinesiotherapy in chronic back pain and combined tension type headache","authors":"A. A. Golovacheva, V. Golovacheva","doi":"10.30629/2658-7947-2023-28-3-61-68","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-3-61-68","url":null,"abstract":"Kinesiotherapy is eff ective in the treatment of chronic nonspecific back pain (CNBP), but its eff ectiveness in tensiontype headache (TTH) is unclear. The effectiveness of kinesiotherapy in patients with CNBP and comorbid TTH has been little studied.The aim of the study was to evaluate the effectiveness of kinesiotherapy in patients with CNBS and comorbid TTH. Patients and methods. 52 patients (22 men and 30 women, mean age 32.4 ± 7.5 years) with CNBP and combined TTH were included in the study. All patients received standard treatment, of which 28 patients received kinesiotherapy (Group 1) and 24 patients were included in the comparison group (Group 2). All patients used pain diaries. All patients were tested by using the Beck Anxiety Inventory, the Beck’s Depression Inventory, the Pain Catastrophization Scale, the Kinesiophobia Scale, the Oswestry Disability Index, the Roland–Morris Disability Questionnaire, the Headache Impact Test 6, numerical pain rating scale before treatment and 3, 6 months after treatment. Clinical effcacy was assessed by reducing the frequency and intensity of headache (by ≥ 50%), back pain (by ≥ 30%), and by increasing functional activity during the day (by ≥ 30%).Results. At 6 months follow-up signifiantly more patients in group 1 than in group 2 achieved a clinical effect on TTH and CNBP: 78.5% (n = 22) compared to 41.7% (n = 10); OR (95% CI) = 1.99. In 9 patients (32%) of group 1, a complete remission of TTH and CNBP was noted, in group 2 there were no such patients. At 6 months follow-up group 1 showed a significant improvement (p < 0.05) in comparison with group 2 in terms of functional activity and emotional state.Conclusion. Kinesiotherapy for CNBP and combined TTH is effective both for back pain and headache. It increases functional activity and improves the emotional state of patients.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48430108","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
The probability of achieving remission after correction of therapy in patients with pharmacoresistant focal epilepsy 顽固性局灶性癫痫患者纠正治疗后获得缓解的可能性
Q4 Medicine Pub Date : 2023-07-19 DOI: 10.30629/2658-7947-2023-28-3-36-43
K. V. Firsov, A. Kotov, M. G. Amirchanyan
Drug-resistant forms of epilepsy are an important medical and social problem.Goal of the work. Evaluation of the probability of achieving remission after correction of therapy in patients with drug-resistant focal epilepsy.Material and methods. The study included 309 patients divided into three heterogeneous groups: a group of patients with focal pharmacoresistant epilepsy; a group of patients with super refractory focal epilepsy; control group – patients who had not previously received treatment. The examination included history taking, clinical and neurological examination, routine EEG and/or EEG video monitoring, MRI of the brain, and analysis of medical records. Therapy was adjusted.Results. After correction of therapy, remission in patients in Group 1 was achieved in 27.8% of patients, improvement – in 27.1%, no effect – in 45.1%; in Group 2, remission was achieved in 13.2% of patients, improvement – in 28.6%, no effect – in 58.2%; in Group 3, remission was achieved in 41.2% of patients, improvement – in 32.9%, no effect – in 25.9%. Negative prognostic factors did not show a significant correlation with the lack of effect of therapy.Conclusion. After correction of therapy, remission was achieved in several patients with drug-resistant focal epilepsy, while negative prognostic factors do not exclude the possibility of achieving remission.
耐药癫痫是一个重要的医学和社会问题。工作目标。评价耐药局灶性癫痫患者矫正治疗后获得缓解的可能性。材料和方法。该研究将309例患者分为三组:局灶性耐药癫痫患者组;一组超难治性局灶性癫痫患者;对照组为未接受过治疗的患者。检查包括病史记录、临床和神经学检查、常规脑电图和/或脑电图视频监测、脑部核磁共振成像和医疗记录分析。调整治疗方法。纠正治疗后,第1组有27.8%的患者缓解,27.1%的患者改善,45.1%的患者无效果;在第二组,13.2%的患者缓解,28.6%的患者改善,58.2%的患者无效果;在第三组,41.2%的患者缓解,32.9%的患者改善,25.9%的患者无效果。不良预后因素与治疗效果不明显相关。在纠正治疗后,一些耐药局灶性癫痫患者的病情得到缓解,但负面预后因素并不排除缓解的可能性。
{"title":"The probability of achieving remission after correction of therapy in patients with pharmacoresistant focal epilepsy","authors":"K. V. Firsov, A. Kotov, M. G. Amirchanyan","doi":"10.30629/2658-7947-2023-28-3-36-43","DOIUrl":"https://doi.org/10.30629/2658-7947-2023-28-3-36-43","url":null,"abstract":"Drug-resistant forms of epilepsy are an important medical and social problem.Goal of the work. Evaluation of the probability of achieving remission after correction of therapy in patients with drug-resistant focal epilepsy.Material and methods. The study included 309 patients divided into three heterogeneous groups: a group of patients with focal pharmacoresistant epilepsy; a group of patients with super refractory focal epilepsy; control group – patients who had not previously received treatment. The examination included history taking, clinical and neurological examination, routine EEG and/or EEG video monitoring, MRI of the brain, and analysis of medical records. Therapy was adjusted.Results. After correction of therapy, remission in patients in Group 1 was achieved in 27.8% of patients, improvement – in 27.1%, no effect – in 45.1%; in Group 2, remission was achieved in 13.2% of patients, improvement – in 28.6%, no effect – in 58.2%; in Group 3, remission was achieved in 41.2% of patients, improvement – in 32.9%, no effect – in 25.9%. Negative prognostic factors did not show a significant correlation with the lack of effect of therapy.Conclusion. After correction of therapy, remission was achieved in several patients with drug-resistant focal epilepsy, while negative prognostic factors do not exclude the possibility of achieving remission.","PeriodicalId":36724,"journal":{"name":"Russian Neurological Journal","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44646431","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
期刊
Russian Neurological Journal
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1