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Article

[Importance of molecular genetics in refractory epilepsy in infants with a normal phenotype].

Revista de neurologia - 1 Aug 2014

de Santiago García-Caro Eloísa, Martínez-Antón Jacinto

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PMID: 25030075

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Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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[Importance of molecular genetics in refractory epilepsy in infants with a normal phenotype].PMID 25030075Read ↗

[Development of the molecular genetics of epilepsy].Semantic proximity Read ↗

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[The clinical utility of genetic testing in epilepsy].Semantic proximity Read ↗

[Molecular genetics of intractable epilepsies].Semantic proximity Read ↗

[Genetic etiologies associated with severe epilepsies in infancy].Semantic proximity Read ↗

[Progress in molecular genetics of epilepsy].Semantic proximity Read ↗

[Contributions and expectations of molecular genetics in perinatal neurologic diagnosis].Semantic proximity Read ↗

[Molecular genetic understanding of hereditary disorders].Semantic proximity Read ↗

[Genetic variations and epilepsy].Semantic proximity Read ↗

[Interstitial lung disease in infants caused by genetic abnormalities].Semantic proximity Read ↗

[Molecular genetic causes of epilepsy in children].Semantic proximity Read ↗

Genetic diagnosis in neonatal-onset epilepsies: Back to the future.Semantic proximity Read ↗

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