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Lancet Neurology, The, ISSN 1474-4422, 2008, Volume 7, Issue 12, pp. 1091 - 1098
Summary Background A severe form of encephalitis associated with antibodies against NR1–NR2 heteromers of the NMDA receptor was recently identified. We aimed... 
Neurology | IMMUNITY | OVARIAN TERATOMA | AUTOIMMUNITY | DYSKINESIA | DISEASE | DISORDERS | SYNAPTIC PLASTICITY | MIDAZOLAM | VIRUSES | CLINICAL NEUROLOGY | KETAMINE | Neurocognitive Disorders - immunology | Encephalitis - diagnosis | Protein Subunits - immunology | Teratoma - physiopathology | Humans | Middle Aged | Ovarian Neoplasms - physiopathology | Paraneoplastic Syndromes, Nervous System - immunology | Child, Preschool | Male | Epilepsy - physiopathology | Epitopes - immunology | Young Adult | Autoimmune Diseases of the Nervous System - physiopathology | Encephalitis - physiopathology | Epilepsy - immunology | Adult | Female | Child | Receptors, N-Methyl-D-Aspartate - immunology | Autoimmune Diseases of the Nervous System - diagnosis | Cell Line | Paraneoplastic Syndromes, Nervous System - physiopathology | Brain - physiopathology | Cells, Cultured | Neurocognitive Disorders - physiopathology | Rats | Teratoma - immunology | Encephalitis - immunology | Autoimmune Diseases of the Nervous System - immunology | Autoantibodies - immunology | Animals | Autoantigens - immunology | Adolescent | Aged | Brain - immunology | Ovarian Neoplasms - immunology | Viral antibodies | Antibodies | Methyl aspartate | Encephalitis | Neurosciences | Analysis | Index Medicus | Cell culture | Translation | Glutamic acid receptors (ionotropic) | Memory | N-Methyl-D-aspartic acid receptors | Glutamic acid receptors | Epitopes | Hospitals | Hypoventilation | Autonomic nervous system | Immunotherapy | Dendrites | Children | teratoma | Age | Enzyme-linked immunosorbent assay | Dyskinesia | Seizures | Tumors
Journal Article
Journal Article
Epilepsia, ISSN 0013-9580, 01/2015, Volume 56, Issue 1, pp. e1 - e5
Journal Article
1995, Advances in neurology, ISBN 9780781702645, Volume 67., xv, 398
Book
Journal Article
Human Brain Mapping, ISSN 1065-9471, 10/2007, Volume 28, Issue 10, pp. 1023 - 1032
Journal Article
Experimental Neurology, ISSN 0014-4886, 2008, Volume 213, Issue 1, pp. 71 - 83
Patients with temporal lobe epilepsy are frequently afflicted with psychiatric comorbidity and deficits in spatial and other forms of declarative memory. The... 
Learning and memory | Hippocampal sclerosis | Depression | Anxiety | Psychopathology | Glutamate | Seizures | WATER-MAZE | hippocampal sclerosis | PSYCHIATRIC COMORBIDITY | KAINIC ACID | GRANULE CELL DISPERSION | NEUROSCIENCES | anxiety | ANTIDEPRESSANT ACTIVITY | learning and memory | psychopathology | PILOCARPINE MODEL | seizures | RAT HIPPOCAMPUS | depression | INDUCED STATUS EPILEPTICUS | SPONTANEOUS RECURRENT SEIZURES | glutamate | Epilepsy, Temporal Lobe - psychology | Memory Disorders - physiopathology | Nerve Degeneration - physiopathology | Status Epilepticus - chemically induced | Epilepsy, Temporal Lobe - physiopathology | Learning Disorders - physiopathology | Hippocampus - drug effects | Dentate Gyrus - physiopathology | Nerve Degeneration - chemically induced | Dentate Gyrus - drug effects | Female | Depressive Disorder - chemically induced | Disease Models, Animal | Mood Disorders - chemically induced | Mental Disorders - chemically induced | Epilepsy, Temporal Lobe - chemically induced | Kainic Acid - pharmacology | Status Epilepticus - pathology | Neurocognitive Disorders - physiopathology | Excitatory Amino Acid Agonists - pharmacology | Hippocampus - pathology | Neurocognitive Disorders - chemically induced | Maze Learning - drug effects | Nerve Degeneration - pathology | Mental Disorders - physiopathology | Neuropsychological Tests | Learning Disorders - chemically induced | Animals | Depressive Disorder - physiopathology | Status Epilepticus - physiopathology | Convulsants - pharmacology | Mice | Mood Disorders - physiopathology | Dentate Gyrus - pathology | Hippocampus - physiopathology | Memory Disorders - chemically induced | Temporal lobe epilepsy | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 11/2010, Volume 468, Issue 7321, pp. 263 - 269
Mutations in the X-linked MECP2 gene, which encodes the transcriptional regulator methyl-CpG-binding protein 2 (MeCP2), cause Rett syndrome and several... 
