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Daneshyari Developmental Neuroscience Journas Latest Articles

Developmental Neuroscience Research Articles

Vanishing White Matter Disease With Periodic (Paroxysmal) Hemiparesis
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Cyclic Vomiting With Generalized Epileptiform Discharges Responsive to Topiramate Therapy
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Vagus Nerve Stimulation for Intractable Seizures in Children
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T-Cell Lymphoma Presenting With Neurologic Features in Immunocompetent Children
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Deep Cerebral Venous Thrombosis in an 11-Year-Old Female
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An Infant With a Mitochondrial A3243G Mutation Demonstrating the MELAS Phenotype
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Tuberous Sclerosis With Open Lipped Schizencephaly
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Serum Ferritin in Children With Attention-Deficit Hyperactivity Disorder
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Bilateral Traumatic Carotid Artery Dissection in a Child
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Postictal Psychosis in a Child
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The Incidence of Rett Syndrome in France
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Efficacy and Safety of Zonisamide Monotherapy in a Cohort of Children With Epilepsy
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Orbitofrontal Seizures Presenting With Ictal Visual Hallucinations and Interictal Psychosis
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Increased Intracranial Pressure Due To Chronic Active Epstein-Barr Virus Infection
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Enhanced Capacity of Epilepsy in Brain Malformation Produced During Early Development
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Minor Head Trauma–Induced Sporadic Hemiplegic Migraine Coma
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Impact of Treating Sleep Apnea in a Child With Autism Spectrum Disorder
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Optic Nerve Hypoplasia and Growth Hormone Deficiency in a Cholestatic Infant
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Acute Necrotizing Encephalopathy Associated With Hemophagocytic Syndrome
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Serial Changes on Diffusion-Weighted Magnetic Resonance Imaging in Encephalitis or Encephalopathy
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Myostatin Expression in Muscular Dystrophies and Mitochondrial Encephalomyopathies
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Early Mitochondrial Dysfunction in an Infant With Alexander Disease
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Normal Muscle Respiratory Chain Enzymes Can Complicate Mitochondrial Disease Diagnosis
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Idiopathic Granulomatous Encephalitis Mimicking Malignant Brain Tumor
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Adolescent Pertussis-Induced Partial Arousal Parasomnia
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Transverse Myelitis After Therapy For Primitive Neuroectodermal Tumors
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Neurodegeneration With Brain Iron Accumulation: From Genes to Pathogenesis
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Folinic Acid–Responsive Seizures Initially Responsive to Pyridoxine
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Acute Necrotizing Encephalopathy Associated With Human Herpesvirus-6 Infection
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Neuropathology of Methylmalonic Acidemia in a Child
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Expanding the Clinical Picture of Simpson-Golabi-Behmel Syndrome
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Mirror Movements Following Cortical Resection of Polymicrogyria in a Child With Intractable Epilepsy
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Botulinum Toxin Type A for the Treatment of the Spastic Equinus Foot in Cerebral Palsy
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Landau-Kleffner Syndrome with Mitochondrial Respiratory Chain-Complex I Deficiency
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Myoclonic Seizures in Krabbe Disease: A Unique Presentation in Late-Onset Type
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Fumarate Hydratase Deficiency in Monozygotic Twins
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Cerebral Venous Thrombosis as a First Presentation of Diabetes
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Carbamazepine-Induced Transient Auditory Pitch-Perception Deficit
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A Six-Year Follow-Up MRI Study of Complicated Early Childhood Convulsion
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Emergency Department Admission of Children With Unprovoked Seizure: Recurrence Within 24 Hours
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Subject Index Volume 35
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Moyamoya Syndrome in a Child With Trisomy 12p Syndrome
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Short-Duration ACTH Therapy for Cryptogenic West Syndrome With Better Outcome
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Restless Legs Syndrome Triggered by Heart Surgery
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Pediatric Median Neuropathy Due to Pruritus in Alagille Syndrome
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Nonconvulsive Status Epilepticus and Neurodevelopmental Delay
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CACNA1I Is Not Associated With Childhood Absence Epilepsy in the Chinese Han Population
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Oxcarbazepine Therapy in Very Young Children: A Single-Center Clinical Experience
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Fixation-Off Sensitivity and Generalized Epileptic EEG Induced by Eyes Closed
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Partial Epilepsy Presenting as Apneic Seizures Without Posturing
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Author index (e-only pages)
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Polyneuropathies in teenagers: A clinicopathological study of 45 cases
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Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia
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Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred
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Refsum’s disease may mimic familial Guillain Barre syndrome
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No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy
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Myofibrillar myopathy with congenital cataract and skeletal anomalies without mutations in the desmin, αB-crystallin, myotilin, LMNA or SEPN1 genes
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Outpatient continuous inotrope infusion as an adjunct to heart failure therapy in Duchenne muscular dystrophy
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Dermatomyositis, lobar panniculitis and inflammatory myopathy with abundant macrophages
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Segmental myoclonus as the presenting symptom of an acute disseminated encephalomyelitis: A case report
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Brainstem tuberculoma presenting as eight-and-a-half syndrome
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Colocalization of serotonin and substance P in the postnatal rat trigeminal motor nucleus and its surroundings
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Volume contents (e-only pages)
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A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification
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Breaking Ranks: Space and Number May March to the Beat of a Different Drum
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Losing our Brainless Minds: How Neuroimaging Informs Cognition
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What has Functional Neuroimaging told us about the Mind? So Many Examples, So Little Space
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Mind, Brain, and Functional Neuroimaging
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How Berlusconi Keeps his Face: a Neuropsychological Study in a Case of Semantic Dementia
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Instructions to Authors
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Insulin effects on CSF norepinephrine and cognition in Alzheimer's disease
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Alzheimer's lymphocytes are resistant to ultraviolet B-induced apoptosis
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The Val66Met polymorphism of the brain-derived neurotrophic-factor gene is associated with geriatric depression
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Association study of the vascular endothelial growth factor gene with the risk of developing Alzheimer's disease
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Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease
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BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathy
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Fetal Deformations: A Risk Factor for Obstetrical Brachial Plexus Palsy?
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Hypertension-Induced Cerebellar Encephalopathy and Hydrocephalus in a Male
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Hypomelanosis of Ito Associated With Precocious Puberty
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Focal Glucose Hypermetabolism in Interictal State of West Syndrome
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Congenital Muscular Tortıcollis: Evaluation and Classification
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Subject Index
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Secondary Parkinsonism in Childhood: A Rare Complication After Radiotherapy
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Facial Dysmorphism in Leigh Syndrome With SURF-1 Mutation and COX Deficiency
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Mutation of Gene in Spinal Muscular Atrophy Respiratory Distress Type I
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Lessons from Adult Stroke Trials
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Wheelchair economy class syndrome in amyotrophic lateral sclerosis
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Congenital myopathy with abundant nemaline rods in a cat
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The mouse cerebellum from 1 to 34 months: Parallel fibers
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Juvenile onset acid maltase deficiency presenting as a rigid spine syndrome
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Amyloid myopathy presenting with rhabdomyolysis: Evidence of complement activation
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A case of neuromuscular mimicry
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Muscle slowness in a family with nemaline myopathy
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Keyword Index
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The 5th International Assembly of the World Alliance of Neuromuscular Disorder Associations (WANDA)
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A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset
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A novel sporadic mutation G14739A of the mitochondrial tRNAGlu in a girl with exercise intolerance
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Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2I
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10th Anniversary Congress of the World Muscle Society in Iguaçu, Brazil, September 2005: Reflections
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Predictors of severe chest infections in pediatric neuromuscular disorders
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