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Snezana Maljevic
Snezana Maljevic
Unknown affiliation
Verified email at florey.edu.au
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Cited by
Cited by
Year
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
K Haug, M Warnstedt, AK Alekov, T Sander, A Ramírez, B Poser, ...
Nature genetics 33 (4), 527-532, 2003
4702003
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
YG Weber, A Storch, TV Wuttke, K Brockmann, J Kempfle, S Maljevic, ...
The Journal of clinical investigation 118 (6), 2157-2168, 2008
3892008
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1
A Suls, P Dedeken, K Goffin, H Van Esch, P Dupont, D Cassiman, ...
Brain 131 (7), 1831-1844, 2008
3802008
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
M Muona, SF Berkovic, LM Dibbens, KL Oliver, S Maljevic, MA Bayly, ...
Nature genetics 47 (1), 39-46, 2015
3122015
The new anticonvulsant retigabine favors voltage-dependent opening of the Kv7. 2 (KCNQ2) channel by binding to its activation gate
TV Wuttke, G Seebohm, S Bail, S Maljevic, H Lerche
Molecular pharmacology 67 (4), 1009-1017, 2005
3102005
De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
S Syrbe, U Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ...
Nature genetics 47 (4), 393-399, 2015
2822015
A mutation in the GABAA receptor α1‐subunit is associated with absence epilepsy
S Maljevic, K Krampfl, J Cobilanschi, N Tilgen, S Beyer, YG Weber, ...
Annals of Neurology: Official Journal of the American Neurological …, 2006
2642006
Dominant‐negative effects of KCNQ2 mutations are associated with epileptic encephalopathy
G Orhan, M Bock, D Schepers, EI Ilina, SN Reichel, H Löffler, N Jezutkovic, ...
Annals of neurology 75 (3), 382-394, 2014
2582014
Ion channels in genetic epilepsy: from genes and mechanisms to disease-targeted therapies
J Oyrer, S Maljevic, IE Scheffer, SF Berkovic, S Petrou, CA Reid
Pharmacological reviews 70 (1), 142-173, 2018
2572018
Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy
Y Liao, L Deprez, S Maljevic, J Pitsch, L Claes, D Hristova, A Jordanova, ...
Brain 133 (5), 1403-1414, 2010
2032010
Nervous system KV7 disorders: breakdown of a subthreshold brake
S Maljevic, TV Wuttke, H Lerche
The Journal of physiology 586 (7), 1791-1801, 2008
1932008
SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain
Y Liao, AK Anttonen, E Liukkonen, E Gaily, S Maljevic, S Schubert, ...
Neurology 75 (16), 1454-1458, 2010
1792010
Phenotypic spectrum of GABRA1 From generalized epilepsies to severe epileptic encephalopathies
K Johannesen, C Marini, S Pfeffer, RS Møller, T Dorn, CE Niturad, ...
Neurology 87 (11), 1140-1151, 2016
1452016
KV7 channelopathies
S Maljevic, TV Wuttke, G Seebohm, H Lerche
Pflügers Archiv-European Journal of Physiology 460, 277-288, 2010
1432010
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect
YG Weber, C Kamm, A Suls, J Kempfle, K Kotschet, R Schüle, TV Wuttke, ...
Neurology 77 (10), 959-964, 2011
1192011
Mutations in GABRB3 From febrile seizures to epileptic encephalopathies
RS Møller, TV Wuttke, I Helbig, C Marini, KM Johannesen, EH Brilstra, ...
Neurology 88 (5), 483-492, 2017
1132017
Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia
N Schwarz, A Hahn, T Bast, S Müller, H Löffler, S Maljevic, E Gaily, I Prehl, ...
Journal of neurology 263, 334-343, 2016
992016
SCN1A gain of function in early infantile encephalopathy
G Berecki, A Bryson, J Terhag, S Maljevic, EV Gazina, SL Hill, S Petrou
Annals of neurology 85 (4), 514-525, 2019
972019
Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy
MA Corbett, ST Bellows, M Li, R Carroll, S Micallef, GL Carvill, CT Myers, ...
Neurology 87 (19), 1975-1984, 2016
952016
Molecular analysis of the A322D mutation in the GABAA receptor α1‐subunit causing juvenile myoclonic epilepsy
K Krampfl, S Maljevic, P Cossette, E Ziegler, GA Rouleau, H Lerche, ...
European Journal of Neuroscience 22 (1), 10-20, 2005
932005
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