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1. Full Text Candidate genes for temporal lobe epilepsy: a replication study
by Salzmann, Annick and Perroud, Nader and Crespel, Arielle and Lambercy, Carmen and Malafosse, Alain
Neurological sciences, ISSN 1590-1874, 12/2008, Volume 29, Issue 6, pp. 397 - 403
Neurology | Prodynorphin | Association | Medicine & Public Health | Apolipoprotein E | Interleukin 1 | Temporal lobe epilepsy | Genetics | Neurosurgery | Psychiatry | Neuroradiology | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease - genetics | Genetic Testing | Protein Precursors - genetics | Gene Frequency | Humans | Epilepsy, Temporal Lobe - physiopathology | Genotype | Interleukin 1 Receptor Antagonist Protein - genetics | Epilepsy, Temporal Lobe - immunology | Interleukin-1beta - genetics | Case-Control Studies | Enkephalins - genetics | Interleukins - genetics | DNA Mutational Analysis | Apolipoproteins E - genetics | Epilepsy, Temporal Lobe - genetics | Genetic Markers - genetics | Adolescent | Adult | Polymorphism, Genetic - genetics | Interleukin-1alpha - genetics | Child | Cohort Studies | Genetic research | Interleukins | Apolipoproteins | Medical genetics | Index Medicus
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2. Full Text Pharmaco-genetic therapeutics targeting parvalbumin neurons attenuate temporal lobe epilepsy
by Wang, Ying and Liang, Jiao and Chen, Liying and Shen, Yating and Zhao, Junli and Xu, Cenglin and Wu, Xiaohua and Cheng, Heming and Ying, Xiaoying and Guo, Yi and Wang, Shuang and Zhou, Yudong and Wang, Yi and Chen, Zhong
Neurobiology of disease, ISSN 0969-9961, 09/2018, Volume 117, pp. 149 - 160
Temporal lobe epilepsy | Parvalbumin neurons | Pharmaco-genetic | Pyramidal neurons | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Pharmacogenetics - methods | Neurons - chemistry | Epilepsy, Temporal Lobe - drug therapy | Parvalbumins - metabolism | Anticonvulsants - administration & dosage | Male | Mice, Transgenic | Epilepsy, Temporal Lobe - metabolism | GABA-A Receptor Antagonists - administration & dosage | Dose-Response Relationship, Drug | Animals | Parvalbumins - analysis | Epilepsy, Temporal Lobe - genetics | Parvalbumins - genetics | Mice | Neurons - metabolism | Neurons - drug effects | Medical colleges | Neurons | Analysis | Therapeutics | Genetic research | Seizures (Medicine) | Neurophysiology | Homeopathy | Materia medica and therapeutics | Index Medicus
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3. Full Text Dynorphin‐based “release on demand” gene therapy for drug‐resistant temporal lobe epilepsy
by Agostinho, Alexandra S and Mietzsch, Mario and Zangrandi, Luca and Kmiec, Iwona and Mutti, Anna and Kraus, Larissa and Fidzinski, Pawel and Schneider, Ulf C and Holtkamp, Martin and Heilbronn, Regine and Schwarzer, Christoph
EMBO molecular medicine, ISSN 1757-4676, 10/2019, Volume 11, Issue 10, pp. e9963 - n/a
adeno‐associated virus | learning | memory | seizure | neuropeptide | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Models, Theoretical | Dependovirus - genetics | Gene Expression | Transduction, Genetic | Dynorphins - genetics | Humans | Gene Expression Regulation | Rats | Treatment Outcome | Neurotransmitter Agents - genetics | Animals | Neurotransmitter Agents - pharmacology | Epilepsy, Temporal Lobe - therapy | Dynorphins - pharmacology | Mice | Genetic Vectors | Organ Culture Techniques | Disease Models, Animal | Genetic Therapy - methods | Genetic vectors | Comorbidity | Analysis | Genes | Neuropeptides | Temporal lobe epilepsy | Seizures (Medicine) | Drug resistance | Drug therapy | Gene therapy | Drugs | Patents | Temporal lobe | Medical research | Animal models | Peptides | Narcotics | Epilepsy | Memory | Spatial discrimination learning | Gene expression | Vectors (Biology) | Habituation | Convulsions & seizures | Surgery | Dynorphin | preprodynorphin | Hippocampus | Seizures | Spatial memory | Animal cognition | Index Medicus | Neuroscience | Genetics, Gene Therapy & Genetic Disease
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4. Full Text Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations
by Scheffer, Ingrid E and Harkin, Louise A and Grinton, Bronwyn E and Dibbens, Leanne M and Turner, Samantha J and Zielinski, Marta A and Xu, Ruwei and Jackson, Graeme and Adams, Judith and Connellan, Mary and Petrou, Steven and Wellard, R. Mark and Briellmann, Regula S and Wallace, Robyn H and Mulley, John C and Berkovic, Samuel F
Brain (London, England : 1878), ISSN 0006-8950, 01/2007, Volume 130, Issue 1, pp. 100 - 109
Genetics | GEFS | Sodium channel | TLE | Epilepsy | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Neurology | Biological and medical sciences | Medical sciences | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Nervous system (semeiology, syndromes) | Epilepsy, Generalized - genetics | Seizures - genetics | Humans | Child, Preschool | Magnetic Resonance Imaging - methods | Family Health | Genotype | Infant | Male | Voltage-Gated Sodium Channel beta-1 Subunit | Mutation, Missense - genetics | Point Mutation - genetics | Phenotype | Pedigree | Epilepsy, Temporal Lobe - genetics | Adolescent | Age of Onset | Adult | Female | Sodium Channels - genetics | Child | Index Medicus | Abridged Index Medicus
