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EVALUATION OF CLINICAL, DEMOGRAPHIC AND ELECTROENCEPHALOGRAPHY FINDINGS OF DRAVET SYNDROME PATIENTS

Objective: Dravet syndrome (DS) is a severe myoclonic epilepsy affecting infants and is classified among epileptic syndromes. Generally, the first seizures begin with febrile diseases during infancy. Cognitive functions and behavior of patients begin to decline from the age of two. In DS, the most c...

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Autors principals: Mahmut Aslan, Serdal Güngör
Format: Artigo
Idioma:Inglês
Publicat: Istanbul University Press 2021-01-01
Col·lecció:İstanbul Tıp Fakültesi Dergisi
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Accés en línia:https://cdn.istanbul.edu.tr/file/JTA6CLJ8T5/7552E42616C24921961E73FBE9972E73
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