Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental models - Test2 - elhamkhani - TriplyDB

Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental models

Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental models

http://www.wikidata.org/entity/Q26861471

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The genetic relationship between epilepsy and hemiplegic migraine Genetic basis of pediatric epilepsy syndromes.Action potential initiation in neocortical inhibitory interneurons.Animal Models of Seizures and Epilepsy: Past, Present, and Future Role for the Discovery of Antiseizure Drugs.Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations.Models for discovery of targeted therapy in genetic epileptic encephalopathies.Novel concepts in epileptogenesis and its prevention.

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Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental models

http://www.wikidata.org/entity/Q26861471

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2014 nî lūn-bûn

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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2014 թվականի ապրիլին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Genetic epilepsy syndromes wit ...... atures and experimental models

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Genetic epilepsy syndromes wit ...... atures and experimental models

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Genetic epilepsy syndromes wit ...... atures and experimental models

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Genetic epilepsy syndromes wit ...... atures and experimental models

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S13311-014-0267-0

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Neurotherapeutics

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Genetic epilepsy syndromes wit ...... atures and experimental models

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Carla Marini

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Renzo Guerrini

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P2860

A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy

A Tumor suppressor complex with GAP activity for the Rag GTPases that signal amino acid sufficiency to mTORC1

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

A potassium channel mutation in neonatal human epilepsy

Radicals r'aging.

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269-285

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2

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Massimo Mantegazza

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