EPILEPSIA,volume 56,issue 5  (05-2015)

Period of time： 2015年5期

Publisher： John Wiley & Sons Inc

Founded in： 1909

Total resources： 57

E-ISSN： 1528-1167|56|5

ISSN： 0013-9580

Subject： R Medicine and Health

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EPILEPSIA,volume 56,issue 5

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Effects of chronic administration of valproic acid to epileptic patients on coagulation tests and primary hemostasis

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. e49-e52

John Wiley & Sons Inc

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The performance of three mortality risk‐adjustment comorbidity indices in a community epilepsy cohort

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. e68-e72

John Wiley & Sons Inc

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Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. e53-e57

John Wiley & Sons Inc

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Does adherence to epilepsy quality measures correlate with reduced epilepsy‐related adverse hospitalizations? A retrospective experience

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. e63-e67

John Wiley & Sons Inc

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Distribution of seizures across the menstrual cycle in women with epilepsy

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. e58-e62

John Wiley & Sons Inc

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Research priorities in epilepsy for the Asia‐Oceanian region

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. 667-673

John Wiley & Sons Inc

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Indications and expectations for neuropsychological assessment in routine epilepsy care: Report of the ILAE Neuropsychology Task Force, Diagnostic Methods Commission, 2013–2017

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. 674-681

John Wiley & Sons Inc

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The Jack Pribaz Foundation and KCNQ2.org

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. 682-684

John Wiley & Sons Inc

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Early and effective treatment of KCNQ2 encephalopathy

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. 685-691

John Wiley & Sons Inc

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Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1

EPILEPSIA,volume 56,issue 5 , Vol. 56, Iss. 5, 2015-05 , pp. 692-698

John Wiley & Sons Inc

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