X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (580) 580
Publication (104) 104
Book Chapter (7) 7
Book Review (4) 4
Dissertation (2) 2
Book / eBook (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (335) 335
lafora disease (262) 262
index medicus (228) 228
progressive myoclonus epilepsy (202) 202
epilepsy (163) 163
animals (162) 162
clinical neurology (161) 161
male (157) 157
lafora disease - genetics (152) 152
female (144) 144
glycogen (126) 126
adolescent (117) 117
mutation (102) 102
adult (101) 101
mice (92) 92
lafora disease - pathology (91) 91
neurosciences (87) 87
biochemistry & molecular biology (84) 84
lafora disease - metabolism (80) 80
disease (70) 70
mutations (70) 70
carrier proteins - genetics (68) 68
malin (67) 67
laforin (66) 66
lafora disease - diagnosis (62) 62
metabolism (62) 62
child (61) 61
glycogen - metabolism (60) 60
bodies (59) 59
gene (59) 59
phosphatase (58) 58
myoclonus (55) 55
biopsy (51) 51
article (50) 50
electroencephalography (50) 50
lafora disease - physiopathology (50) 50
protein tyrosine phosphatases, non-receptor - genetics (50) 50
genetics & heredity (49) 49
skin biopsy (47) 47
phosphorylation (46) 46
seizures (45) 45
cell biology (44) 44
neurodegeneration (44) 44
neurology (44) 44
lafora-disease (43) 43
proteins (43) 43
analysis (42) 42
diagnosis (42) 42
pathology (42) 42
autophagy (40) 40
protein tyrosine phosphatases - genetics (40) 40
degradation (39) 39
disease models, animal (39) 39
epm2a (39) 39
mice, knockout (39) 39
middle aged (39) 39
protein tyrosine phosphatases, non-receptor (39) 39
corpora-amylacea (37) 37
lafora bodies (37) 37
polyglucosan bodies (37) 37
progressive myoclonic epilepsy (37) 37
protein tyrosine phosphatases, non-receptor - metabolism (37) 37
brain (36) 36
carrier proteins - metabolism (36) 36
e3 ubiquitin ligase (35) 35
brain - pathology (34) 34
genetic aspects (34) 34
phosphatases (34) 34
glucans - metabolism (33) 33
skin - pathology (32) 32
dual-specificity phosphatase (31) 31
dual-specificity phosphatases - metabolism (31) 31
physiological aspects (31) 31
congenital, hereditary, and neonatal diseases and abnormalities (30) 30
epm2a gene (30) 30
inclusion bodies - metabolism (30) 30
nervous system diseases (30) 30
glycogen-synthesis (29) 29
lafora's disease (29) 29
ubiquitin (29) 29
enzymes (28) 28
epilepsies, myoclonic - pathology (28) 28
glucose (28) 28
molecular sequence data (28) 28
diagnosis, differential (27) 27
glycogen synthase - metabolism (27) 27
lafora (27) 27
lafora disease - complications (27) 27
myoclonic epilepsy (27) 27
accumulation (26) 26
inclusion bodies - ultrastructure (26) 26
research (26) 26
dual-specificity phosphatases - genetics (25) 25
genes (25) 25
glycogen synthase (25) 25
inclusion bodies - pathology (25) 25
protein (25) 25
disease progression (24) 24
lafora disease - enzymology (24) 24
microscopy, electron (24) 24
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (504) 504
Spanish (34) 34
French (20) 20
Portuguese (10) 10
Japanese (4) 4
Turkish (4) 4
German (3) 3
Italian (3) 3
Russian (2) 2
Croatian (1) 1
Korean (1) 1
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Pediatric Research, ISSN 0031-3998, 2014, Volume 75, Issue 1-2, pp. 217 - 226
Journal Article
Brain, ISSN 0006-8950, 2012, Volume 135, Issue 9, pp. 2684 - 2698
Journal Article
Molecular Aspects of Medicine, ISSN 0098-2997, 12/2015, Volume 46, pp. 78 - 84
Journal Article
Journal Article
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