امروز: دوشنبه, 7 مهر , 1399


مرکز تحقیقات مغز واعصاب تهران

Papers

Iranian Center of Neurological Research Articles

From 2016  to Present

 

2018


A novel combination of ω-3 fatty acids and nano-curcumin modulates interleukin-6 gene expression and high sensitivity C-reactive protein serum levels in patients with migraine: a randomized clinical trial study


Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population


Loud, non-stethoscope audible pulsatile tinnitus and papilledema: A rare presentation of dural arteriovenous fistula


A genetic study of celiac disease in patients with multiple sclerosis in comparison with celiac patients and healthy controls


Transplantation of olfactory ensheathing cells on functional recovery and neuropathic pain after spinal cord injury; Systematic review and meta-analysis


Does oral administration of ketamine accelerate response to treatment in major depressive disorder? Results of a double-blind controlled trial


Multiple sclerosis pathogenesis: Missing pieces of an old puzzle


Immunomodulatory function of Treg-derived exosomes is impaired in patients with relapsing-remitting multiple sclerosis


B cells in multiple sclerosis therapy—A comprehensive review


A presentation of ulcerative colitis after rituximab therapy in a patient with multiple sclerosis and literature review


Biphasic effect of sumatriptan on PTZ-induced seizures in mice: Modulation by 5-HT1B/D receptors and NOS/NO pathway


A case of dextrocardia following maternal exposure to generic Fingolimod during the first trimester of pregnancy


Differential Expression of Klotho in the Brain and Spinal Cord is Associated with Total Antioxidant Capacity in Mice with Experimental Autoimmune Encephalomyelitis


A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations


Evaluation of regulatory T lymphocytes and IL2Ra and FOXP3 gene expression in peripheral mononuclear cells from patients with amyotrophic lateral sclerosis


Increased Proportion of Tc17 and Th17 Cells and Their Significant Reduction after Thymectomy May Be Related to Disease Progression in Myasthenia Gravis


Cerebral Hyperperfusion Syndrome, an Unusual but Disastrous Complication of Carotid Recanalization: A Case Report


Worldwide prevalence of familial multiple sclerosis: A systematic review and meta-analysis


Genetic screening in two Iranian families with early-onset Alzheimer’s disease identified a novel PSEN1 mutation


Convergent effects of a functional C3 variant on brain atrophy, demyelination, and cognitive impairment in multiple sclerosis


Safety and Efficacy of Nanocurcumin as Add-On Therapy to Riluzole in Patients With Amyotrophic Lateral Sclerosis: A Pilot Randomized Clinical Trial


Bariatric Surgery Promising in Migraine Control: a Controlled Trial on Weight Loss and Its Effect on Migraine Headache


Osteopontin (OPN) as a CSF and blood biomarker for multiple sclerosis: A systematic review and meta-analysis


Comorbidity of gastrointestinal disorders, migraine, and tension-type headache: a cross-sectional study in Iran


2017


The combined effects of ω -3 fatty acids and nano-curcumin supplementation on intercellular adhesion molecule-1 (ICAM-1) gene expression and serum levels in migraine patients


Whole genome sequencing identifies a novel homozygous exon deletion in the NT5C2 gene in a family with intellectual disability and spastic paraplegia


Potential diagnostic value of131I-MIBG myocardial scintigraphy in discrimination between Alzheimer disease and dementia with Lewy bodies


Genetic analysis of SNCA gene polymorphisms in Parkinson’s disease in an Iranian population


A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome


Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome


Diagnosis and management of Neuromyelitis Optica Spectrum Disorder (NMOSD) in Iran: A consensus guideline and recommendations


MLC601 in vascular dementia: An efficacy and safety pilot study


Effect of ischemic compression for cervicogenic headache and elastic behavior of active trigger point in the sternocleidomastoid muscle using ultrasound imaging


Metalloproteinase 9 as a biomarker of progressive multifocal leukoencephalopathy development in multiple sclerosis patients receiving natalizumab


A robust beamforming approach for early detection of readiness potential with application to brain-computer interface systems


Pyridostigmine-Induced Bradycardia in Patient with MuSK-Ab-Positive Myasthenia Gravis and Alopecia Universalis


De novo mutation in CACNA1S gene in a 20-year-old man diagnosed with metabolic myopathy


Compound heterozygosity in the GALC gene in a late onset Iranian patient with spastic paraparesis, peripheral neuropathy and leukoencephalopathy


Long-term follow-up of MRI changes in thigh muscles of patients with Facioscapulohumeral dystrophy: A quantitative study


Mendelian Genes and Risk of Intracerebral Hemorrhage and Small-Vessel Ischemic Stroke in Sporadic Cases


Evaluating executive function in patients with temporal lobe epilepsy using the frontal assessment battery


Validation of the Persian Version of the Brief Pain Inventory (BPI-P) in Chronic Pain Patients


A giant cervicothoracic cord lipoma: an uncommon finding


Late-onset pompe disease in Iran: A clinical and genetic report


The synergistic effects of ω-3 fatty acids and nano-curcumin supplementation on tumor necrosis factor (TNF)-α gene expression and serum level in migraine patients


Rapamycin Augments Immunomodulatory Properties of Bone Marrow-Derived Mesenchymal Stem Cells in Experimental Autoimmune Encephalomyelitis


RIT2 Polymorphisms: Is There a Differential Association?


