X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (75) 75
humans (67) 67
grin2a (64) 64
epilepsy (55) 55
grin2a mutations (44) 44
clinical neurology (40) 40
male (40) 40
receptors, n-methyl-d-aspartate - genetics (40) 40
neurosciences (37) 37
female (36) 36
mutation (34) 34
aphasia (27) 27
encephalopathy (24) 24
genetic aspects (23) 23
schizophrenia (23) 23
glutamate (22) 22
analysis (18) 18
child (18) 18
de-novo mutations (18) 18
methyl aspartate (18) 18
genes (17) 17
seizures (17) 17
children (16) 16
genetic research (16) 16
genetics & heredity (16) 16
mutations (16) 16
adult (15) 15
animals (15) 15
genetics (15) 15
neurology (15) 15
nmda receptor (15) 15
electroencephalography (13) 13
epilepsy - genetics (13) 13
intellectual disability (12) 12
receptors, n-methyl-d-aspartate - metabolism (12) 12
sleep (12) 12
disorders (11) 11
genotype (11) 11
middle aged (11) 11
nmda (11) 11
polymorphism, single nucleotide - genetics (11) 11
spectrum (11) 11
subunit (11) 11
adolescent (10) 10
article (10) 10
child, preschool (10) 10
encephalopathies (10) 10
glun2a (10) 10
mice (10) 10
phenotype (10) 10
psychiatry (10) 10
research (9) 9
association (8) 8
autism (8) 8
case-control studies (8) 8
eeg (8) 8
expression (8) 8
gene expression (8) 8
genetic predisposition to disease (8) 8
genomics (8) 8
glutamic acid receptors (8) 8
n-methyl-d-aspartic acid receptors (8) 8
nmda receptors (8) 8
rolandic epilepsy (8) 8
synaptic plasticity (8) 8
aspartate (7) 7
behavioral sciences (7) 7
brain (7) 7
care and treatment (7) 7
childhood (7) 7
cohort studies (7) 7
focal epilepsy (7) 7
grin2b (7) 7
hippocampus (7) 7
landau-kleffner syndrome (7) 7
mutation - genetics (7) 7
nerve tissue proteins - genetics (7) 7
pediatrics (7) 7
speech (7) 7
biochemistry & molecular biology (6) 6
development and progression (6) 6
exome - genetics (6) 6
gene frequency (6) 6
genetic association studies (6) 6
genetic predisposition to disease - genetics (6) 6
glutamate-receptor (6) 6
hek293 cells (6) 6
long-term potentiation (6) 6
neurophysiology (6) 6
pharmacology & pharmacy (6) 6
proteins (6) 6
young adult (6) 6
antagonists (5) 5
cell biology (5) 5
childhood epilepsy (5) 5
cortex (5) 5
dysfunction (5) 5
epilepsy - diagnosis (5) 5
epilepsy, rolandic - genetics (5) 5
epileptic encephalopathy (5) 5
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Movement disorders : official journal of the Movement Disorder Society, ISSN 0885-3185, 3/2018, Volume 33, Issue 3, pp. 414 - 420
Journal Article
Movement disorders : official journal of the Movement Disorder Society, ISSN 0885-3185, 7/2018, Volume 33, Issue 6, pp. 992 - 999
Journal Article
Journal of the neurological sciences, ISSN 0022-510X, 4/2017, Volume 375, pp. 355 - 359
Caffeine is neuroprotective in animal models of PD and caffeine intake is inversely associated with the risk of Parkinson’s disease (PD). This association may... 
