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Samuel F Berkovic

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Credit Name
Samuel F Berkovic
Full Name
Berkovic, Samuel F
 
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ORCID
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Publications

Results 181-200 of 328 (Search time: 0.009 seconds).

Publication YearTitleAuthor(s)
1817-Jun-2013Etiology of hippocampal sclerosis: evidence for a predisposing familial morphologic anomaly.Tsai, Meng-Han; Pardoe, Heath R; Perchyonok, Yuliya ; Fitt, Gregory J ; Scheffer, Ingrid E ; Jackson, Graeme D ; Berkovic, Samuel F 
18226-Apr-2013Expression of the transmembrane lysosomal protein SCARB2/Limp-2 in renin secretory granules controls renin release.Lee, D ; Desmond, Michael J; Fraser, S A; Katerelos, M ; Gleich, Kurt; Berkovic, Samuel F ; Power, David Anthony
18316-Apr-2013Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26.Klein, Karl Martin; Bromhead, Catherine J; Smith, Katherine R; O'Callaghan, Christopher J ; Corcoran, Susan J; Heron, Sarah E; Iona, Xenia; Hodgson, Bree L; McMahon, Jacinta M; Lawrence, Kate M; Scheffer, Ingrid E ; Dibbens, Leanne M; Bahlo, Melanie; Berkovic, Samuel F 
421-Mar-2013Genetics of febrile seizure subtypes and syndromes: a twin study.Eckhaus, Jazmin; Lawrence, Kate M; Helbig, Ingo; Bui, Minh; Vadlamudi, Lata; Hopper, John L; Scheffer, Ingrid E ; Berkovic, Samuel F 
513-Mar-2013Genetics of epilepsy syndromes in families with photosensitivity.Taylor, Isabella; Berkovic, Samuel F ; Scheffer, Ingrid E 
66-Mar-2013Recent advances in the molecular genetics of epilepsy.Hildebrand, Michael S ; Dahl, Hans-Henrik M; Damiano, John Anthony; Smith, Richard J H; Scheffer, Ingrid E ; Berkovic, Samuel F 
728-Feb-2013'North Sea' progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation.Boissé Lomax, Lysa; Bayly, Marta A; Hjalgrim, Helle; Møller, Rikke S; Vlaar, Annemarie M; Aaberg, Kari M; Marquardt, Iris; Gandolfo, Luke C; Willemsen, Michèl; Kamsteeg, Erik-Jan; O'Sullivan, John D; Korenke, G Christoph; Bloem, Bastiaan R; de Coo, Irenaeus F; Verhagen, Judith M A; Said, Ines; Prescott, Trine; Stray-Pedersen, Asbjørg; Rasmussen, Magnhild; Vears, Danya F; Lehesjoki, Anna-Elina; Corbett, Mark A; Bahlo, Melanie; Gecz, Jozef; Dibbens, Leanne M; Berkovic, Samuel F 
81-Feb-2013Abnormal Processing of Autophagosomes in Transformed B Lymphocytes from SCARB2-Deficient Subjects.Gleich, Kurt; Desmond, Michael J; Lee, Darren; Berkovic, Samuel F ; Dibbens, Leanne M; Katerelos, Marina ; Bayly, Marta A; Fraser, Scott A; Martinello, Paul; Vears, Danya F; Mount, Peter; Power, David Anthony
97-Jan-2013Clinical genetic study of the epilepsy-aphasia spectrum.Tsai, Meng-Han; Vears, Danya F; Turner, Samantha J; Smith, Robert L; Berkovic, Samuel F ; Sadleir, Lynette G; Scheffer, Ingrid E 
107-Jan-2013Siblings with refractory occipital epilepsy showing localized network activity on EEG-fMRI.Carney, Patrick W ; Harvey, A Simon; Berkovic, Samuel F ; Jackson, Graeme D ; Scheffer, Ingrid E 
113-Dec-2012Cortical excitability and refractory epilepsy: a three-year longitudinal transcranial magnetic stimulation study.Badawy, Radwa A B; Jackson, Graeme D ; Berkovic, Samuel F ; Macdonell, Richard A L 
1220-Nov-2012Do mutations in SCN1B cause Dravet syndrome?Kim, Young Ok; Dibbens, Leanne M; Marini, Carla; Suls, Arvid; Chemaly, Nicole; Mei, Davide; McMahon, Jacinta M; Iona, Xenia; Berkovic, Samuel F ; De Jonghe, Peter; Guerrini, Renzo; Nabbout, Rima; Scheffer, Ingrid E 
131-Nov-2012Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.Arsov, Todor; Mullen, Saul A ; Rogers, Sue; Phillips, A Marie; Lawrence, Kate M; Damiano, John Anthony; Goldberg-Stern, Hadassa; Afawi, Zaid; Kivity, Sara; Trager, Chantal; Petrou, Steven; Berkovic, Samuel F ; Scheffer, Ingrid E 
1425-Oct-2012Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.Arsov, Todor; Mullen, Saul A ; Damiano, John Anthony; Lawrence, Kate M; Huh, Linda L; Nolan, Melinda; Young, Helen ; Thouin, Anaïs; Dahl, Hans-Henrik M; Berkovic, Samuel F ; Crompton, Douglas E; Sadleir, Lynette G; Scheffer, Ingrid E 
157-Aug-2012Evidence for genetic factors in vasovagal syncope: a twin-family study.Klein, Karl Martin; Xu, San San ; Lawrence, Kate M; Fischer, Alexandra; Berkovic, Samuel F 
1610-Jul-2012Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum.Klein, Karl Martin; O'Brien, Terence J; Praveen, Kavita; Heron, Sarah E; Mulley, John C; Foote, Simon; Berkovic, Samuel F ; Scheffer, Ingrid E 
1728-Mar-2012The frontal lobe in absence epilepsy: EEG-fMRI findings.Carney, Patrick W ; Masterton, Richard A J; Flanagan, D; Berkovic, Samuel F ; Jackson, Graeme D 
183-Mar-2012Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.Carranza Rojo, Daniel; Harvey, A Simon; Iona, Xenia; Dibbens, Leanne M; Damiano, John Anthony; Arsov, Todor; Gill, Deepak S; Freeman, Jeremy L; Leventer, Richard J; Vincent, Angela; Berkovic, Samuel F ; McMahon, Jacinta M; Scheffer, Ingrid E 
195-Jan-2012Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes.Vears, Danya F; Tsai, Meng-Han; Sadleir, Lynette G; Grinton, Bronwyn E; Lillywhite, Leasha M; Carney, Patrick W ; Harvey, A Simon; Berkovic, Samuel F ; Scheffer, Ingrid E 
2021-Oct-2011Inter-session repeatability of cortical excitability measurements in patients with epilepsy.Badawy, Radwa A B; Jackson, Graeme D ; Berkovic, Samuel F ; Macdonell, Richard A L