GLUTAMIC-ACID DECARBOXYLASE | GENE | 67 KDA | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | MUTATION | NEURONAL MECP2 | SCHIZOPHRENIA | MICE | CPG-BINDING PROTEIN-2 | YOUNG GIRLS | Autistic Disorder - physiopathology | gamma-Aminobutyric Acid - metabolism | Methyl-CpG-Binding Protein 2 - metabolism | Male | Psychomotor Disorders - complications | Methyl-CpG-Binding Protein 2 - deficiency | Compulsive Behavior - physiopathology | Neurons - metabolism | Disease Models, Animal | Autistic Disorder - genetics | Signal Transduction | Compulsive Behavior - genetics | Genotype | Mice, Transgenic | Survival Rate | Hippocampus - pathology | Rett Syndrome - physiopathology | Self-Injurious Behavior - genetics | Phenotype | Neuronal Plasticity | Long-Term Potentiation | Stereotypic Movement Disorder - genetics | Compulsive Behavior - complications | Glutamate Decarboxylase - metabolism | Mice | Hippocampus - physiopathology | Autistic Disorder - pathology | Rett Syndrome - complications | Neural Inhibition | Stereotypic Movement Disorder - pathology | Reflex, Startle - genetics | Electroencephalography | Methyl-CpG-Binding Protein 2 - genetics | Synaptic Transmission | Psychomotor Disorders - genetics | Self-Injurious Behavior - complications | Psychomotor Disorders - physiopathology | Inhibitory Postsynaptic Potentials | Stereotypic Movement Disorder - physiopathology | Brain - cytology | Homeodomain Proteins - genetics | Stereotypic Movement Disorder - complications | Self-Injurious Behavior - physiopathology | Animals | Rett Syndrome - pathology | Vesicular Inhibitory Amino Acid Transport Proteins - genetics | Presynaptic Terminals - metabolism | Autistic Disorder - complications | Respiration | Rett Syndrome - genetics | Autism | Care and treatment | Rett syndrome | Schizophrenia | GABA | Genetic aspects | Diagnosis | Cognition disorders | Seizures (Medicine) | Health aspects | Studies | Anxieties | Social interaction | Neurons | Rodents | Bipolar disorder | Behavior | Gene expression | Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 07/2007, Volume 69, Issue 5, pp. 434 - 441
Objective: Ictal asystole (IA) is a rare event mostly seen in patients with temporal lobe epilepsy (TLE) and a potential contributor to sudden unexplained... 
CARDIAC ASYSTOLE | ARRHYTHMIAS | TEMPORAL-LOBE EPILEPSY | BRADYCARDIA SYNDROME | SUDDEN-DEATH | SYNCOPE | DROP ATTACKS | PARTIAL SEIZURES | INSULAR CORTEX STIMULATION | ECG-CHANGES | CLINICAL NEUROLOGY | Predictive Value of Tests | Electroencephalography - standards | Brain - anatomy & histology | Monitoring, Physiologic - standards | Syncope - diagnosis | Bradycardia - diagnosis | Humans | Middle Aged | Child, Preschool | Death, Sudden, Cardiac - prevention & control | Epilepsy, Temporal Lobe - physiopathology | Male | Death, Sudden, Cardiac - etiology | Epilepsy - physiopathology | Epilepsy, Temporal Lobe - complications | Epilepsy, Temporal Lobe - diagnosis | Adult | Female | Electroencephalography - trends | Epilepsy, Generalized - etiology | Autonomic Pathways - physiopathology | Video Recording - standards | Brain - physiopathology | Bradycardia - physiopathology | Brain Ischemia - physiopathology | Brain Ischemia - etiology | Heart Arrest - physiopathology | Electrodiagnosis - methods | Electroencephalography - methods | Heart Arrest - diagnosis | Epilepsy - complications | Epilepsy - diagnosis | Epilepsy, Generalized - physiopathology | Syncope - physiopathology | Electrodiagnosis - standards | Video Recording - trends | Bradycardia - etiology | Video Recording - methods | Adolescent | Electrodiagnosis - trends | Syncope - etiology | Brain Ischemia - diagnosis | Heart Arrest - etiology | Monitoring, Physiologic - methods | Monitoring, Physiologic - instrumentation | Aged | Early Diagnosis | Index Medicus | Abridged Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 12/2008, Volume 71, Issue 24, pp. 1981 - 1985
Journal Article
Epilepsia, ISSN 0013-9580, 11/2011, Volume 52, Issue 11, pp. 1949 - 1955
Purpose:  Febrile seizures (FS) are the most common type of convulsive events in children. FS are suggested to result from a combination of genetic and... 
