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LANCET NEUROLOGY, ISSN 1474-4422, 01/2010, Volume 9, Issue 1, pp. 67 - 76
Background Some encephalitides or seizure disorders once thought idiopathic now seem to be immune mediated. We aimed to describe the clinical features of one... 
RESPONSES | BACLOFEN | TISSUE | GLOBUS-PALLIDUS | TRAFFICKING | MICE | CHANNELS | EPILEPSY | SYNAPTIC PLASTICITY | NMDAR ENCEPHALITIS | CLINICAL NEUROLOGY | Neurons - pathology | Rats, Wistar | Autoantibodies - blood | Humans | Middle Aged | Paraneoplastic Syndromes, Nervous System - immunology | Male | Seizures - metabolism | Autoimmune Diseases of the Nervous System - pathology | Lung Neoplasms | Brain - metabolism | Limbic Encephalitis - pathology | Paraneoplastic Syndromes, Nervous System - therapy | Limbic Encephalitis - therapy | Seizures - pathology | Receptors, GABA-B - immunology | Immunoglobulin G - immunology | Paraneoplastic Syndromes, Nervous System - pathology | Antigens, Surface - metabolism | Adult | Autoantibodies - analysis | Female | Immunoglobulin G - analysis | Neurons - metabolism | Autoimmune Diseases of the Nervous System - metabolism | Limbic Encephalitis - immunology | Cell Line | Receptors, GABA-B - genetics | Cells, Cultured | Neurons - immunology | Rats | Seizures - therapy | Autoimmune Diseases of the Nervous System - immunology | Autoantibodies - cerebrospinal fluid | Limbic Encephalitis - metabolism | Animals | Seizures - immunology | Brain - pathology | Aged | Autoimmune Diseases of the Nervous System - therapy | Antigens, Surface - immunology | Brain - immunology | Receptors, GABA-B - metabolism | Index Medicus | MEDICIN OCH HÄLSOVETENSKAP | MEDICAL AND HEALTH SCIENCES
Journal Article
British Journal of Dermatology, ISSN 0007-0963, 12/2015, Volume 173, Issue 6, pp. 1505 - 1513
Journal Article
Journal Article
Journal Article
Pediatric Neurology, ISSN 0887-8994, 01/2018, Volume 78, pp. 35 - 40
Aicardi-Goutières syndrome is a rare genetic neurological disorder with variable clinical manifestations. Molecular detection of specific mutations is required... 
leukodystrophy | calcification | TREX-1 | Aicardi-Goutières syndrome | TREX1 | DISORDERS | PROGRESSIVE FAMILIAL ENCEPHALOPATHY | SAMHD1 | CLINICAL NEUROLOGY | IFIH1 | INTERFERON-ALPHA | METABOLISM | Aicardi-Goutieres syndrome | DISEASE | PEDIATRICS | INFECTION | MUTATIONS | Ribonucleases - genetics | Seizures - genetics | Humans | Atrophy - pathology | Child, Preschool | Infant | Male | Neurodevelopmental Disorders - genetics | Epilepsy - physiopathology | Autoimmune Diseases of the Nervous System - pathology | Epilepsy - etiology | Libya | Saudi Arabia | Autoimmune Diseases of the Nervous System - physiopathology | Seizures - physiopathology | Seizures - pathology | Qatar | Autoimmune Diseases of the Nervous System - genetics | Nervous System Malformations - physiopathology | Epilepsy - genetics | Female | Nervous System Malformations - genetics | Child | Neurodevelopmental Disorders - etiology | Nervous System Malformations - pathology | Neurodevelopmental Disorders - physiopathology | United Arab Emirates | Muscle Spasticity - pathology | Autoimmune Diseases of the Nervous System - complications | White Matter - pathology | Muscle Spasticity - etiology | Nervous System Malformations - complications | Seizures - etiology | Consanguinity | Muscle Spasticity - physiopathology | Epilepsy - pathology | Muscle Spasticity - genetics | Medicine, Experimental | Medical research | Nervous system diseases | Arab countries | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 02/2003, Volume 421, Issue 6924, pp. 744 - 748
Journal Article
Journal of immunology (Baltimore, Md, ISSN 0022-1767, 2015, Volume 194, Issue 8, pp. 3623 - 3633
Aicardi-Goutières syndrome (AGS) is a monogenic inflammatory encephalopathy caused by mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, or MDA5.... 
