Neuropsychological findings in patients with Unverricht–Lundborg disease-Reference-Cited by-同舟云学术

Neuropsychological findings in patients with Unverricht–Lundborg disease

Published:2009-03 Issue:3 Volume:14 Page:545-549
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Ferlazzo Edoardo,Gagliano Antonella,Calarese Tiziana,Magaudda Adriana,Striano Pasquale,Cortese Lara,Cedro Clemente,Laguitton Virgilie,Bramanti Placido,Carbonaro Marilena,Albachiara Addolorata,Fragassi Nina,Italiano Domenico,Sessa Edoardo,Coppola Antonietta,Genton Pierre

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Neurology (clinical),Neurology

Reference35 articles.

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3. Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1);Pennacchio;Science,1996

4. A new clinical and molecular form of Unverricht–Lundborg disease localized by homozygosity mapping;Berkovic;Brain,2005

5. A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy–ataxia syndrome;Bassuk;Am J Hum Genet,2008

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