Progression | GRIN2A | Coffee | Creatine | Parkinson’s disease | Caffeine
Journal Article
Brain, ISSN 0006-8950, 09/2017, Volume 140, Issue 9, pp. 2337 - 2354
Journal Article
by Appenzeller, Silke and Balling, Rudi and Barisic, Nina and Baulac, Stéphanie and Caglayan, Hande and Craiu, Dana and De Jonghe, Peter and Depienne, Christel and Dimova, Petia and Djémié, Tania and Gormley, Padhraig and Guerrini, Renzo and Helbig, Ingo and Hjalgrim, Helle and Hoffman-Zacharska, Dorota and Jähn, Johanna and Klein, Karl Martin and Koeleman, Bobby and Komarek, Vladimir and Krause, Roland and Kuhlenbäumer, Gregor and Leguern, Eric and Lehesjoki, Anna-Elina and Lemke, Johannes R and Lerche, Holger and Linnankivi, Tarja and Marini, Carla and May, Patrick and Møller, Rikke S and Muhle, Hiltrud and Pal, Deb and Palotie, Aarno and Pendziwiat, Manuela and Robbiano, Angela and Roelens, Filip and Rosenow, Felix and Selmer, Kaja and Serratosa, Jose M and Sisodiya, Sanjay and Stephani, Ulrich and Sterbova, Katalin and Striano, Pasquale and Suls, Arvid and Talvik, Tiina and von Spiczak, Sarah and Weber, Yvonne and Weckhuysen, Sarah and Zara, Federico and Abou-Khalil, Bassel and Alldredge, Brian K and Andermann, Eva and Andermann, Frederick and Amron, Dina and Bautista, Jocelyn F and Berkovic, Samuel F and Bluvstein, Judith and Boro, Alex and Cascino, Gregory and Consalvo, Damian and Crumrine, Patricia and Devinsky, Orrin and Dlugos, Dennis and Epstein, Michael P and Fiol, Miguel and Fountain, Nathan B and French, Jacqueline and Friedman, Daniel and Geller, Eric B and Glauser, Tracy and Glynn, Simon and Haas, Kevin 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 Kuzniecky, Ruben and Lowenstein, Daniel H and McGuire, Shannon M and Motika, Paul V and Novotny, Edward J and Ottman, Ruth and Paolicchi, Juliann M and Parent, Jack and Park, Kristen and Poduri, Annapurna and Sadleir, Lynette and Scheffer, Ingrid E and Shellhaas, Renée A and Sherr, Elliott and Shih, Jerry J and Singh, Rani and Sirven, Joseph and Smith, Michael C and Sullivan, Joe and Thio, Liu Lin and ... and Epi4K Consortium and EuroEPINOMICS-RES Consortium and Epilepsy Phenome Genome Project and Epilepsy Phenome/Genome Project
The American Journal of Human Genetics, ISSN 0002-9297, 10/2014, Volume 95, Issue 4, pp. 360 - 370
Journal Article
Brain and Development, ISSN 0387-7604, 03/2018, Volume 40, Issue 3, pp. 205 - 210
Epilepsy-aphasia spectrum (EAS) are a group of epilepsy syndromes denoting an association between epilepsy, speech disorders and the EEG signature of... 
Aphasia | GRIN2A | Electrical status epilepticus during sleep | Mutation | Epilepsy | SLEEP | LANDAU-KLEFFNER SYNDROME | SPIKE-AND-WAVES | ROLANDIC EPILEPSY | PHENOTYPE | INCLUDING GRIN2A | CHILDHOOD | CLINICAL NEUROLOGY | ENCEPHALOPATHY | SRPX2 | GENES
Journal Article
Brain, ISSN 0006-8950, 01/2019, Volume 142, Issue 1, pp. 80 - 92
Strehlow et al. describe the largest cohort to date of individuals with GRIN2A-related disorders. The results reveal two phenotypic subgroups associated with... 
molecular genetics | GRIN2A MUTATIONS | VARIANTS | channelopathy | learning disability | spike-wave EEG | APHASIA | ENCEPHALOPATHY | GLUN2A | NMDA | childhood epilepsy | EPILEPSY | SPECTRUM | SUBUNIT
Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 03/2018, Volume 60, Issue 3, pp. 219 - 219
This commentary is on the original article by Currie et al. on pages 275–282 of this issue. 
PEDIATRICS | GRIN2A | CLINICAL NEUROLOGY | Electroencephalography | Language | Epilepsy, Rolandic | Humans
Journal Article
Epilepsia, ISSN 0013-9580, 06/2014, Volume 55, Issue 6, pp. 858 - 865
Journal Article
Journal Article