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Spinal Muscular Atrophy With Myoclonic Epilepsy

Spinal muscular atrophy (SMA) is defined by degeneration of anterior horn cells in the spinal cord. Progressive myoclonic epilepsy (PME) is characterized by myoclonic and generalized seizures with progressive neurological deterioration. The association between SMA and PME has not yet been fully unde...

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Autori principali: Buket ÖZKARA, Faik BUDAK
Natura: Artigo
Lingua:Inglês
Pubblicazione: Turkish Epilepsy Society 2017-04-01
Serie:Archives of Epilepsy
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Accesso online: http://archepilepsy.org/archives/archive-detail/article-preview/spinal-muscular-atrophy-with-myoclonic-epilepsy/54995
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