Febrile seizure | Triggering mechanism | Respiration | Alkalosis | RECTAL DIAZEPAM | ACIDOSIS | CONVULSIONS | MODEL | CLINICAL NEUROLOGY | EMERGENCY TREATMENT | INCREASE | EPILEPSY | CARBON-DIOXIDE | MIDAZOLAM | Tonsillitis - physiopathology | Humans | Urinary Tract Infections - physiopathology | Child, Preschool | Infant | Male | Urinary Tract Infections - complications | Fever - physiopathology | Otitis Media - physiopathology | Seizures, Febrile - physiopathology | Female | Chickenpox - complications | Fever of Unknown Origin - physiopathology | Emergency Service, Hospital | Scarlet Fever - physiopathology | Tonsillitis - complications | Alkalosis, Respiratory - physiopathology | Alkalosis, Respiratory - complications | Acid-Base Equilibrium - physiology | Scarlet Fever - complications | Seizures, Febrile - etiology | Fever of Unknown Origin - complications | Chickenpox - physiopathology | Otitis Media - complications | Gastroenteritis - physiopathology | Neurosciences | Analysis | Gastroenteritis | Medical care | Respiratory tract diseases | Development and progression | Urinary tract infections | Febrile convulsions | Disease susceptibility | Universities and colleges | Quality management | Index Medicus | Brain | Animal models | Scarlet fever | Urinary tract | pH effects | Blood | Fever | Infection | Tonsillitis | Hospitals | Etiology | Otitis media | Children | Acid-base status | Acidosis | Seizures
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2006, Volume 244, Issue 1, pp. 117 - 122
Paucity of studies on neurological manifestations in dengue virus infection prompted this study. We aim to correlate clinical, radiological and... 
MRI | Dengue | Encephalopathy | EEG | Outcome | Myositis | EMG | myositis | JAPANESE ENCEPHALITIS | dengue | encephalopathy | NEUROSCIENCES | outcome | CLINICAL NEUROLOGY | FEVER | Myoclonus - virology | Prospective Studies | Encephalitis, Viral - virology | Myoclonus - diagnosis | Muscle Weakness - diagnosis | Humans | Middle Aged | Central Nervous System - pathology | Child, Preschool | Male | Seizures - virology | Electroencephalography | Myositis - complications | Leukocytosis - virology | Encephalitis, Viral - diagnosis | Muscle Weakness - virology | Seizures - physiopathology | Brain Diseases, Metabolic - diagnosis | Spinal Cord - pathology | Leukocytosis - physiopathology | Adult | Female | Globus Pallidus - physiopathology | Child | Globus Pallidus - pathology | Central Nervous System - virology | Globus Pallidus - virology | Creatine Kinase - blood | Encephalitis, Viral - physiopathology | Brain Diseases, Metabolic - virology | Leukocytosis - diagnosis | Seizures - diagnosis | Myoclonus - physiopathology | Magnetic Resonance Imaging | Dengue - complications | Myositis - virology | Brain Diseases, Metabolic - physiopathology | Adolescent | Aged | Spinal Cord - physiopathology | Central Nervous System - physiopathology | Muscle Weakness - physiopathology | Spinal Cord - virology | Myositis - physiopathology | Health aspects | Index Medicus
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 2016, Volume 59, Issue 11, pp. 577 - 583
Abstract Raine syndrome is a rare autosomal recessive bone dysplasia characterized by characteristic facial features with exophthalmos and generalized... 
Medical Education | Raine syndrome | FAM20C gene | Kohlschutter-Tonz syndrome | OSTEOSCLEROTIC BONE DYSPLASIA | DENTINOGENESIS | GENETICS & HEREDITY | FAM20C | MUTATIONS | AMELOGENESIS | Cleft Palate - diagnosis | Microcephaly - genetics | Seizures - genetics | Bone Diseases, Developmental - mortality | Casein Kinase I - genetics | Humans | Dementia - diagnosis | Dementia - physiopathology | Learning Disorders - physiopathology | Male | Cleft Palate - genetics | Epilepsy - mortality | Microcephaly - mortality | Abnormalities, Multiple - mortality | Amelogenesis Imperfecta - genetics | Bone Diseases, Developmental - genetics | Epilepsy - physiopathology | Exophthalmos - mortality | Dementia - genetics | Bone Diseases, Developmental - physiopathology | Osteosclerosis - mortality | Seizures - physiopathology | Amelogenesis Imperfecta - diagnosis | Exophthalmos - genetics | Amelogenesis Imperfecta - mortality | Epilepsy - genetics | Female | Microcephaly - physiopathology | Osteosclerosis - genetics | Abnormalities, Multiple - genetics | Diagnosis, Differential | Cleft Palate - mortality | Osteosclerosis - diagnosis | Amelogenesis Imperfecta - physiopathology | Extracellular Matrix Proteins - genetics | Microcephaly - diagnosis | Exophthalmos - physiopathology | Cleft Palate - physiopathology | Abnormalities, Multiple - physiopathology | Exophthalmos - diagnosis | Dementia - mortality | Epilepsy - diagnosis | Phenotype | Abnormalities, Multiple - diagnosis | Adolescent | Learning Disorders - genetics | Osteosclerosis - physiopathology | Biodegradation | Dysplasia | Learning disabilities | Diagnosis | Seizures (Medicine) | Casein | Index Medicus
Journal Article