Cyclic Vomiting With Generalized Epileptiform Discharges Responsive to Topiramate Therapy Fulltext Access 4 Pages 2006
T-Cell Lymphoma Presenting With Neurologic Features in Immunocompetent Children Fulltext Access 4 Pages 2006
An Infant With a Mitochondrial A3243G Mutation Demonstrating the MELAS Phenotype Fulltext Access 4 Pages 2006
Serum Ferritin in Children With Attention-Deficit Hyperactivity Disorder Fulltext Access 4 Pages 2006
Efficacy and Safety of Zonisamide Monotherapy in a Cohort of Children With Epilepsy Fulltext Access 4 Pages 2006
Orbitofrontal Seizures Presenting With Ictal Visual Hallucinations and Interictal Psychosis Fulltext Access 4 Pages 2006
Increased Intracranial Pressure Due To Chronic Active Epstein-Barr Virus Infection Fulltext Access 4 Pages 2006
Enhanced Capacity of Epilepsy in Brain Malformation Produced During Early Development Fulltext Access 4 Pages 2006
Optic Nerve Hypoplasia and Growth Hormone Deficiency in a Cholestatic Infant Fulltext Access 4 Pages 2006
Acute Necrotizing Encephalopathy Associated With Hemophagocytic Syndrome Fulltext Access 4 Pages 2006
Serial Changes on Diffusion-Weighted Magnetic Resonance Imaging in Encephalitis or Encephalopathy Fulltext Access 4 Pages 2006
Myostatin Expression in Muscular Dystrophies and Mitochondrial Encephalomyopathies Fulltext Access 4 Pages 2006
Normal Muscle Respiratory Chain Enzymes Can Complicate Mitochondrial Disease Diagnosis Fulltext Access 4 Pages 2006
Neurodegeneration With Brain Iron Accumulation: From Genes to Pathogenesis Fulltext Access 4 Pages 2006
Acute Necrotizing Encephalopathy Associated With Human Herpesvirus-6 Infection Fulltext Access 4 Pages 2006
Mirror Movements Following Cortical Resection of Polymicrogyria in a Child With Intractable Epilepsy Fulltext Access 4 Pages 2006
Botulinum Toxin Type A for the Treatment of the Spastic Equinus Foot in Cerebral Palsy Fulltext Access 4 Pages 2006
Landau-Kleffner Syndrome with Mitochondrial Respiratory Chain-Complex I Deficiency Fulltext Access 4 Pages 2006
Myoclonic Seizures in Krabbe Disease: A Unique Presentation in Late-Onset Type Fulltext Access 4 Pages 2006
A Six-Year Follow-Up MRI Study of Complicated Early Childhood Convulsion Fulltext Access 4 Pages 2006
Emergency Department Admission of Children With Unprovoked Seizure: Recurrence Within 24 Hours Fulltext Access 4 Pages 2006
Short-Duration ACTH Therapy for Cryptogenic West Syndrome With Better Outcome Fulltext Access 4 Pages 2006
CACNA1I Is Not Associated With Childhood Absence Epilepsy in the Chinese Han Population Fulltext Access 4 Pages 2006
Oxcarbazepine Therapy in Very Young Children: A Single-Center Clinical Experience Fulltext Access 4 Pages 2006
Fixation-Off Sensitivity and Generalized Epileptic EEG Induced by Eyes Closed Fulltext Access 4 Pages 2006
Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia Fulltext Access 4 Pages 2006
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred Fulltext Access 4 Pages 2006
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy Fulltext Access 4 Pages 2006
Myofibrillar myopathy with congenital cataract and skeletal anomalies without mutations in the desmin, αB-crystallin, myotilin, LMNA or SEPN1 genes Fulltext Access 4 Pages 2006
Outpatient continuous inotrope infusion as an adjunct to heart failure therapy in Duchenne muscular dystrophy Fulltext Access 4 Pages 2006
Dermatomyositis, lobar panniculitis and inflammatory myopathy with abundant macrophages Fulltext Access 4 Pages 2006
Segmental myoclonus as the presenting symptom of an acute disseminated encephalomyelitis: A case report Fulltext Access 4 Pages 2006
Colocalization of serotonin and substance P in the postnatal rat trigeminal motor nucleus and its surroundings Fulltext Access 4 Pages 2006
A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification Fulltext Access 4 Pages 2006
Breaking Ranks: Space and Number May March to the Beat of a Different Drum Fulltext Access 4 Pages 2006
What has Functional Neuroimaging told us about the Mind? So Many Examples, So Little Space Fulltext Access 4 Pages 2006
How Berlusconi Keeps his Face: a Neuropsychological Study in a Case of Semantic Dementia Fulltext Access 4 Pages 2006
Insulin effects on CSF norepinephrine and cognition in Alzheimer's disease Fulltext Access 4 Pages 2006
Alzheimer's lymphocytes are resistant to ultraviolet B-induced apoptosis Fulltext Access 4 Pages 2006
The Val66Met polymorphism of the brain-derived neurotrophic-factor gene is associated with geriatric depression Fulltext Access 4 Pages 2006
Association study of the vascular endothelial growth factor gene with the risk of developing Alzheimer's disease Fulltext Access 4 Pages 2006
Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease Fulltext Access 4 Pages 2006
BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathy Fulltext Access 4 Pages 2006
Fetal Deformations: A Risk Factor for Obstetrical Brachial Plexus Palsy? Fulltext Access 4 Pages 2006
Hypertension-Induced Cerebellar Encephalopathy and Hydrocephalus in a Male Fulltext Access 4 Pages 2006
Secondary Parkinsonism in Childhood: A Rare Complication After Radiotherapy Fulltext Access 4 Pages 2006
Facial Dysmorphism in Leigh Syndrome With SURF-1 Mutation and COX Deficiency Fulltext Access 4 Pages 2006
Juvenile onset acid maltase deficiency presenting as a rigid spine syndrome Fulltext Access 4 Pages 2006
Amyloid myopathy presenting with rhabdomyolysis: Evidence of complement activation Fulltext Access 4 Pages 2006
The 5th International Assembly of the World Alliance of Neuromuscular Disorder Associations (WANDA) Fulltext Access 4 Pages 2006
A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset Fulltext Access 4 Pages 2006
A novel sporadic mutation G14739A of the mitochondrial tRNAGlu in a girl with exercise intolerance Fulltext Access 4 Pages 2006
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2I Fulltext Access 4 Pages 2006
10th Anniversary Congress of the World Muscle Society in Iguaçu, Brazil, September 2005: Reflections Fulltext Access 4 Pages 2006
Predictors of severe chest infections in pediatric neuromuscular disorders Fulltext Access 4 Pages 2006