-
1
-
-
78649995149
-
Clinical experience and laboratory investigations in patients with anti-NMDAR encephalitis
-
Dalmau J, Lancaster E, Martinez-Hernandez E, et al. Clinical experience and laboratory investigations in patients with anti-NMDAR encephalitis. Lancet Neurol 2011; 10: 63–74.
-
(2011)
Lancet Neurol
, vol.10
, pp. 63-74
-
-
Dalmau, J.1
Lancaster, E.2
Martinez-Hernandez, E.3
-
2
-
-
84892483602
-
N-methyl-d-aspartate receptor antibody-associated movement disorder without encephalopathy
-
Hacohen Y, Dlamini N, Hedderly T, et al. N-methyl-d-aspartate receptor antibody-associated movement disorder without encephalopathy. Dev Med Child Neurol 2014; 56: 190–93.
-
(2014)
Dev Med Child Neurol
, vol.56
, pp. 190-193
-
-
Hacohen, Y.1
Dlamini, N.2
Hedderly, T.3
-
3
-
-
84927513029
-
Movement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies
-
Mohammad SS, Fung VS, Grattan-Smith P, et al. Movement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies. Mov Disord 2014; 29: 1539–42.
-
(2014)
Mov Disord
, vol.29
, pp. 1539-1542
-
-
Mohammad, S.S.1
Fung, V.S.2
Grattan-Smith, P.3
-
4
-
-
52649109254
-
The distinctive movement disorder of ovarian teratoma-associated encephalitis
-
Kleinig TJ, Thompson PD, Matar W, et al. The distinctive movement disorder of ovarian teratoma-associated encephalitis. Mov Disord 2008; 23: 1256–61.
-
(2008)
Mov Disord
, vol.23
, pp. 1256-1261
-
-
Kleinig, T.J.1
Thompson, P.D.2
Matar, W.3
-
5
-
-
84961189699
-
Symptomatic treatment of children with anti-NMDAR encephalitis
-
Mohammad SS, Jones H, Hong M, et al. Symptomatic treatment of children with anti-NMDAR encephalitis. Dev Med Child Neurol 2016; 58: 376–84.
-
(2016)
Dev Med Child Neurol
, vol.58
, pp. 376-384
-
-
Mohammad, S.S.1
Jones, H.2
Hong, M.3
-
6
-
-
84883463114
-
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
-
Lemke JR, Lal D, Reinthaler EM, et al. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nat Genet 2013; 45: 1067–72.
-
(2013)
Nat Genet
, vol.45
, pp. 1067-1072
-
-
Lemke, J.R.1
Lal, D.2
Reinthaler, E.M.3
-
7
-
-
84883446382
-
GRIN2A mutations cause epilepsy-aphasia spectrum disorders
-
Carvill GL, Regan BM, Yendle SC, et al. GRIN2A mutations cause epilepsy-aphasia spectrum disorders. Nat Genet 2013; 45: 1073–76.
-
(2013)
Nat Genet
, vol.45
, pp. 1073-1076
-
-
Carvill, G.L.1
Regan, B.M.2
Yendle, S.C.3
-
8
-
-
84883462975
-
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
-
Lesca G, Rudolf G, Bruneau N, et al. GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nat Genet 2013; 45: 1061–66.
-
(2013)
Nat Genet
, vol.45
, pp. 1061-1066
-
-
Lesca, G.1
Rudolf, G.2
Bruneau, N.3
-
9
-
-
84878254691
-
NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease
-
Paoletti P, Bellone C, Zhou Q. NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease. Nat Rev Neurosci 2013; 14: 383–400.
-
(2013)
Nat Rev Neurosci
, vol.14
, pp. 383-400
-
-
Paoletti, P.1
Bellone, C.2
Zhou, Q.3
-
10
-
-
84862297282
-
Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function
-
Won H, Lee HR, Gee HY, et al. Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function. Nature 2012; 486: 261–65.
-
(2012)
Nature
, vol.486
, pp. 261-265
-
-
Won, H.1
Lee, H.R.2
Gee, H.Y.3
-
11
-
-
84899671093
-
Anti-N-Methyl-d-Aspartate (NMDA) receptor encephalitis: an unusual cause of autistic regression in a toddler
-
Scott O, Richer L, Forbes K, et al. Anti-N-Methyl-d-Aspartate (NMDA) receptor encephalitis: an unusual cause of autistic regression in a toddler. J Child Neurol 2014; 29: 691–94.
-
(2014)
J Child Neurol
, vol.29
, pp. 691-694
-
-
Scott, O.1
Richer, L.2
Forbes, K.3
-
12
-
-
79959997661
-
Late onset autism and anti-NMDA-receptor encephalitis
-
Creten C, van der Zwaan S, Blankespoor RJ, et al. Late onset autism and anti-NMDA-receptor encephalitis. Lancet 2011; 378: 98.
-
(2011)
Lancet
, vol.378
, pp. 98
-
-
Creten, C.1
van der Zwaan, S.2
Blankespoor, R.J.3
-
13
-
-
84930029489
-
N-methyl-d-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in children
-
Wright S, Hacohen Y, Jacobson L, et al. N-methyl-d-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in children. Arch Dis Child 2015; 100: 521–26.
-
(2015)
Arch Dis Child
, vol.100
, pp. 521-526
-
-
Wright, S.1
Hacohen, Y.2
Jacobson, L.3
-
14
-
-
85020399458
-
Earlier treatment of NMDAR antibody encephalitis in children results in a better outcome
-
Byrne S, Walsh C, Hacohen Y, et al. Earlier treatment of NMDAR antibody encephalitis in children results in a better outcome. Neurol Neuroimmunol Neuroinflamm 2015; 2: e130.
-
(2015)
Neurol Neuroimmunol Neuroinflamm
, vol.2
-
-
Byrne, S.1
Walsh, C.2
Hacohen, Y.3
|