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5. Full Text Familial mesial temporal lobe epilepsy (FMTLE)
: A clinical and genetic study of 15 Italian families
by Striano, P and Striano, P and Gambardella, A and Gambardella, A and Coppola, A and Coppola, A and Di Bonaventura, C and Di Bonaventura, C and Bovo, G and Bovo, G and Diani, E and Diani, E and Boaretto, F and Boaretto, F and Egeo, G and Egeo, G and Ciampa, C and Ciampa, C and Labate, A and Labate, A and Testoni, S and Testoni, S and Passarelli, D and Passarelli, D and Manna, I and Manna, I and Sferro, C and Sferro, C and Aguglia, U and Aguglia, U and Caranci, F and Caranci, F and Giallonardo, A T and Giallonardo, A T and Striano, S and Striano, S and Nobile, C and Nobile, C and Michelucci, R and Michelucci, R
Journal of neurology, ISSN 0340-5354, 1/2008, Volume 255, Issue 1, pp. 16 - 23
epilepsy | Neurology | Neurosciences | temporal lobe epilepsy | genetics | Medicine & Public Health | hippocampal sclerosis | FMTLE | linkage | Neuroradiology | Hippocampal sclerosis | Genetics | Temporal lobe epilepsy | Linkage | Epilepsy | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Biological and medical sciences | Medical sciences | Nervous system (semeiology, syndromes) | Sensation Disorders - physiopathology | Genetic Testing | Humans | Middle Aged | Epilepsy, Temporal Lobe - physiopathology | Male | Electroencephalography | DNA Mutational Analysis | Neurocognitive Disorders - genetics | Epilepsy, Temporal Lobe - genetics | Aged, 80 and over | Inheritance Patterns - genetics | Adult | Female | Temporal Lobe - pathology | Child | Chromosome Disorders - physiopathology | Epilepsy, Temporal Lobe - pathology | Chromosome Disorders - pathology | Genetic Predisposition to Disease - genetics | Neurocognitive Disorders - physiopathology | Genotype | Chromosome Mapping | Mutation - genetics | Temporal Lobe - physiopathology | Pedigree | Adolescent | Italy | Aged | Sensation Disorders - genetics | Genes, Dominant - genetics | Chromosome Disorders - genetics | Usage | Care and treatment | Magnetic resonance imaging | Diagnosis | Research | Health aspects | Index Medicus
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6. Full Text Neuron‐restrictive silencer factor‐mediated hyperpolarization‐activated cyclic nucleotide gated channelopathy in experimental temporal lobe epilepsy
by McClelland, Shawn and Flynn, Corey and Dubé, Celine and Richichi, Cristina and Zha, Qinqin and Ghestem, Antoine and Esclapez, Monique and Bernard, Christophe and Baram, Tallie Z
Annals of neurology, ISSN 0364-5134, 09/2011, Volume 70, Issue 3, pp. 454 - 465
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Neurology | Biological and medical sciences | Medical sciences | Nervous system (semeiology, syndromes) | Nucleotides, Cyclic - metabolism | Dendrites - pathology | Excitatory Amino Acid Agonists | Rats, Wistar | Channelopathies - physiopathology | Gene Expression - genetics | Potassium Channels - physiology | Status Epilepticus - chemically induced | Epilepsy, Temporal Lobe - physiopathology | Male | Channelopathies - metabolism | Repressor Proteins - antagonists & inhibitors | Kainic Acid | Repressor Proteins - physiology | CA1 Region, Hippocampal - pathology | Ion Channel Gating - physiology | Gene Expression - physiology | Epilepsy, Temporal Lobe - chemically induced | Cyclic Nucleotide-Gated Cation Channels - genetics | Cyclic Nucleotide-Gated Cation Channels - physiology | Rats | Epilepsy, Temporal Lobe - metabolism | Hippocampus - pathology | Chromatin - pathology | Potassium Channels - genetics | Channelopathies - genetics | Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels | Animals | Status Epilepticus - physiopathology | Status Epilepticus - metabolism | Chromatin | Epilepsy | Index Medicus
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7. Full Text Astrocyte dysfunction in temporal lobe epilepsy: K+ channels and gap junction coupling
by Steinhäuser, Christian and Seifert, Gerald and Bedner, Peter
Glia, ISSN 0894-1491, 08/2012, Volume 60, Issue 8, pp. 1192 - 1202
astroglia | Cx30 | Kir4.1 | Cx43 | hemichannel | Kir channel | dye coupling | connexin | Connexin | Astroglia | Dye coupling | Hemichannel | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Potassium Channels - metabolism | Animals | Gap Junctions - physiology | Epilepsy, Temporal Lobe - genetics | Humans | Astrocytes - pathology | Connexins - genetics | Mutation - genetics | Epilepsy, Temporal Lobe - pathology | Astrocytes - metabolism | Connexins - metabolism | Potassium Channels - genetics | Index Medicus
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