X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (687) 687
Book Review (69) 69
Publication (53) 53
Book Chapter (5) 5
Patent (4) 4
Book / eBook (2) 2
Conference Proceeding (1) 1
Report (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (439) 439
humans (419) 419
clinical neurology (306) 306
male (284) 284
female (274) 274
epilepsy (259) 259
adult (206) 206
neurosciences (141) 141
adolescent (140) 140
seizures (140) 140
child (119) 119
mutation (111) 111
middle aged (109) 109
abridged index medicus (102) 102
pedigree (102) 102
child, preschool (94) 94
genetics (93) 93
epilepsy - genetics (92) 92
genetic aspects (80) 80
electroencephalography (75) 75
neurology (68) 68
phenotype (68) 68
infant (62) 62
magnetic resonance imaging (60) 60
young adult (59) 59
genetics & heredity (58) 58
mutation - genetics (56) 56
animals (53) 53
mutations (51) 51
brain (45) 45
aged (41) 41
article (40) 40
epilepsy, generalized - genetics (40) 40
gene (40) 40
genes (39) 39
analysis (38) 38
age of onset (37) 37
temporal-lobe epilepsy (37) 37
cohort studies (36) 36
generalized epilepsy (36) 36
genetic research (36) 36
research (36) 36
syndrome (35) 35
children (34) 34
epilepsies, myoclonic - genetics (32) 32
seizures, febrile - genetics (32) 32
anticonvulsants - therapeutic use (31) 31
epilepsy - diagnosis (31) 31
febrile seizures (31) 31
idiopathic generalized epilepsy (31) 31
diagnosis (30) 30
genetic predisposition to disease (30) 30
risk factors (30) 30
mice (29) 29
severe myoclonic epilepsy (29) 29
de-novo mutations (28) 28
epilepsies, partial - genetics (28) 28
epilepsy - physiopathology (28) 28
family (28) 28
frontal-lobe epilepsy (28) 28
gene mutations (28) 28
genotype (28) 28
nerve tissue proteins - genetics (28) 28
sodium channels - genetics (28) 28
childhood absence epilepsy (27) 27
eeg (27) 27
genetic predisposition to disease - genetics (26) 26
juvenile myoclonic epilepsy (26) 26
treatment outcome (26) 26
genetic linkage (25) 25
dna mutational analysis (24) 24
febrile seizures plus (24) 24
diagnosis, differential (23) 23
medical research (23) 23
seizures - genetics (23) 23
classification (22) 22
convulsions (22) 22
encephalopathy (22) 22
hippocampus - pathology (22) 22
epilepsy, temporal lobe - diagnosis (21) 21
retrospective studies (21) 21
sclerosis (21) 21
convulsions & seizures (20) 20
disease (20) 20
epilepsy - drug therapy (20) 20
expression (20) 20
family health (20) 20
medicine, general & internal (20) 20
molecular sequence data (20) 20
receptors, gaba-a - genetics (20) 20
scn1a (20) 20
chromosome mapping (19) 19
time factors (19) 19
age (18) 18
biochemistry & molecular biology (18) 18
brain - pathology (18) 18
infant, newborn (18) 18
intellectual disability (18) 18
epilepsy - etiology (17) 17
epilepsy, temporal lobe - physiopathology (17) 17
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1999, Current problems in epilepsy, ISBN 0861965698, Volume 13., viii, 286
Book
The New England Journal of Medicine, ISSN 0028-4793, 05/2017, Volume 376, Issue 21, pp. 2075 - 2076
Journal Article
Epileptic disorders : international epilepsy journal with videotape, ISSN 1294-9361, 12/2018, Volume 20, Issue 6, pp. 456 - 456
Journal Article
Epilepsy Research, ISSN 0920-1211, 09/2019, Volume 155, pp. 106154 - 106154
To describe the characteristics of a patient group who, after temporal lobectomy for predominantly diurnal seizures, experience a postoperative conversion from... 
Hippocampal sclerosis | Temporal lobe epilepsy | Seizure outcome | Epilepsy surgery | Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 1995, Volume 11, Issue 2, pp. 201 - 203
Copyright © 1995 Nature Publishing Group Ortrud K. Steinlein, John C. Mulley, Peter Propping, Robyn H. Wallace, Hilary A. Phillips, Grant R. Sutherland, Ingrid... 
Journal Article
Epilepsia, ISSN 0013-9580, 11/2012, Volume 53, Issue 11, pp. 1849 - 1859
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2012, Volume 90, Issue 6, pp. 1102 - 1107
Journal Article
Epilepsy Research, ISSN 0920-1211, 10/2019, Volume 156, pp. 106163 - 106163
The aetiology of self-limited epilepsy with centro-temporal spikes (SECTS) remains controversial and a strong genetic basis has long been presumed. The... 
Epigenetics | Self-limited epilepsy with centrotemporal spikes | Monozygotic twins | Index Medicus
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2013, Volume 45, Issue 7, pp. 825 - 830
Journal Article
by Allen, Andrew S and Berkovic, Samuel F and Cossette, Patrick and Delanty, Norman and Dlugos, Dennis and Eichler, Evan E and Epstein, Michael P and Glauser, Tracy and Goldstein, David B and Han, Yujun and Heinzen, Erin L and Hitomi, Yuki and Howell, Katherine B and Johnson, Michael R and Kuzniecky, Ruben and Lowenstein, Daniel H and Lu, Yi-Fan and Madou, Maura R. Z and Marson, Anthony G and Mefford, Heather C and Esmaeeli Nieh, Sahar and O'Brien, Terence J and Ottman, Ruth and Petrovski, Slavé and Poduri, Annapurna and Ruzzo, Elizabeth K and Scheffer, Ingrid E and Sherr, Elliott H and Yuskaitis, Christopher J and Abou-Khalil, Bassel and Alldredge, Brian K and Bautista, Jocelyn F and Boro, Alex and Cascino, Gregory D and Consalvo, Damian and Crumrine, Patricia and Devinsky, Orrin and Fiol, Miguel and Fountain, Nathan B and French, Jacqueline and Friedman, Daniel and Geller, Eric B and Glynn, Simon and Haut, Sheryl R and Hayward, Jean and Helmers, Sandra L and Joshi, Sucheta and Kanner, Andres and Kirsch, Heidi E and Knowlton, Robert C and Kossoff, Eric H and Kuperman, Rachel and McGuire, Shannon M and Motika, Paul V and Novotny, Edward J and Paolicchi, Juliann M and Parent, Jack M and Park, Kristen and Shellhaas, Renée A and Shih, Jerry J and Singh, Rani and Sirven, Joseph and Smith, Michael C and Sullivan, Joseph and Lin Thio, Liu and Venkat, Anu and Vining, Eileen P. G and Von Allmen, Gretchen K and Weisenberg, Judith L and Widdess-Walsh, Peter and Winawer, Melodie R and Epi4K Consortium and Epilepsy Phenome/Genome Project
Nature, ISSN 0028-0836, 2013, Volume 501, Issue 7466, pp. 217 - 221
Journal Article