INTERFERON-ALPHA | ACTIVATION | TREX1 | DNA | MUTATIONS | IMMUNOLOGY | SAMHD1 | RIBONUCLEOTIDES | ASTROCYTES | EXPRESSION | CEREBRAL VASCULOPATHY | Phosphoproteins - immunology | RNA-Binding Proteins - genetics | Exodeoxyribonucleases - immunology | Nervous System Malformations - immunology | Humans | Astrocytes - pathology | SAM Domain and HD Domain-Containing Protein 1 | Monomeric GTP-Binding Proteins - immunology | Autoimmune Diseases of the Nervous System - pathology | Autoimmune Diseases of the Nervous System - mortality | Ribonuclease H - immunology | Neural Stem Cells - immunology | Astrocytes - immunology | Interferon-alpha - genetics | Autoimmune Diseases of the Nervous System - genetics | HEK293 Cells | Exodeoxyribonucleases - genetics | Nervous System Malformations - genetics | Cytokines - genetics | Cytokines - immunology | Ribonuclease H - genetics | Adenosine Deaminase - genetics | Nervous System Malformations - pathology | RNA-Binding Proteins - immunology | Gene Silencing | Monomeric GTP-Binding Proteins - genetics | Phosphoproteins - genetics | Neural Stem Cells - pathology | Interferon-alpha - immunology | Endothelial Cells - immunology | Autoimmune Diseases of the Nervous System - immunology | Nervous System Malformations - mortality | Mutation | Endothelial Cells - pathology | Adenosine Deaminase - immunology | Index Medicus | Abridged Index Medicus
Journal Article
NEUROLOGY, ISSN 0028-3878, 10/2005, Volume 65, Issue 8, pp. 1184 - 1188
Background: Narcolepsy with cataplexy is associated with a loss of orexin/hypocretin. It is speculated that an autoimmune process kills the orexin-producing... 
SYSTEM | OBESITY | MUTATION | GENE-EXPRESSION | HYPOCRETIN NEURONS | KNOCKOUT MICE | CODEINE | CLINICAL NEUROLOGY | HYPOTHALAMUS | Immunohistochemistry | Neurons - pathology | Dynorphins - genetics | Humans | Middle Aged | Nerve Tissue Proteins - deficiency | Nerve Degeneration - physiopathology | Nerve Degeneration - genetics | Intracellular Signaling Peptides and Proteins - immunology | Male | Neural Pathways - pathology | RNA, Messenger - metabolism | Autoimmune Diseases of the Nervous System - pathology | Narcolepsy - etiology | Narcolepsy - physiopathology | Intracellular Signaling Peptides and Proteins - deficiency | Autoimmune Diseases of the Nervous System - physiopathology | C-Reactive Protein - deficiency | Neurons - metabolism | Neural Pathways - physiopathology | Neuropeptides - genetics | Intracellular Signaling Peptides and Proteins - genetics | Narcolepsy - pathology | Neuropeptides - deficiency | Neurodegenerative Diseases - pathology | Nerve Tissue Proteins - immunology | Orexins | Dynorphins - deficiency | C-Reactive Protein - genetics | Hypothalamus - pathology | Hypothalamus - physiopathology | Nerve Tissue Proteins - genetics | Neurodegenerative Diseases - complications | Nerve Degeneration - pathology | Autoimmune Diseases of the Nervous System - complications | Dynorphins - immunology | Autoantibodies - immunology | Hypothalamus - metabolism | Neurodegenerative Diseases - physiopathology | Brain Mapping | Neural Pathways - metabolism | Aged | Neuropeptides - immunology | C-Reactive Protein - immunology | Index Medicus | Abridged Index Medicus
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 2017, Volume 45, Issue 8, pp. 4619 - 4631
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 06/2016, Volume 213, Issue 7, pp. 1163 - 1174
Journal Article