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Daneshyari Neurology Journas Latest Articles

Neurology Research Articles

Netrin G1 Mutations Are an Uncommon Cause of Atypical Rett Syndrome With or Without Epilepsy
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Ictal EEG in Benign Partial Epilepsy in Infancy
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Effects of Febrile and Afebrile Seizures on Oxidant State in Children
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Suspected Herpes Encephalitis and Opercular Syndrome in Childhood
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Magnetoencephalographic Findings of Panayiotopoulos Syndrome With Frontal Epileptic Discharges
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Altered Nestin Expression in the Cerebrum With Periventricular Leukomalacia
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Increased Prevalence of Silent Celiac Disease Among Greek Epileptic Children
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Benign Epilepsy of Childhood With Rolandic Spikes: Typical and Atypical Variants
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PHACE Syndrome with Intracerebral Hemangiomas, Heterotopia, and Endocrine Dysfunction
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ARSA Gene Mutations in Five Chinese Metachromatic Leukodystrophy Patients
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Infantile Onset of Hereditary Spastic Paraplegia Poorly Predicts the Genotype
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Elevation of Tumor Necrosis Factor-Alpha in Cerebrospinal Fluid of Autistic Children
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Effects of Heavy In Utero Cocaine Exposure on Adolescent Caudate Morphology
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Selenium and Intractable Epilepsy: Is There Any Correlation?
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Bone Mineral Density With Lamotrigine Monotherapy for Epilepsy
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Association of Cerebral Palsy With Other Disabilities in Children With Perinatal Arterial Ischemic Stroke
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Evolution of Subclinical Hypothyroidism in Children Treated With Antiepileptic Drugs
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Neurofibromatosis: Novel and Recurrent Mutations in Turkish Patients
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Age-Related Variation in Presenting Signs of Childhood Arterial Ischemic Stroke
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Apneic Seizures: A Sign of Temporal Lobe Hemorrhage in Full-Term Neonates
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Oxcarbazepine in Children With Nocturnal Frontal-Lobe Epilepsy
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Index mots cles
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Aspects cliniques et électrophysiologiques de l’intoxication aiguë aux organophosphorés
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Respiratory-related evoked potentials in children with asthma
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High erythropoietin and low vascular endothelial growth factor levels in cerebrospinal fluid from hypoxemic ALS patients suggest an abnormal response to hypoxia
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Recent developments in the management of peripheral neuropathy using skin biopsy
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The effects of brain tissue decomposition on diffusion tensor imaging and tractography
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Heritability of anterior cingulate response to conflict: An fMRI study in female twins
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CommentaryA BOLD search for baseline
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Role of Cytogenetics and Molecular Cytogenetics in the Diagnosis of Genetic Imbalances
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Bone Consequences of Epilepsy and Antiepileptic Medications
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Epilepsy in Hypothalamic Hamartoma: Clinical and EEG Features
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Où en sont les études génétiques de la SEP ?
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Promouvoir la remyélinisation dans le cadre de la sclérose en plaque à l'aide des cellules neurales/précurseurs et/ou souches endogènes adultes
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Experimental models of multiple sclerosis
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Les fluctuations non motrices de la maladie de Parkinson
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Œdème cérébral vasogénique par syndrome de reperfusion post-endartérectomie carotidienne
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Prise en charge des accidents vasculaires cérébraux au Sénégal
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Quantitative analysis of CAPN3 transcripts in LGMD2A patients: Involvement of nonsense-mediated mRNA decay
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Activité électromyographique neurogène dans un cas de syndrome de Lambert-Eaton non-paranéoplasique
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Sclérose en plaques : immunomodulateurs, éducation et auto-injection
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Polyradiculonévrite chronique et sarcoïdose : association fortuite
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Aspects épidémiologiques et cliniques des polyradiculonévrites chroniques
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The Impact of Pelizaeus-Merzbacher Disease on the Family
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Childhood Status Epilepticus and Excitotoxic Neuronal Injury
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Semiological Seizure Classification: Before and After Video-EEG Monitoring of Seizures
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MRI Findings in Pediatric Ophthalmoplegic Migraine: A Case Report and Literature Review
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Caffeine as an Adjuvant to Ibuprofen in Treating Childhood Headaches
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Prognosis and Predictive Factors of Partial Seizures in Children
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Association of GABRG2 Polymorphisms With Idiopathic Generalized Epilepsy
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Arachnoiditis ossificans with progressive syringomyelia and spinal arachnoid cyst
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CTLA4 gene polymorphisms and multiple sclerosis in Northern Ireland
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No effect of APOE and PVRL2 on the clinical outcome of multiple sclerosis
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Proteome analysis of cerebrospinal fluid in Guillain–Barré syndrome (GBS)
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IgG subclass distribution of autoantibodies in pediatric opsoclonus–myoclonus syndrome
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High production of RANTES and MIP-1α in the tropical spastic paraparesis/HTLV-1-associated myelopathy (TSP/HAM)
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Origin of ganglioside complex antibodies in Guillain–Barré syndrome
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GABA (A) receptor subunits RNA expression in mice peritoneal macrophages modulate their IL-6/IL-12 production
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Lewis rats immunized with GM1 ganglioside do not develop peripheral neuropathy
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Anti-GQ1b antibody does not affect neuromuscular transmission in human limb muscle
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FcRL3 and multiple sclerosis pathogenesis: Role in autoimmunity?