The expression of lnc-IL-7R long non-coding RNA dramatically correlated with soluble and membrane-bound isoforms of IL-7Ra gene in multiple sclerosis patients


Metronidazole-induced neurotoxicity presenting with sudden bilateral hearing loss, encephalopathy, and cerebellar dysfunction


PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism


Personality traits and anxiety and depressive disorders in patients with medication-overuse headache versus episodic migraine


Thymic carcinoma developing years after thymectomy


Comparison of two different PCR-based methods for detection of GAA expansions in frataxin gene


Prediction of clinically important traumatic brain injury in pediatric minor head trauma; proposing pediatric traumatic brain injury (PTBI) prognostic rule


A case based-shared teaching approach in undergraduate medical curriculum: A way for integration in basic and clinical sciences


Early versus late decompression for traumatic spinal cord injuries; a systematic review andmeta-analysis


Sensing of Alzheimer’s disease and multiple sclerosis using nano-bio interfaces


2016


Cerebral Venous Sinus Thrombosis May Follow a Seasonal Pattern


Diagnostic laboratory challenges about Charcot-Marie-Tooth disease


Paracetamol 325 mg/tramadol 37.5 mg effect on pain during needle electromyography: a double-blind crossover clinical trial


Headache in Behcet’s disease: types and characteristics


Impaired arterial smooth muscle cell vasodilatory function in methamphetamine users


Efficacy and safety of oral ketamine versus diclofenac to alleviate mild to moderate depression in chronic pain patients: A double-blind, randomized, controlled trial


The role of Candida albicans in the severity of multiple sclerosis


Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism


SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson’s diseases in Iranian population: A case-control study


Quality of Life in Medical Students With Internet Addiction



Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson’s Disease in the Iranian Population


Muscle MRI of facioscapulohumeral dystrophy (FSHD): A growing demand and a promising approach


Trends of quality of life changes in amyotrophic lateral sclerosis patients


Pharmacogenetic Study on the Impact of Rivastigmine Concerning Genetic Variants of A2M and IL-6 Genes on Iranian Alzheimer’s Patients


Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage


Validation of the 15-item myasthenia gravis quality of life questionnaire (MG-QOL15) Persian version


Retinyl Palmitate Supplementation Modulates T-bet and Interferon Gamma Gene Expression in Multiple Sclerosis Patients


Nutritional aspects of treatment in epileptic patients


Effects of intermittent fasting on experimental autoimune encephalomyelitis in C57BL/6 mice


Iranian consensus on use of vitamin D in patients with multiple sclerosis


Stem cells: Progressions and applications in clinical medicine


Evaluation of APR1 gene expression in Candida albicans strains isolated from patients with multiple sclerosis


The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population


Report of limb girdle muscular dystrophy type 2a in 6 Iranian patients, one with a novel deletion in CAPN3 gene


Intraspinal delivery of bone marrow stromal cell-derived neural stem cells in patients with amyotrophic lateral sclerosis: A safety and feasibility study


Evaluation of 99mTc-TRODAT-1 SPECT in the diagnosis of Parkinson’s disease versus other progressive movement disorders


Effect of Vitamin A supplementation on fatigue and depression in multiple sclerosis patients: A double-blind placebo-controlled clinical trial


Genetics of GNE myopathy in the non-Jewish Persian population


Mutation in twinkle in a large Iranian family with progressive external ophthalmoplegia, myopathy, dysphagia and dysphonia, and behavior change


Quantitative evaluation of BAFF, HMGB1, TLR 4 and TLR 7 expression in patients with relapsing remitting multiple sclerosis


A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease


Emery-Dreifuss muscular dystrophy: A report of a large family with 11 affected individuals


Memantine for Prophylactic Treatment of Migraine Without Aura: A Randomized Double-Blind Placebo-Controlled Study


Guillain-barré syndrome as first presentation of non-Hodgkin’s lymphoma


Quality of life in medical students with internet addiction


Mitochondrial copy number and D-loop variants in pompe patients


Analysis of copy number variations in patients with autism using cytogenetic and MLPA techniques: Report of 16p13.1p13.3 and 10q26.3 duplications