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Jillian M Cameron

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Credit Name
Jillian M Cameron
Full Name
Cameron, Jillian M
 
Department
 
ORCID
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Publications

Results 1-6 of 6 (Search time: 0.005 seconds).

Publication YearTitleAuthor(s)
12024Exploring individual fixel-based white matter abnormalities in epilepsy.Mito, Remika; Pedersen, Mangor; Pardoe, Heath; Parker, Donna; Smith, Robert E; Cameron, Jillian M ; Scheffer, Ingrid E ; Berkovic, Samuel F ; Vaughan, David N; Jackson, Graeme D 
224-Aug-2023ILAE Genetics Literacy Series: Progressive Myoclonus Epilepsies.Cameron, Jillian M ; Ellis, Colin A; Berkovic, Samuel F 
3Aug-2023IRF2BPL: A new genotype for progressive myoclonus epilepsies.Costa, Cinzia; Oliver, Karen L; Calvello, Carmen; Cameron, Jillian M ; Imperatore, Valentina; Tonelli, Laura; Colavito, Davide; Franceschetti, Silvana; Canafoglia, Laura; Berkovic, Samuel F ; Prontera, Paolo
4Jul-2023Recognition and Epileptology of Protracted CLN3 Disease.Cameron, Jillian M ; Damiano, John A; Grinton, Bronwyn; Carney, Patrick W ; McKelvie, Penny; Silbert, Peter; Lawn, Nicholas; Scheffer, Ingrid E ; Oliver, Karen L; Hildebrand, Michael S ; Berkovic, Samuel F 
51-Apr-2021Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.Courage, Carolina; Oliver, Karen L; Park, Eon Joo; Cameron, Jillian M ; Grabińska, Kariona A; Muona, Mikko; Canafoglia, Laura; Gambardella, Antonio; Said, Edith; Afawi, Zaid; Baykan, Betul; Brandt, Christian; di Bonaventura, Carlo; Chew, Hui Bein; Criscuolo, Chiara; Dibbens, Leanne M; Castellotti, Barbara; Riguzzi, Patrizia; Labate, Angelo; Filla, Alessandro; Giallonardo, Anna T; Berecki, Geza; Jackson, Christopher B; Joensuu, Tarja; Damiano, John A; Kivity, Sara; Korczyn, Amos; Palotie, Aarno; Striano, Pasquale; Uccellini, Davide; Giuliano, Loretta; Andermann, Eva; Scheffer, Ingrid E ; Michelucci, Roberto; Bahlo, Melanie; Franceschetti, Silvana; Sessa, William C; Berkovic, Samuel F ; Lehesjoki, Anna-Elina
6Jul-2019Encephalopathies with KCNC1 variants: genotype-phenotype-functional correlations.Cameron, Jillian M ; Maljevic, Snezana; Nair, Umesh; Aung, Ye Htet; Cogné, Benjamin; Bézieau, Stéphane; Blair, Edward; Isidor, Bertrand; Zweier, Christiane; Reis, André; Koenig, Mary Kay; Maarup, Timothy; Sarco, Dean; Afenjar, Alexandra; Huq, A H M Mahbubul; Kukolich, Mary; Billette de Villemeur, Thierry; Nava, Caroline; Héron, Bénédicte; Petrou, Steven; Berkovic, Samuel F