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Immunohistochemical and ultrastructural abnormalities in muscle from a patient with sensorineural hearing loss related to a 1555 A-to-G mitochondrial mutation
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Reactivation of dormant lumbar methicillin-resistant Staphylococcus aureus osteomyelitis after 12 years
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Involvement of the SgIGSF/Necl-2 adhesion molecule in degranulation of mesenteric mast cells
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Evaluation of white matter structures in patients with tinnitus using diffusion tensor imaging
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Sporadic encephalitis lethargica
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Osmotic demyelination syndromes: Central and extrapontine myelinolysis
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Congenital disorder of glycosylation type 1a: Three siblings with a mild neurological phenotype
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Dysphagia in acute ischaemic stroke: severity, recovery and relationship to stroke subtype
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Pharmacoeconomics of therapy for Guillain–Barré syndrome: plasma exchange and intravenous immunoglobulin
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Transventricular hemispherotomy for surgical treatment of intractable epilepsy
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Temporary alopecia after subarachnoid haemorrhage
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Progressive ataxic gait disorder
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History of neurosciences at the School of Medical Sciences, Universiti Sains Malaysia
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Hollow bone cement filled with impacted cancellous bone as a substitute for bone grafts in cervical spine fusion
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Cytoarchitecture of the cerebral cortex—More than localization
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Hand versus mouth for call–bell activation by DMD and Becker patients
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Dystrophin-dependent muscle degeneration requires a fully functional contractile machinery to occur in C. elegans
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The Dutch neuromuscular database CRAMP (Computer Registry of All Myopathies and Polyneuropathies): Development and preliminary data
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MRI in DNM2-related centronuclear myopathy: Evidence for highly selective muscle involvement
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Inherited neuromyotonia: A clinical and genetic study of a family
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Commentary from the Editor
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Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation
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Dysferlinopathy in the Jews of the Caucasus: A frequent mutation in the dysferlin gene
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144th ENMC International Workshop: Outcome Measures in McArdle Disease, 29 September-1 November 2006, Naarden, The Netherlands
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Paraneoplastic myopathy: response to intravenous immunoglobulin
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An expanded version of the Hammersmith Functional Motor Scale for SMA II and III patients
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Low-resolution electromagnetic brain tomography (LORETA) of monozygotic twins discordant for chronic fatigue syndrome
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Usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy
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On navigating the human cerebral cortex: Response to ‘in praise of tedious anatomy’
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What is where and why it is important
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Specific increase of human entorhinal population synaptic and neuronal activity during retrieval
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The urokinase-type plasminogen activator polymorphism PLAU_1 is a risk factor for APOE-ε4 non-carriers in the Italian Alzheimer’s disease population and does not affect the plasma Aβ(1–42) level
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Subject index of volume 182
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Subject index of volume 183
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Specific antibody index in cerebrospinal fluid from patients with central and peripheral paraneoplastic neurological syndromes
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Antigen therapy of experimental autoimmune encephalomyelitis selectively induces apoptosis of pathogenic T cells
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Identification of interferon-beta antibodies in a reference laboratory setting: Findings for 1144 consecutive sera
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The IgG subclass-specificities of anti-IFNβ antibodies change with time and differ between the IFNβ products in relapsing remitting multiple sclerosis patients
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Helicobacter pylori infection is a potential protective factor against conventional multiple sclerosis in the Japanese population
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