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Daneshyari Developmental Neuroscience Journas Latest Articles

Developmental Neuroscience Research Articles

Impaired glycemia increases disease progression in mild cognitive impairment
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Clinical features of Japanese patients with inclusion body myositis
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Post-mortem 7.0-tesla magnetic resonance study of cortical microinfarcts in neurodegenerative diseases and vascular dementia with neuropathological correlates
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Profile of memory impairment as a prognostic marker in amnestic mild cognitive impairment
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Extrathymic malignancies in a defined cohort of patients with myasthenia gravis
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3-week whole body vibration does not improve gait function in mildly affected multiple sclerosis patients-a randomized controlled trial
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Increased proinflammatory cytokines in sera of patients with multifocal motor neuropathy
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Meta-analysis of the association between two neprilysin gene polymorphisms and Alzheimer's disease
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A novel treatment target for Parkinson's disease
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Implicit learning is better at subjectively defined non-optimal time of day
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Validation of next-generation sequencing technologies in genetic diagnosis of dementia
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Dietary and lifestyle guidelines for the prevention of Alzheimer's disease
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Markers of endothelial dysfunction and cerebral blood flow in older adults
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Early infarct growth predicts long-term clinical outcome in ischemic stroke
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Detecting gene mutations in Japanese Alzheimer's patients by semiconductor sequencing
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Subjective cognitive decline predicts future deterioration in cognitively normal patients with Parkinson's disease
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Relationships between macular pigment optical density and cognitive function in unimpaired and mildly cognitively impaired older adults
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Cross-region reduction in 5-hydroxymethylcytosine in Alzheimer's disease brain
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Bexarotene reduces network excitability in models of Alzheimer's disease and epilepsy
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Granulomatous Herpes Simplex Encephalitis in an Infant With Multicystic Encephalopathy: A Distinct Clinicopathologic Entity?
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Pontine Malformation, Undecussated Pyramidal Tracts, and Regional Polymicrogyria: A New Syndrome
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Increased Association Between Febrile Convulsion and Allergic Rhinitis in Children: A Nationwide Population-Based Retrospective Cohort Study
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Spectrum of Visual Disorders in a Population-Based Cerebral Palsy Cohort
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Intraoperative Electroencephalography Predicts Postoperative Seizures in Infants With Congenital Heart Disease
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Original ArticleRisk of Subsequent Asthma in Children With Febrile Seizures: A Nationwide Population-Based Retrospective Cohort Study
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Voluntary control of facial musculature in Parkinson's disease
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Accuracy of osmophobia in the differential diagnosis between migraine and tension-type headache
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Etiological mechanisms of isolated pontine infarcts based on arterial territory involvement
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A case of Parry-Romberg syndrome and alien hand
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Circulating levels of adipokines in Parkinson's disease
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Acute-onset chronic inflammatory demyelinating polyneuropathy with focal segmental glomerulosclerosis
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Risk factors for mental disorders in patients with hypertensive intracerebral hemorrhage following neurosurgical treatment
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Reliability of transcranial magnetic stimulation induced corticomotor excitability measurements for a hand muscle in healthy and chronic stroke subjects
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Altered spontaneous activity in treatment-naive childhood absence epilepsy revealed by Regional Homogeneity
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A novel ferritin light chain mutation in neuroferritinopathy with an atypical presentation
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Features of anti-aquaporin 4 antibody-seronegative Thai patients with neuromyelitis optica spectrum disorders: A comparison with seropositive cases
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Cognitive dysfunction in patients with multiple sclerosis treated with different types of interferon beta: A randomized clinical trial
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Mutational screening of 320 Brazilian patients with autosomal dominant spinocerebellar ataxia
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Clinical ObservationsCase Study for the Evaluation of Current Treatment Recommendations of Guanidinoacetate Methyltransferase Deficiency: Ineffectiveness of Sodium Benzoate
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Non-invasive brain stimulation of the right inferior frontal gyrus may improve attention in early Alzheimer's disease: A pilot study
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Central retinal artery occlusion with concomitant ipsilateral cerebral infarction after cosmetic facial injections
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Diagnosis of cystathionine beta-synthase deficiency by genetic analysis
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Clinical and demographic predictors of mild cognitive impairment for converting to Alzheimer's disease and reverting to normal cognition
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Brain metabolites in autonomic regulatory insular sites in heart failure
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The relationship of leukoaraiosis and the clinical severity of vascular Parkinsonism
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Usefulness of sacral nerve modulation in a series of multiple sclerosis patients with bladder dysfunction
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Information processing speed impairment and cerebellar dysfunction in relapsing-remitting multiple sclerosis
