Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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name

Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

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Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

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Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

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Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

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Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

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Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

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P1476

Epilepsy with auditory features: A heterogeneous clinico-molecular disease

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Chiara Leta

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Francesca Bisulli

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Giovanni Boero

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Giuseppe d'Orsi

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Ingrid Scheffer

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Laura Licchetta

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Marco Seri

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Paolo Tinuper

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Sara Baldassari

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Tommaso Pippucci

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De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan's syndrome and acquired neuromyotonia

The involvement of Reelin in neurodevelopmental disorders.

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

Localization of a gene for partial epilepsy to chromosome 10q

Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation

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10.1212/NXG.0000000000000005

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2015-05-14T00:00:00Z

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27066544

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4821078

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