Pages that link to "Q28211213"
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The following pages link to Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+? (Q28211213):
Displaying 50 items.
- Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancy (Q24563329) (← links)
- Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus (Q24632952) (← links)
- (Q28178529) (redirect page) (← links)
- Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A (Q28191292) (← links)
- Generalized epilepsy with febrile seizures plus type 2 mutation W1204R alters voltage-dependent gating of Na(v)1.1 sodium channels (Q28204139) (← links)
- Long-term efficacy and tolerance of stiripentaol in severe myoclonic epilepsy of infancy (Dravet's syndrome) (Q28219202) (← links)
- Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB) (Q28240097) (← links)
- SCN1A mutations and epilepsy (Q28249270) (← links)
- An epilepsy mutation in the sodium channel SCN1A that decreases channel excitability (Q28300929) (← links)
- Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy (Q28585126) (← links)
- Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus (Q30498134) (← links)
- Seizure Reduction with Fluoxetine in Dravet Syndrome. (Q33773087) (← links)
- Inherited disorders of voltage-gated sodium channels (Q33905815) (← links)
- Infantile seizures and epilepsy syndromes (Q34132903) (← links)
- Epileptic syndromes in childhood: clinical features, outcomes, and treatment (Q34132909) (← links)
- Genetics of epilepsy: The testimony of twins in the molecular era (Q34198753) (← links)
- Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome (Q34359072) (← links)
- Identification of epilepsy genes in human and mouse (Q34432267) (← links)
- Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome). (Q34432842) (← links)
- Epilepsy in children (Q34493734) (← links)
- Diagnostic difficulty in infants and children (Q34579431) (← links)
- The genetic and molecular basis of epilepsy (Q35192541) (← links)
- The genetics of human epilepsy (Q35198044) (← links)
- Classification of seizures and epilepsy (Q35204002) (← links)
- Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome (Q35375026) (← links)
- Monogenic idiopathic epilepsies (Q35708106) (← links)
- Molecular basis of Mendelian idiopathic epilepsies (Q35761311) (← links)
- Genes and mutations in human idiopathic epilepsy (Q35766434) (← links)
- Etiologic factors and clinical features of symptomatic epilepsy: focus on pediatric cases (Q35776366) (← links)
- Fever, genes, and epilepsy (Q35811060) (← links)
- Inherited Channelopathies Associated with Epilepsy (Q35962079) (← links)
- Genetics of idiopathic generalized epilepsies (Q36319378) (← links)
- Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+). (Q36344246) (← links)
- Neonatal epilepsy syndromes and GEFS+: mechanistic considerations (Q36344256) (← links)
- Phenotype definition in epilepsy (Q36404635) (← links)
- Multiplex families with epilepsy: Success of clinical and molecular genetic characterization (Q36607672) (← links)
- Navigating the channels and beyond: unravelling the genetics of the epilepsies (Q37085097) (← links)
- CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation (Q37347828) (← links)
- Medical management of Lennox-Gastaut syndrome (Q37693139) (← links)
- GABRA1 and STXBP1: novel genetic causes of Dravet syndrome (Q37725930) (← links)
- Hereditary Channelopathies in Neurology (Q37786254) (← links)
- The genetics of Dravet syndrome. (Q37861258) (← links)
- Dravet syndrome: insights from in vitro experimental models. (Q37861268) (← links)
- Molecular genetics of Dravet syndrome (Q37866829) (← links)
- Genetics of epilepsy and relevance to current practice (Q38012351) (← links)
- A hot topic: temperature sensitive sodium channelopathies (Q38014193) (← links)
- Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy (Q38566303) (← links)
- The genetic landscape of the epileptic encephalopathies of infancy and childhood. (Q38644331) (← links)
- Genetic Testing in Pediatric Epilepsy (Q38838914) (← links)
- Dravet Syndrome: Diagnosis and Long-Term Course. (Q38855478) (← links)