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Lancet neurology, 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 | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | 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 (Copenhagen), ISSN 0013-9580, 01/2015, Volume 56, Issue 1, pp. e1 - e5
Journal Article
Journal of neurology, ISSN 0340-5354, 3/2010, Volume 257, Issue 3, pp. 466 - 468
Journal Article
Nature (London), ISSN 1476-4687, 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... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | 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
Current Opinion in Pharmacology, ISSN 1471-4892, 2014, Volume 20, pp. 83 - 88
Journal Article
European journal of medical genetics, ISSN 1769-7212, 11/2016, 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 | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | 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