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Epilepsy & behavior : E&B, ISSN 1525-5050, 4/2018, Volume 81, pp. 125 - 127
Journal Article
06/2012
Lafora disease (LD) is an adolescent-onset autosomal recessive progressive myoclonus epilepsy. The main clinical symptoms of the disease are worsening... 
0369 | 0379 | Glycogen | Epilepsy | 0307 | Lafora disease | 0317
Dissertation
Brain stimulation, ISSN 1935-861X, 08/2019
Journal Article
Trends in Molecular Medicine, ISSN 1471-4914, 09/2019
Journal Article
The Application of Clinical Genetics, ISSN 1178-704X, 05/2016, Volume 2016, Issue Issue 1, pp. 49 - 53
Miljana Kecmanović,1 Milica Keckarević-Marković,1 Dušan Keckarević,1 Galina Stevanović,2 Nebojša Jović,2 Stanka Romac,1,† 1Faculty of Biology, Center for Human... 
treatment | glycogen synthase | Lafora disease
Journal Article
Dusunen Adam, ISSN 1018-8681, 2016, Volume 29, Issue 2, pp. 173 - 176
Journal Article
Neuroreport, ISSN 0959-4965, 3/2017, Volume 28, Issue 5, pp. 268 - 271
Lafora disease (LD) is a rare adolescent-onset progressive myoclonic epilepsy caused by loss-of-function mutations either in the EPM2A gene encoding laforin or... 
epilepsy | malin knockout mouse | autophagy | oxidative stress | PTZ | Lafora disease
Journal Article
Cell Metabolism, ISSN 1550-4131, 10/2019, Volume 30, Issue 4, pp. 689 - 705.e6
Lafora disease (LD) is a fatal childhood epilepsy caused by recessive mutations in either the or gene. A hallmark of LD is the intracellular accumulation of... 
epilepsy | enzyme therapy | antibody-enzyme fusion | metabolomics | Lafora bodies | glycogen storage disease | glycogen | amylase | antibody-based drug | Lafora disease
Journal Article
Iranian journal of child neurology, ISSN 1735-4668, 2019, Volume 13, Issue 1, pp. 115 - 120
Lafora progressive myoclonus epilepsy (Lafora disease, LD) is a fatal autosomal recessive neurodegenerative disorder (with an onset in teenage years in... 
Progressive myoclonus epilepsy | NHLRC1 mutation | Case Report | Lafora disease
Journal Article
Nature Immunology, ISSN 1529-2908, 12/2012, Volume 13, Issue 12, pp. 1178 - 1186
Journal Article
PLOS ONE, ISSN 1932-6203, 01/2018, Volume 13, Issue 1
Ostreococcus tauri, the smallest free-living (non-symbiotic) eukaryote yet described, is a unicellular green alga of the Prasinophyceae family. It has a very... 
GLUCAN PHOSPHATASES | SEX FOUR2 | ARABIDOPSIS-THALIANA | LAFORA DISEASE | METABOLISM | MULTIDISCIPLINARY SCIENCES | R1 PROTEIN | GREEN-ALGAE | STARCH DEPHOSPHORYLATION | PROTEIN-TYROSINE-PHOSPHATASE | 3-DIMENSIONAL STRUCTURES
Journal Article
Experimental Neurology, ISSN 0014-4886, 10/2019, Volume 320, p. 112959
Lafora disease (LD) is a fatal rare neurodegenerative disorder characterized by epilepsy, neurodegeneration and insoluble polyglucosan accumulation in brain... 
Epileptogenesis | c-fos | Glutamate transport | Lafora disease | GLT-1 | PROGRESSIVE MYOCLONUS EPILEPSY | NMDA RECEPTOR BLOCKADE | PROTEIN | MALIN-DEFICIENT MICE | RAT | NEUROSCIENCES | PREFRONTAL CORTEX | AMINO-ACID TRANSPORTER | EXPRESSION | BRAIN
Journal Article
Current Pharmaceutical Design, ISSN 1381-6128, 01/2017, Volume 23, Issue 37, pp. 5662 - 5666
Journal Article
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