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Parasomnias and isolated sleep symptoms in Parkinson's disease: A questionnaire study on 661 patients
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Predictors of development of chronic vestibular insufficiency after vestibular neuritis
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Impact of tetrabenazine on gait and functional mobility in individuals with Huntington's disease
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A case of adult-onset reducing body myopathy presenting a novel clinical feature, asymmetrical involvement of the sternocleidomastoid and trapezius muscles
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Guide for Authors
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Subject Index to Volume 36
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Announcements and reports
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Serum and cerebrospinal fluid levels of visinin-like protein-1 in acute encephalopathy with biphasic seizures and late reduced diffusion
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Cognitive performance and convulsion risk after experimentally-induced febrile-seizures in rat
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In vivo evaluation of optic nerve development in non-human primates by using diffusion tensor imaging
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Diagnosing young children with autism
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Síndrome de cascanueces: causa de hematuria y proteinuria masiva no glomerular
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Huntingtin is associated with cytomatrix proteins at the presynaptic terminal
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Reduced spontaneous sympathetic nerve activity in multiple sclerosis patients
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Global brain atrophy but not hippocampal atrophy is related to type 2 diabetes
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Novel genetic variants modify the effect of smoking on carotid plaque burden in Hispanics
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Delayed myelination is not a constant feature of Allan–Herndon–Dudley syndrome: Report of a new case and review of the literature
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Paraneoplastic downbeat nystagmus associated with cerebellar hypermetabolism especially in the nodulus
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Clinical features and disability progression in multiple sclerosis in Tunisia: Do we really have a more aggressive disease course?
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Gray matter volume in relation to cardio-vascular stiffness
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Brainstem and spinal reflex studies in patients with primary progressive freezing of gait
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Clinical characteristics of Parkinson's disease patients in Greece: A multicenter, nation-wide, cross-sectional study
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The safety of exercise training in multiple sclerosis: A systematic review
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Polymyositis in solid organ transplant recipients receiving tacrolimus
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Clinical features and neuropsychological profile in vascular parkinsonism
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Novel characterization of gait impairments in people with multiple sclerosis by means of the gait profile score
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Identification and characterization of a novel splice-site mutation in the Wilson disease gene
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Freezing of gait in Chinese patients with Parkinson Disease
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Characterization of early onset neurofibromatosis type 2
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Rituximab Use in Pediatric Central Demyelinating Disease
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Therapeutic Hypothermia in Neonates and Selective Hippocampal Injury on Diffusion-Weighted Magnetic Resonance Imaging
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Cross-sectional Evaluation of Electrical Impedance Myography and Quantitative Ultrasound for the Assessment of Duchenne Muscular Dystrophy in a Clinical Trial Setting
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Polyols accumulated in ribose-5-phosphate isomerase deficiency increase mitochondrial superoxide production and improve antioxidant defenses in rats' prefrontal cortex
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Fraternal Twins With Autism, Severe Cognitive Deficit, and Epilepsy: Diagnostic Role of Chromosomal Microarray Analysis
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Ataxia, Ophthalmoplegia, and Impairment of Consciousness in a 19-Month-Old American Boy
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Case of a Two-Year-Old Boy With Recurrent Seizures, Abnormal Movements, and Central Hypoventilation
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Temporoparietal Resection in a Patient With Landau-Kleffner Syndrome
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An Unusual Cause of Peroneal Neuropathy
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A 7-Year-Old Girl With Hypertrophic Cardiomyopathy and Progressive Scoliosis
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The Ketogenic Diet: Initiation at Goal Calories Versus Gradual Caloric Advancement
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Histological, biochemical, and genetic characterization of early-onset fulminating sialidosis type 2 in a Korean neonate with hydrops fetalis
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Hematoma volume as the major determinant of outcomes after intracerebral hemorrhage
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Effect of a blackout in pediatric patients with home medical devices during the 2011 eastern Japan earthquake
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Announcements and reports
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Natural evolution from idiopathic photosensitive occipital lobe epilepsy to idiopathic generalized epilepsy in an untreated young patient
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Effects of clonazepam on self-induced photoparoxysmal responses
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Announcements and reports
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The ominous sequence in patients with tuberous sclerosis complex
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Announcements and reports
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Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy
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Announcements and reports
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Williams–Beuren syndrome with brain malformation and hypertrophic cardiomyopathy
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Carnitine palmitoyltransferase 2 gene polymorphism is a genetic risk factor for sudden unexpected death in infancy
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