X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1354) 1354
Book Review (409) 409
Publication (123) 123
Book Chapter (40) 40
Book / eBook (6) 6
Conference Proceeding (5) 5
Data Set (1) 1
Dissertation (1) 1
Journal / eJournal (1) 1
Magazine Article (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1099) 1099
humans (1013) 1013
progressive myoclonus epilepsy (677) 677
clinical neurology (605) 605
male (431) 431
female (423) 423
epilepsy (355) 355
neurosciences (343) 343
adult (305) 305
animals (304) 304
mutation (268) 268
adolescent (221) 221
middle aged (189) 189
biochemistry & molecular biology (188) 188
neurology (170) 170
myoclonus (167) 167
child (161) 161
disease (156) 156
genetics & heredity (152) 152
myoclonic epilepsies, progressive - genetics (148) 148
progressive external ophthalmoplegia (145) 145
gene (130) 130
mice (130) 130
electroencephalography (127) 127
lafora disease (121) 121
mutations (117) 117
phenotype (116) 116
seizures (114) 114
genetic aspects (113) 113
progressive myoclonic epilepsy (105) 105
diagnosis (103) 103
brain - pathology (100) 100
ataxia (99) 99
analysis (97) 97
cell biology (97) 97
lafora disease - genetics (97) 97
genetics (93) 93
pedigree (93) 93
dna, mitochondrial - genetics (90) 90
aged (85) 85
epm1 (85) 85
glycogen (82) 82
mutation - genetics (82) 82
young adult (79) 79
article (78) 78
magnetic resonance imaging (78) 78
mitochondrial dna (78) 78
research (77) 77
abridged index medicus (75) 75
child, preschool (75) 75
diagnosis, differential (74) 74
cystatin b (70) 70
proteins (70) 70
pathology (69) 69
genes (68) 68
neurodegeneration (68) 68
pediatrics (68) 68
anticonvulsants - therapeutic use (67) 67
nervous system diseases (65) 65
disease models, animal (64) 64
myoclonic epilepsies, progressive - physiopathology (63) 63
brain (61) 61
progressive supranuclear palsy (61) 61
unverricht-lundborg disease (61) 61
molecular sequence data (60) 60
dentatorubral-pallidoluysian atrophy (59) 59
ragged-red fibers (59) 59
myoclonic epilepsies, progressive - pathology (58) 58
cystatin-b (57) 57
dementia (57) 57
medicine & public health (57) 57
carrier proteins - genetics (56) 56
lafora disease - pathology (56) 56
physiological aspects (56) 56
age of onset (55) 55
lafora disease - metabolism (55) 55
myoclonic epilepsy (55) 55
mitochondrial diseases - genetics (54) 54
neurons (54) 54
epilepsies, myoclonic - genetics (52) 52
malin (52) 52
laforin (51) 51
mitochondria (51) 51
psychiatry (51) 51
infant (50) 50
unverricht-lundborg syndrome - genetics (50) 50
care and treatment (49) 49
genotype (49) 49
metabolism (49) 49
stroke-like episodes (49) 49
unverricht-lundborg-disease (48) 48
disease progression (47) 47
alzheimers-disease (46) 46
cystatin-b gene (46) 46
dna mutational analysis (46) 46
point mutation (46) 46
progressive myoclonus epilepsies (46) 46
amino acid sequence (45) 45
biopsy (45) 45
enzymes (45) 45
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1330) 1330
French (22) 22
Spanish (17) 17
Japanese (9) 9
German (4) 4
Czech (3) 3
Italian (3) 3
Russian (3) 3
Dutch (2) 2
Portuguese (2) 2
Turkish (2) 2
Chinese (1) 1
Croatian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 01/2015, Volume 47, Issue 1, pp. 39 - 46
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2008, Volume 83, Issue 5, pp. 572 - 581
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2008, Volume 82, Issue 3, pp. 673 - 684
Journal Article
Epilepsy Research, ISSN 0920-1211, 10/2019, Volume 156, pp. 106191 - 106191
Perampanel (PER) is a novel anti-seizure medication useful in different types of epilepsy. We intended to assess the effectiveness of PER on cortical myoclonus... 
EPM2 | Irritability | Progressive myoclonus epilepsy | Perampanel | Myoclonus scale | EPM1 | Index Medicus
Journal Article
Journal of Neurology, ISSN 0340-5354, 8/2014, Volume 261, Issue 8, pp. 1584 - 1597
Journal Article
Journal Article
Frontiers in Neurology, 09/2019, Volume 10
Juvenile myoclonic epilepsy (JME) is a common epilepsy syndrome characterized by bilateral myoclonic and tonic-clonic seizures typically starting in... 
epilepsy | genetics | pharmacoresistance |